800 Bio-Tech, Clinical Research jobs

Job Description:Required Qualification and Experience: M.Tech (Chemical Engineering) 3-6 years and B.Tech 6-9 years of relevant experience Preferred Industry Exposure: Pharmaceutical / Agro sciences Job location: Bangalore Key duties Designing and execute experimental protocols in lab. Engineering data generation to support scale-up activities. Exposure to unit operations such as filtration, drying, crystallization, distillation etc. Prepare process safety assessment reports to support scale-up activities. Provide technical support to scale-up campaigns in kilo and pilot plant. Hands on experience in handling Automated lab reactors, setting up experiments to generate data etc. Proficient in Dynochem, Visimix, DoE (minitab/Design expert) and other simulation softwares etc. Issue technical and investigation reports Support, monitoring and analysis of process performance and product quality data on a periodic basis. Additional requirements: Assisting the facility establishment programs for the chemical development group. Able to work with little or no guidance or support to improve equipment and processes. Able to assist multiple projects at the same time. Other tasks as required to assist Technical Operations, other divisions, and the company. Work with customers, Project Managers, Tech Ops, Operations, Engineering and Maintenance to coordinate activities in accordance with planned schedules, customer specifications and establish quality standards.

Job Description:JD - Bio Statistician - Clinical - BA/BE

Job Description:JD - QA Clinical - Clinical Quality Assurance JD - QA Bioanalytical - Bioanalytical Quality Assurance

Job Description:1.Coordinate with production team day to day production activities 2.Assist with the development, documentation, and implementation of procedures and standards. 3.Analyze data of several batches and interpret 4.Oversee assistants as required by division structure and workload 5.Routine clerical duties to support division activities and equipment. May include supervision of others performing these duties. 6.Monitor quality, service, and delivery issues, and take corrective actions as needed 7.Must prepare buffers and carry out routine batches as per MFR. 8.Monitor batches and take necessary actions as per SOP. 9.Coordinate with QA and Marketing in shipment of material. Note: This position is for Male Candidate only.

Job Description:Candidate with 0-2 years of relevant industrial experience working particularly in the quality assurance division. Good grasp of regulatory procedures is essential. Experience with ISO 9001:2000 or ISO 13485:2003 and ISO 18001 is desirable. Candidate would be in charge of quality assurance programmes related to the development and production of native antigens, antibodies, cell derived antigens and recombinant proteins. Qualification: B.Pharm / B.Sc.

Job Description:Regenerative Medical Services Pvt Ltd is hiring for Associate Medical Communication &amp amp amp Research Responsibilities- a) Preparing case studies, medical abstract writing, medical write - ups for media publishing and Newsletter b)Preparing Manuscript for publishing c)Preparing market reports and presentation d)Technical content build up for online as well as offline media, for national &amp amp amp international conferences, government offices, e) Preparing content for associated doctors, hospitals, sales &amp amp amp BD team, patient communication f) Coordinating with R&amp amp amp D, Lab, clinical research team, IPR dept g)Conducting continuous research for content improvement Desired Candidate profile- Masters in Science / Pharmacy / Biotechnology Minimum 2 years experience in Research &amp amp amp Development Feman job-seeker only Good command on English Research oriented attitude To apply, send your CV to shweta.gharat@regrow.in&amp amp nbsp Our website- www.regrow.in / www.babycell.in Regards, Shweta

Job Description:Dear Candidate, Greetings From RESOLVE MEDICODE!! We are hiring Fresher - Medical Coder, Medical Coding is the process of converting Verbal Descriptions into numeric or alpha numeric by using ICD 10-CM, CPT &amp amp amp HCPCS. Medical Coders should review the documentation contain patients medical records and translate it into universally accepted industry-standard code. Pay Scale: 10,000 to 18,000 (Fresher) &amp amp amp upto 50,000(Experienced) per month with assured career growth (Incentives &amp amp amp Benefits as per Corporate Standards). Benefits - Weekends off Cab Food/Incentives Eligibility : Nursing, Pharmacy, Botany, Zoology, Microbiology, Biochemistry, Biotechnology, Plant Botany &amp amp amp Biotechnology, Advance Zoology &amp amp amp Biotechnology, Psychology, Nutrition &amp amp amp Dietetics, Diploma courses in Allied health Sciences etc., Requirements: Candidate should be from Medical/Paramedical Life Science Allied Health Sciences Strong knowledge in Anatomy, Physiology and Pathology. For Details Suchithra Recruitment Associate 7500052460 http://medi-code.in/

Job Description:Outstanding Knowledge of ERP Microsoft Dynamics Navision

Job Description:Secondary sales achieving secondary sales targets through order booking and POB execution. Communication of various schemes operating and being a channel between distributors and retailers. Generating new orders and sales in their territory. Ensuring product awareness and visibility through displays and other merchandising, posters etc. Day to day sales reporting. Effective query handling and customer satisfaction.

Job Description:Preparing and drafting contracts, agreements, other documents. Filing police complaints, follow-up with advocates. Preparing and drafting replies of complaints, Consumer cases and other litigations. Keeps abreast of the latest developments in legislation and regulations. Representing Company at various forums Such other work as may be assigned in the legal division. Develops standard legal templates, documents and contracts

Job Description:&amp amp nbsp hat are my duties? 1. Maintain network to customers, business experts and other subject matter experts to understand business data analytics requirements and identify data analytics driven business opportunities 2. Conduct data exploration and identify relevant data sets and new relations in data 3. Identify further data requirements and integrate such data 4. Develop and test prototypes in an industrial environment, validate and communicate results to answer targeted business questions 5. Develop marketable (product grade quality) analytic models, configure and deploy algorithms, selects optimal tool and define visualization method/tool to display results 6. Set up visualization systems to display results in most appropriate way based on cognitive science 7. Define and provide requirements to IT infrastructure 8. Determine sustainable processes to support fast growing data volumes and making sure that of data quality and data accessibility together with the data architect 9. Collaborate with Enterprise IT, service and product business units to keep-up analytics models 10.Implement and manage big data analytics projects and present results to stakeholders inside and outside the company 11.Explore new innovative technologies and open source projects What do I need to qualify for the job? 1. Degree in quantitative discipline (e.g. Mathematics, Computer Science, Electrical Engineering, etc.) 2. Strong Analytical skills 3. Sound knowledge on statistics/stochastics 4. Hands-on programming experience (of minimum one year) 5. Proficiency in at least one programming language (e.g. SAS, R, Matlab, C, C++, Java, Python, PHP, JavaScript) 6. Experience in working with large data sets, incl. SQL coding (of minimum 6 months) 7. Experience in data integration, data transformation, evaluation of data quality and data cleansing 8. Hands-on experience in implementing analytical algorithms (e.g. prediction models) 9. Generally IT-savvy (able to solve day-to-day IT challenges independently) 10.Experience working with SAS Tools (Enterprise Guide, Enterprise Miner, Data Integration Studio, Visual Analytics) is an added advantage 11.Good problem solving skills 12.Good communication skills (verbal and written) 13.Strong project management skills 14.Good time management and organizational capabilities 15.Open to travel for business 16.Knowledge in MS Excel, Access, PowerPoint

Job Description:Opportunity: This is a tremendous opportunity to learn and develop skills and experience that will allow you to grow. You will work in fun, friendly and organically growing organization that values and rewards its employees. The opportunity to grow individually, within the team and the organization is tremendous. WALK-IN INTERVIEWS: Interview Address: Advantmed, 4th Floor - 402, Pinnacle Business Park, Corporate Road, Prahaladnagar, Ahmedabad, Gujarat. Requirement: Education: B.Pharm / M.Pharm /D.Pharm / Biomedical Engineering or B.Sc. / M.Sc (Biochemistry / Biotechnology / Biological Science / Medicinal Chemistry / Microbiology Experience: Fresher Below are the details about the requirement: Job Title: Junior Associate - Medical Coding Job Location: Ahmedabad, Gujarat. Shift Timings: 8:00 AM 5.30 PM Working Days: 5 Days [Monday to Friday], Work on Saturdays &amp amp amp Earn Extra Salary structure: Outstanding Salary Package + Attractive Bonus + Performance Incentives + Outstanding work culture Fun Fridays Cultural Celebrations &amp amp amp Lots more. Responsibilities: Duties include but not limited to: Follow project specific guide lines without any deviation. Performs assigned tasks / completes targets with speed and accuracy as per client requirements. Study medical records of U.S. patients as provided and enter relevant correct codes for patients medical conditions on companys internal portal. Perform work as assigned. Requirements: Minimum Bachelor' s in Pharmacy or Science and/or Master' s in Pharmacy or Science with above-average English communication skills. Good skills in reading handwritten Notes / Doctors prescription. Good knowledge of medical terms and terminologies. Basic knowledge of computer (MS Office) Ability to pay attention to detail. Ability to work in a team. Willingness and flexibility to work for 6/7 Days a week (as required).

Job Description:Secondary sales achieving secondary sales targets through order booking and POB execution. Communication of various schemes operating and being a channel between distributors and retailers. Generating new orders and sales in their territory. Ensuring product awareness and visibility through displays and other merchandising, posters etc. Day to day sales reporting. Effective query handling and customer satisfaction.

Job Description:PF JD Below Strong English writing and communication skills. Knowledge of Microsoft Office packages to include Outlook, Word, PowerPoint and Excel are essential. Great attention to detail and will take leadership over the divisions filing and archiving. Must be very organised, self-driven and highly motivated. Must be able to understand and follow above-average documentation practices. Previous experience at managing high volumes of documentation paper or electronic would obviously be favourable. Previous work in a clinical or Biometrics setting would also be favourable. Ability to work in a fast-paced setting with many interruptions.

Job Description:Walk-in for medical coding 2017 to 2018 passed out job-seekers! Great opportunity for freshers to work in COIMBATORE! A better realistic future awaits you in the field of coding and billing.

Job Description:Patients' Medical Information into standard Diagnosis codes(ICD-10CM) and Procedure Codes(CPT). Requirements: Age should be below 30. Good Communication skill. Benefits- Weekends off/Cab/Food/Incentives Contact: HR Karthik - 7200273695 Core2Code

Job Description:To make sure that the seemless functioning of the medical equipments in all the centers in the respective region To install medical equipment in the new centers and existing centers Prepare annual inventory plan of the medical equipments &amp amp keep track of store

Job Description:Implementation, Scheduling and Management of processes involved in Planned Preventive Maintenance. Corrective Maintenance including routine corrective upkeep, breakdown and emergency upkeep. etc

Job Description:Advertisement No.1928 Dt.15-05-2018 Pay Scale: This engagement is on a fixed remuneration (as per Government of Odisha norms) per teaching hour Prescribed qualification :M.Sc. in Zoology / Life Sciences / Biochemistry / Biotechnology / Microbiology having either NET / Ph.D. Date of Interview :27-05-2018 Time of Interview :10.30 am 1.30 pm Venue: The Office of the Vice-Chancellor Ravenshaw University Cuttack (Odisha) For more details:http://www.ravenshawuniversity.ac.in/Content/Advertisement_Guest.pdf &amp amp nbsp

Job Description:Hi Greetings from Technosoft Corporation !! About Technosoft: Technosoft is an integrated Information Technology (IT) and Business Process Management (BPM) solutions provider. Our collaborative culture and work environment helps attract and retain exceptional talent which is a key ingredient to address our clients needs, and help drive our sustained growth. Our biggest differentiators include: A Focused Service Portfolio Customer-Centric Approach Outcome-Based Model Exceptional Talent Culture of Curiosity and Confidence Technosoft has approximately 3,600+ employees worldwide. Our global footprint spans across North America, India, UK, Australia and New Zealand, and the Middle East. Our vision is to be partner and employer of choice in our chosen segment. For more information, visit us at www.technosoftcorp.com Specialties: IT Consulting, BPM services, Healthcare IT, Data Sciences, Mobility, Global In-house Centers, Professional Staffing. Immediate requirement for Clinical Process Trainee in Thane Location. Contact : Prasanna(7989790257) Forward Your Updated CV to: prasanna. technosoft@gmail.com Job Description : Experience 6 mnths - 4 Years (In clinical research) Skills required - CRA knowledge, CRC knowledge, Patient Data knowledge, ICH - GCP, ICF, Adverse Events/ SAEs, site monitoring, remote site monitoring knowledge. (eTMF - experience - not mandatory but preferred). PURPOSE: Provide project related assistance for assigned complex project(s), sites and project teams. Make sure that all work is conducted in accordance with SOPs, policies and practices, above-average clinical practices and applicable regulatory requirements and meets quality and timeline metrics. DUTIES : Perform complex processes and tasks that eventually result in high quality deliverables that are completed according to service level agreements (SLAs) and within project timelines Establish and keep-up effective project/ site communications Create and keep-up relevant project documents Make sure that accurate completion and upkeep of internal systems, databases, tracking tools, timelines and project plans with project specific information Participate in document management (creation, review, upkeep, storage, as applicable) REQUIRED KNOWLEDGE, SKILLS AND ABILITIES Good knowledge of applicable clinical research regulatory requirements i.e., ICH GCP and relevant local laws, regulations and guidelines Strong written and verbal communication skills including above-average command of English language Results and detail-oriented approach to work delivery and output Good problem solving skills Good planning, time management and prioritization skills Attention to detail and accuracy in work Good software and computer skills, including MS Office applications including but not limited to Microsoft Word, Excel and PowerPoint Ability to establish and keep-up effective working relationships with coworkers, managers and clients. Proven ability to work on multiple projects balancing competing priorities Ability to coach/ mentor junior colleagues Schedule interview : If above Requirements matches to your profile can send your updated CV to : prasanna .technosoft@gmail.com and reach at 7989790257 (drop me a text message)* Note : Ignore, if JD not matches to your profile &amp Do Refer to your Friends &amp Colleagues Regards Prasanna HR-TA 7989790257 prasanna .technosoft@gmail.com

Job Description:Medical reviewers examine medical documents for accuracy, such as looking at patient records and insurance paperwork. They can work in medical facilities or for independent firms. Call/watsapp- 9566120230

Job Description:Job Description To develop new business relationships, generate and negotiate new income for Organiz Presenting Companies capability as CRO to potential clients through direct communication in face to face meetings, telephone calls and emails In charge of lead generation and related activities, primarily to build the new business portfolio for the business In charge of selling pre-clinical services globally to all sectors of research- pharma, agro, biotech etc. Deliver RFPs on a timely basis, making sure that month wise closure of sales numbers Cross functional people interaction delivering on business units revenue numbers Client management o Managing client visits on site at CRO Company o Attending conferences, managing visits to client sites independently Proposals and pricing in discussion with the technical team Pricing negotiations with clients Presentations and strategy/account planning for the business Operational support internally to manage billing cycle International and domestic travel when required for business purpose To develop new business relationships, generate and negotiate new income for Organization Presenting companies capability as CRO to potential clients through direct communication in face to face meetings, telephone calls and emails In charge of lead generation and related activities, primarily to build the new business portfolio for the business In charge of selling pre-clinical services globally to all sectors of research- pharma, agro, biotech etc. Deliver RFPs on a timely basis, making sure that month wise closure of sales numbers Cross functional people interaction delivering on business units revenue numbers Client management

Job Description:Hands-on experience in HPLC analysis of proteins and experience with one or more of the following analytical techniques is desired: mass spectrometry, isoelectric focusing, or automated. 8838230950

Job Description:Analytical methods development of Raw Materials / Finished Formulations. Carry out stability testing &amp amp establishing shelf life of formulations (Related Substance, Assay, Content Uniformity, Dissolution &amp amp Dissolution profile) by HPLC / GC / UV etc.

Job Description:Hi Greetings from Technosoft Corporation !! About Technosoft: Technosoft is an integrated Information Technology (IT) and Business Process Management (BPM) solutions provider. Our collaborative culture and work environment helps attract and retain exceptional talent which is a key ingredient to address our clients needs, and help drive our sustained growth. Our biggest differentiators include: A Focused Service Portfolio Customer-Centric Approach Outcome-Based Model Exceptional Talent Culture of Curiosity and Confidence Technosoft has approximately 3,600+ employees worldwide. Our global footprint spans across North America, India, UK, Australia and New Zealand, and the Middle East. Our vision is to be partner and employer of choice in our chosen segment. For more information, visit us at www.technosoftcorp.com Specialties: IT Consulting, BPM services, Healthcare IT, Data Sciences, Mobility, Global In-house Centers, Professional Staffing. Immediate requirement for "Clinical Process Trainee" in Thane (Mumbai) Location. Contact : Vani B (9182991774) Forward Your Updated CV to : Vani.B@technosoftcorp.com Job Description : Experience 6 Months - 4 Years (Clinical Process Trainee) Notice Period: Immediate Should be flexible with Thane location Skills required - Good Communication Skills Verbal + Written / Excel Skill Roles &amp Responsibilities: Complete appropriate role-specific training to perform job duties Under supervision, perform assigned administrative tasks to support team members with project execution (examples of such tasks include but not limited to running system reports, keep-uping minutes of meeting, put-together and distributing status reports, creating and keep-uping study documents, etc.) Under supervision, assist in updating and keep-uping systems within project timelines and per project plans The staff will review the PDF file and locate the appropriate fields for entry into an excel database. Double-data entry will be used for this service. A comparison will be performed between the initial entry and the double data entry. The staff will be in charge of reviewing and resolving any discrepancies. Familiarity with CMC T-Cell data is a plus. REQUIRED KNOWLEDGE, SKILLS AND ABILITIES Basic knowledge of applicable research and regulatory requirements, i.e., ICH GCP and relevant local laws, regulations and guidelines Exposure to MS Applications including but not limited to Microsoft Word, Excel and PowerPoint Effective written and verbal communication skills including above-average command of English language Effective time management skills Results and detail-oriented approach to work delivery and output Ability to establish and keep-up effective working relationships with coworkers, managers and clients Strong listening and phone skills Good data entry skills Qualification: Life Science Graduates Mandatory Skills: MS Excel, Good communication skills Schedule interview : If above Requirements matches to your profile can send your updated CV to : Vani.B@technosoftcorp.com and reach at 9182991774 (drop me a text message)* Note : Ignore, if JD not matches to your profile &amp Do Refer to your Friends &amp Colleagues Regards Vani B 9182991774 Vani.B@technosoftcorp.com

Job Description:Dear Candidate We are conducting a WalkIn&amp amp nbsp Recruitment Drive for Clinical SAS Programmer in Chennai on 19th May. Exp- 2.5 yrs-8 yrs Job Description Good Clinical Domain knowledge grasp clinical phases and Work exp must be in clinical domain with min 2 projects (Phase I-IV). Create Data transfer specification by referring the eCRF, Annotation of eCRF, knowledge on Protocol. Create SAS datasets of clinical data from raw data create status and efficacy datasets create project specific macros and formats load client data from other platforms prepare data to be sent to clients. Create listings and Custom reports as per customer requirement. Knowledge on Vendor Import programmer Strong Technical knowledge on SAS programming, CDISC SDTM standards, Semi SDTM (Sponsor based standards). SAS /BASE, SAS/Advance SAS, SAS/ Macros, SAS/SQL &amp amp amp SAS/SAS Grid knowledge is required. Data listings, in accordance with approved statistical analysis plan and shell displays for clinical research studies. Code is to be written using Base SAS programs, SAS procedures, or standardized macros. Perform data checks as needed to understand structure and content of data. Coordinate the different project stake holder on project deliverables. Create and keep-up Standard QC documentation and keep-up the accuracy. Good Communication skill &amp amp nbsp Job Location: Bangalore &amp amp nbsp Chennai Venue &amp amp nbsp IBIS City Center 690, Anna Salai, Mount Road, Near US Consulate, Thousand Lights, Chennai, Tamil Nadu 600006, India kindly send across your updated CV to Naveen.alexander @quintiles.com and walk down to our venue on 19th May. Note:- Clinical domain expertise only apply Thanks and regards Shruti Pandurang

Job Description:Hi Greetings from Technosoft Corporation !! About Technosoft: Technosoft is an integrated Information Technology (IT) and Business Process Management (BPM) solutions provider. Our collaborative culture and work environment helps attract and retain exceptional talent which is a key ingredient to address our clients needs, and help drive our sustained growth. Our biggest differentiators include: A Focused Service Portfolio Customer-Centric Approach Outcome-Based Model Exceptional Talent Culture of Curiosity and Confidence Technosoft has approximately 3,600+ employees worldwide. Our global footprint spans across North America, India, UK, Australia and New Zealand, and the Middle East. Our vision is to be partner and employer of choice in our chosen segment. For more information, visit us at www.technosoftcorp.com Specialties: IT Consulting, BPM services, Healthcare IT, Data Sciences, Mobility, Global In-house Centers, Professional Staffing. Immediate requirement for "Clinical Process Trainee" in Thane (Mumbai) Location. Contact : Harsha(8686007264) Forward Your Updated CV to : saimahesh.k@technosoftcorp.com Job Description : Experience 6 Months - 4 Years (Clinical Process Trainee) Notice Period: Immediate Should be flexible with Thane location Skills required - Good Communication Skills Verbal + Written / Excel Skill Roles &amp Responsibilities: Complete appropriate role-specific training to perform job duties Under supervision, perform assigned administrative tasks to support team members with project execution (examples of such tasks include but not limited to running system reports, keep-uping minutes of meeting, put-together and distributing status reports, creating and keep-uping study documents, etc.) Under supervision, assist in updating and keep-uping systems within project timelines and per project plans The staff will review the PDF file and locate the appropriate fields for entry into an excel database. Double-data entry will be used for this service. A comparison will be performed between the initial entry and the double data entry. The staff will be in charge of reviewing and resolving any discrepancies. Familiarity with CMC T-Cell data is a plus. REQUIRED KNOWLEDGE, SKILLS AND ABILITIES Basic knowledge of applicable research and regulatory requirements, i.e., ICH GCP and relevant local laws, regulations and guidelines Exposure to MS Applications including but not limited to Microsoft Word, Excel and PowerPoint Effective written and verbal communication skills including above-average command of English language Effective time management skills Results and detail-oriented approach to work delivery and output Ability to establish and keep-up effective working relationships with coworkers, managers and clients Strong listening and phone skills Good data entry skills Qualification: Life Science Graduates Mandatory Skills: MS Excel, Good communication skills Schedule interview : If above Requirements matches to your profile can send your updated CV to : saimahesh.k@technosoftcorp.com and reach at 8686007264 (drop me a text message)* Note : Ignore, if JD not matches to your profile &amp Do Refer to your Friends &amp Colleagues Regards Harsha 8686007264 saimahesh.k@technosoftcorp.com

Job Description:Training the subjects on dos and donts during study. Coordinate with investigator and coordinators for drug administration activity. Coordinate with the clinical staff for PK sampling. Monitoring the subjects during the study. Handling and reporting of adverse events to investigator / physician. Coordinate with the clinical staff for standardized diet distribution. Make sure that subject compliance to all the study related activities.

Job Description:I)Provides Qualifications and Agreements by: Maintaining current, up-to-date curriculum vitae. Maintaining current licmake sure that to practice. Demonstrating the proper education, training and experience to conduct the clinical investigation. Assuming duty for the conduct of the clinical investigation. II)Make sure thats Protocol Compliance by: Possessing a thorough grasp of the requirements of each protocol. Determining that inclusion / exclusion criteria are applicable to the study population. Ensuring recruitment goals are reasonable and attainable. Reviewing the inclusion / exclusion criteria, schedule of visits, end point criteria and investigational article use with the research team. III)Manages the Medical Care of Subjects by: Assessing subject compliance with the test product and follow-up visit. Assessing subjects response to therapy. Evaluation of adverse experiences. Ensuring that medical care is provided to a subject for any adverse event(s) that is reported. Informing a subject when medical care is needed to treat an inter-current illness(es). IV)Protects the Rights and Welfare of Subjects by: Ensuring that the informed consent form contains all the elements required. Obtaining a signed and dated informed consent from the subject or subjects legal representative prior to initiation of any study-related procedures. Informing the subject or legal representative about all aspects of the clinical trial. V)Make sure thats Documentation of Study-Related Procedures, Processes and Events by: Conduction of physician examination as per the protocol and applicable procedures for volunteers. Documenting deviations from the approved protocol. Documenting that informed consent has been obtained from the subject or legal representative. Documenting adverse event(s). Complying with written procedures to document changes to data and / or case report forms. Maintaining trial documents as required by the regulations and sponsor for the appropriate timeframe and under secure conditions. VI)Maintains Professional and Technical Knowledge by: Attending education workshops. Reviewing professional publications. Participating in professional societies.

Job Description:Jd' s: ~Having a working experience in study sample analysis, Method ~Method validation and method development in ADL dept. Review all analytical data and analytical study report preparation. ~Having working experience with LC-MS/MS, HPLC, GC.

Job Description:M. Pharm / M.Sc in chemistry Hands on experience in QA and handling QMS system and Risk analysis Exp. having worked in API / Formulation plant with regulatory approval from USFDA, MHRA, EDQM Shall have above-average knowledge and requirement QMS and ICH Q9.

Job Description:Patients' Medical Information into standard Diagnosis codes(ICD-10CM) and Procedure Codes(CPT). Requirements: Age should be below 30. Good Communication skill. Benefits- Weekends off/Cab/Food/Incentives Contact: HR Kausalya - 9952034365 Core2Code

Job Description:Perform experiments for development analytical methods such as Assay, Related Substances &amp amp Dissolution for oral solid dosage forms by HPLC. Carry out Stability Study, Forced Degradation Study &amp amp excipient compatibility study of formulations.

Job Description:Dear Candidate, Greetings From RESOLVE MEDICODE!! We are hiring Fresher - Medical Coder, Medical Coding is the process of converting Verbal Descriptions into numeric or alpha numeric by using ICD 10-CM, CPT &amp amp amp HCPCS. Medical Coders should review the documentation contain patients medical records and translate it into universally accepted industry-standard code. Pay Scale: 10,000 to 18,000 (Fresher) &amp amp amp upto 50,000(Experienced) per month with assured career growth (Incentives &amp amp amp Benefits as per Corporate Standards). Benefits - Weekends off Cab Food/Incentives Eligibility : Nursing, Pharmacy, Botany, Zoology, Microbiology, Biochemistry, Biotechnology, Plant Botany &amp amp amp Biotechnology, Advance Zoology &amp amp amp Biotechnology, Psychology, Nutrition &amp amp amp Dietetics, Diploma courses in Allied health Sciences etc., Requirements: Candidate should be from Medical/Paramedical Life Science Allied Health Sciences Strong knowledge in Anatomy, Physiology and Pathology. For Details Princia Recruitment Associate 8148052460 http://medi-code.in/

Job Description:Hi, Greetings from Technosoft Corporation !!! About Technosoft: Technosoft is an integrated Information Technology (IT) and Business Process Management (BPM) solutions provider. Our collaborative culture and work environment helps attract and retain exceptional talent which is a key ingredient to address our clients needs, and help drive our sustained growth. Our biggest differentiators include: A Focused Service Portfolio Customer-Centric Approach Outcome-Based Model Exceptional Talent Culture of Curiosity and Confidence Technosoft has approximately 3,600+ employees worldwide. Our global footprint spans across North America, India, UK, Australia and New Zealand, and the Middle East. Our vision is to be partner and employer of choice in our chosen segment. For more information, visit us at www.technosoftcorp.com Specialties: IT Consulting, BPM services, Healthcare IT, Data Sciences, Mobility, Global In-house Centers, Professional Staffing. Hiring for "Clinical Process Associate" in Technosoft, Bangalore. JD: Job Location: Bangalore Experience Range: 1 year - 2 Years* Skills required - CRA knowledge, CRC knowledge, Patient Data knowledge, ICH - GCP, ICF, Adverse Events/ SAEs, site monitoring, remote site monitoring knowledge. (eTMF - experience - not mandatory but preferred). PURPOSE: Provide project related assistance for assigned complex project(s), sites and project teams. Make sure that all work is conducted in accordance with SOPs, policies and practices, above-average clinical practices and applicable regulatory requirements and meets quality and timeline metrics. DUTIES : Perform complex processes and tasks that eventually result in high quality deliverables that are completed according to service level agreements (SLAs) and within project timelines Establish and keep-up effective project/ site communications Create and keep-up relevant project documents Make sure that accurate completion and upkeep of internal systems, databases, tracking tools, timelines and project plans with project specific information Participate in document management (creation, review, upkeep, storage, as applicable) REQUIRED KNOWLEDGE, SKILLS AND ABILITIES Good knowledge of applicable clinical research regulatory requirements i.e., ICH GCP and relevant local laws, regulations and guidelines Strong written and verbal communication skills including above-average command of English language Results and detail-oriented approach to work delivery and output Good problem solving skills Good planning, time management and prioritization skills Attention to detail and accuracy in work Good software and computer skills, including MS Office applications including but not limited to Microsoft Word, Excel and PowerPoint Ability to establish and keep-up effective working relationships with coworkers, managers and clients. Proven ability to work on multiple projects balancing competing priorities Ability to coach/ mentor junior colleagues Any clarifications please feel free to call me on the co-ordinates in my signature below / Email to : Bindusri.a@technosoftcorp.com Regards Bindu 7989626219 Bindusri.a@technosoftcorp.com

Job Description:Hi, Greetings from Technosoft Corporation !!! About Technosoft: Technosoft is an integrated Information Technology (IT) and Business Process Management (BPM) solutions provider. Our collaborative culture and work environment helps attract and retain exceptional talent which is a key ingredient to address our clients needs, and help drive our sustained growth. Our biggest differentiators include: A Focused Service Portfolio Customer-Centric Approach Outcome-Based Model Exceptional Talent Culture of Curiosity and Confidence Technosoft has approximately 3,600+ employees worldwide. Our global footprint spans across North America, India, UK, Australia and New Zealand, and the Middle East. Our vision is to be partner and employer of choice in our chosen segment. For more information, visit us at www.technosoftcorp.com Specialties: IT Consulting, BPM services, Healthcare IT, Data Sciences, Mobility, Global In-house Centers, Professional Staffing. Hiring for "Clinical Process Associate" in Technosoft, Bangalore. JD: Job Location: Bangalore Experience Range: 1 year - 2 Years* Skills required - CRA knowledge, CRC knowledge, Patient Data knowledge, ICH - GCP, ICF, Adverse Events/ SAEs, site monitoring, remote site monitoring knowledge. (eTMF - experience - not mandatory but preferred). PURPOSE: Provide project related assistance for assigned complex project(s), sites and project teams. Make sure that all work is conducted in accordance with SOPs, policies and practices, above-average clinical practices and applicable regulatory requirements and meets quality and timeline metrics. DUTIES : Perform complex processes and tasks that eventually result in high quality deliverables that are completed according to service level agreements (SLAs) and within project timelines Establish and keep-up effective project/ site communications Create and keep-up relevant project documents Make sure that accurate completion and upkeep of internal systems, databases, tracking tools, timelines and project plans with project specific information Participate in document management (creation, review, upkeep, storage, as applicable) REQUIRED KNOWLEDGE, SKILLS AND ABILITIES Good knowledge of applicable clinical research regulatory requirements i.e., ICH GCP and relevant local laws, regulations and guidelines Strong written and verbal communication skills including above-average command of English language Results and detail-oriented approach to work delivery and output Good problem solving skills Good planning, time management and prioritization skills Attention to detail and accuracy in work Good software and computer skills, including MS Office applications including but not limited to Microsoft Word, Excel and PowerPoint Ability to establish and keep-up effective working relationships with coworkers, managers and clients. Proven ability to work on multiple projects balancing competing priorities Ability to coach/ mentor junior colleagues Any clarifications please feel free to call me on the co-ordinates in my signature below / Email to : saimahesh.k@technosoftcorp.com Regards Harsha 8686007264 saimahesh.k@technosoftcorp.com

Job Description:Dear Candidate, Greetings From RESOLVE MEDICODE!! We are hiring Fresher - Medical Coder, Medical Coding is the process of converting Verbal Descriptions into numeric or alpha numeric by using ICD 10-CM, CPT &amp amp amp HCPCS. Medical Coders should review the documentation contain patients medical records and translate it into universally accepted industry-standard code. Pay Scale: 10,000 to 18,000 (Fresher) &amp amp amp upto 50,000(Experienced) per month with assured career growth (Incentives &amp amp amp Benefits as per Corporate Standards). Benefits - Weekends off Cab Food/Incentives Eligibility : Nursing, Pharmacy, Botany, Zoology, Microbiology, Biochemistry, Biotechnology, Plant Botany &amp amp amp Biotechnology, Advance Zoology &amp amp amp Biotechnology, Psychology, Nutrition &amp amp amp Dietetics, Diploma courses in Allied health Sciences etc., Requirements: Candidate should be from Medical/Paramedical Life Science Allied Health Sciences Strong knowledge in Anatomy, Physiology and Pathology. For Details Suchithra Recruitment Associate 7500052460 http://medi-code.in/

Job Description:No. NIRT/PROJ/NEW/RECTT/2018-19 Dt: 04.05.2018 No of Post: (UR-4, OBC-1) Essential qualification: MBBS degree from a recognized university Desirable: Any Postgraduate degree/Diploma (MD/MS/DNB/Diploma) in Medical Sciences. Previous experience in conduct of Randomised Clinical Trials Age limit: Not exceeding 35 years. Age relaxation as per GOI norms. OBC job-seekers will have to produce certificate as per GOI format. Emoluments: Consolidated salary Rs.60,000/- p.m. 6 Nature of Duties: Patient recruitment, enrolment, clinical management and monitoring of study participants Generating and submission of SAE forms and toxicity reports to IEC/sponsor and Overall in charge of co-ordination of study/research activities with the sponsors and carry out the study as per study protocol. Duration: Initially for a period of one year Venue: National Institute for Research in Tuberculosis, No.1, Mayor Sathyamoorthy Road, Chetpet, Chennai &amp amp ndash 600031 Date of Walk-in-Interview/Written Test Reporting time: 30/05/2018 (Wednesday) 9.00 AM TO 10.00 AM (interview from 11.00 AM onwards) For more details: http://www.icmr.nic.in/icmrnews/new%20project%20appointments%20-%20different%20projects%20-%20final-%20advt.pdf

Job Description:Medical reviewers examine medical documents for accuracy, such as looking at patient records and insurance paperwork. They can work in medical facilities or for independent firms. Call/watsapp- 9566120230

Job Description:Coordinate and document internal regulatory processes, such as internal audits, inspections, license renewals, or registrations. May compile and prepare materials for submission to regulatory agencies.

Job Description:Candidate post: Legal Officer Shivashakti Group of Companies Work place: Hyderabad (Corporate Office) Candidate Qualification: L.L.B Degree from recognized University. &amp amp nbsp Subject knowledge: Should have min. 1 year of practicing Experience in court of law. Subject knowledge of Consumer protection act, Cr.Pc, FOC, Insecticides Act, Civil Laws, Evidence Act, MV Act, Sec-138 Cases,Corporate Law &amp amp amp Labour Laws etc., &amp amp nbsp Communication, Conciliation &amp amp amp Drafting skills: Candidate should speak, read &amp amp amp right languages English &amp amp amp Hindi and should have above-average Communication Skills, Conciliation Skills &amp amp amp knowledge to draft all kinds of The Complaints, petitions, representations, Agreements, reply against the divisional issues or notices, reply notice, counter etc., Salary: in-between 15K - 18K P.M.

Job Description:Specification and acceptance testing of new equipment, as well as standard quality control of existing equipment. Radiation protection, to make sure that the safety of patients, staff and the public. Software, spreadsheet and database development. Equipment calibration and quality assurance.

Job Description:Qualification: MBA (HR) No of Position : 02 Internship period: 6 Months Location: Gagillapur Work Timings: 09:00 AM to 05:00 PM

Job Description:Dear Candidate, Greetings From RESOLVE MEDICODE!! We are hiring Fresher - Medical Coder, Medical Coding is the process of converting Verbal Descriptions into numeric or alpha numeric by using ICD 10-CM, CPT &amp amp amp HCPCS. Medical Coders should review the documentation contain patients medical records and translate it into universally accepted industry-standard code. Pay Scale: 10,000 to 18,000 (Fresher) &amp amp amp upto 50,000(Experienced) per month with assured career growth (Incentives &amp amp amp Benefits as per Corporate Standards). Benefits - Weekends off Cab Food/Incentives Eligibility : Nursing, Pharmacy, Botany, Zoology, Microbiology, Biochemistry, Biotechnology, Plant Botany &amp amp amp Biotechnology, Advance Zoology &amp amp amp Biotechnology, Psychology, Nutrition &amp amp amp Dietetics, Diploma courses in Allied health Sciences etc., Requirements: Candidate should be from Medical/Paramedical Life Science Allied Health Sciences Strong knowledge in Anatomy, Physiology and Pathology. For Details Princia - hr 8148052460 http://medi-code.in/

Job Description:Dear Candidate, We are having an urgent requirement for Clinical Data Management&amp amp nbsp for Bangalore &amp amp amp Mumbai work location. We are having a WalkIn Recruitment Event on 19th May 2018 at Bangalore &amp amp amp Chennai Location. Bangalore Venue :: Prestige Technology Park II,&amp amp nbsp Etamin Block B Wing 1st Floor , Sarjapur-Marathahalli , Outer Ring Road , Bangalore 560 103 India Reporting Time : 8:30 AM Bangalore Contact Person :: Shruti.Pandurang &amp amp amp Sajitha Chennai Venue :: Will Be shared shortly &amp amp nbsp Chennai Contact Person :: Naveen Alexander Reporting Time : 8:30 AM Do review the below mentioned Job Description and if it matched with your career aspiration do share your CV to Shruti.Pandurang@quintiles.com&amp amp nbsp Note : Candidate should have 2 - 7 years of experience in RCLinical Data Management for Study Bulid/eCRF bulid,Edit Checks,UAT ,Data Validation. Candidates who have attended interview with IQVIA in the past 6 months will not considered.(Technical Face to Face /Skype Video Interview). Documents to bring : Pan Card (Photocopy), Aadhar Card (Photocopy) and Updated Resume. Job Description :: VTL EDTS/SAS Primary Responsibilities Test plan author : Creates the respective test plan. a. Should possess the skill to read and understand the following documents Protocol (latest approved version) SAS Listing Specifications (latest approved version) Edits specification (Latest approved version) Data Transfer Specifications (specifically referring to SAS labels and formats associated with checks if available) Non-CRF Data Guideline and Vendor data test files (applicable only if Vendor data listings are included in SAS Listing Specifications) Latest version of Architect Loader Spreadsheet (ALS), Annotated Study Book (ASB), or Time and Events, as applicable. b. &amp amp nbsp Might be required to enters test data within the EDC system/CDMS to test the Edit Checks or SAS Listings according to the Test Plan. c. Might be required to Enter Test Data outside the EDC System/CDMS (SAS listings only, e.g., non-CRF data