63 Bio-Tech, Clinical Research jobs

Dear Candidate, Greetings from CHC Health Care Pvt Ltd.!!!! We are inviting freshers to start their careers with us; please refer to the JD below:  Interpret & Analyse cardiac ECGs.   Skill Set- Good Computer Usage Skills. Good English Written Skills. Ability to Work in different shifts( For Boys) For Girls only Day Shifts. Willing to build a long term career in healthcare.   Industry - Medical/ Healthcare Functional Area- Freshers   Specialization- Sc( Physics/Chemistry/Botany/Zoology/Maths Pharmacy/ Biotechnology/ Microbiology. BA(Prog)   Any Graduate/Post Graduate Only Freshers  Interested candidate can share there resumes at hr@chcgroup.in or can directly come for interview at Address Detail:  Corporate office- 26/1, East Patel Nagar , New Delhi - 110 008, India .   Nearest Metro Station is - Patel Nagar( Blue Line) Nearest Landmark is - Pooja Park & Axis Bank   Regards, Pratibha Sharma 9999120289

Interpret & Analyse cardiac ECGs.   Skill Set- Good Computer Usage Skills. Good English Written Skills. Ability to Work in different shifts( For Boys) For Girls only Day Shifts. Willing to build a long term career in healthcare.   Industry - Medical/ Healthcare Functional Area- Freshers Specialization- Sc( Physics/Chemistry/Botany/Zoology/Maths Pharmacy/ Biotechnology/ Microbiology. BA(Prog) ANY GRADUATE/POST GRADUATE ONLY FRESHERS Regards, Pratibha Sharma 9999120289 26/1 East Patel Nagar(Patel Nagar Metro Station- Blue Line)

Duties and Responsibilities: The key responsibility of the Assistant Clinical Educator in consultation with the Educator is to meet the educational needs of the clinical staffs in the organisation. Specific responsibilities of the Clinical Educator include but are not limited to: Education & Training: Orientation of new employees to the job profile Development and management of Mandatory education Clinical support and ongoing education of employees Assessment of employees using clinical competencies. Identify and respond to the learning needs of individuals and the service Management in the planning, implementation, and delivery of educational curricula Initiates skills development programs within the parameters of established; monitors trends and implements educational strategies to ensure compliance with quality standards and parameters Educates technical staff in the use of new services; co-ordinates in-service training and workshops for appropriate staff Provides educational leadership to all clinical employees to enhance specialized clinical knowledge within established clinical protocols Evaluation of the effectiveness of education within the organisation Demonstrate a high level of understanding, knowledge and skills in Clinical training, Team management, Quality control and re-education Attend staff meetings, job fairs, and other organization sponsored meetings and activities. Maintain updated information concerning new advances and procedures in your field through continuing education Will consult with employees, via agreed mechanisms, to enable employees to contribute to the making of decisions affecting health, welfare and safety at work Ensure provision of appropriate clinical training for all employees to enable them to carry out their work efficiently Comply with all relevant organizational Code of Conducts and rule & regulation always Supervise employees to ensure adherence of approved policies and procedures Prepare exams and maintain an accurate electronic grade book Monitor student grades/attendance and input on a daily basis Hands-on training when available Effective communication & interpersonal skills with problem solving ability The ability to relocate to other sites within India may at times be required Record Keeping Responsibilities: This applies electronic record-keeping environment. Keeping the record of all official activities is the responsibility of all staff members. Staff should ensure that records are created, captured into authorised record keeping systems, maintained, protected from unauthorised use, retained and disposed of in line with CHC policy on corporate records management Privacy Responsibilities: It is the responsibility of all staff to ensure privacy of personal information by following HIPPA (Health Insurance Portability & Accountability Act) privacy and security procedures in relation to any personal health information accessed during the course of their duties Duties as assigned Quality Improvement and Management Undertake the necessary components of the performance review process Promote and participate in quality improvement activities and organisational accreditation processes Participate in relevant committees, meetings and service activities as required and provide relevant feedback and dissemination of appropriate information Assess and evaluate the quality of education resources required to meet the learning needs of employees in the retrieval environment Actively pursue opportunities to advance own professional knowledge and skill development Act as an effective role model for staff, through mentoring, and teaching in an endeavour to achieve optimal staff development and service outcomes Knowledge, Skills and Abilities Required Thorough knowledge and understanding of clinical protocol, procedures, and standards within area of nursing expertise Ability to provide operational guidance and leadership to technical staff in area of specialty. Knowledge of related accreditation and certification requirements Ability to assess educational needs and design and develop responsible curricula Working knowledge of the use of established clinical and preceptorship models in the development of clinical education programs Technical leadership skills within area of expertise Ability to plan, implement, and evaluate individual educational and training programs Highly developed verbal and written communication skills and the ability to present effectively to small and large groups Strong interpersonal skills and ability to work effectively at all levels in a collaborative team environment Regards, Pratibha Sharma 9999120289

Interpret & Analyse cardiac ECGs.   Skill Set- Good Computer Usage Skills. Good English Written Skills. Ability to Work in different shifts( For Boys) For Girls only Day Shifts. Willing to build a long term career in healthcare.   Industry - Medical/ Healthcare Functional Area- Freshers    Specialization- Sc( Physics/Chemistry/Botany/Zoology/Maths Pharmacy/ Biotechnology/ Microbiology. BA(Prog)  Only Freshers are required. Interested candidates can share there resumes at [email protected]  or can call at 9999120289 Direct face to face interviews are going on at below mentioned address: Corporate office- 26/1, East Patel Nagar , New Delhi - 110 008, India .   Nearest Metro Station is - Patel Nagar( Blue Line) Nearest Landmark is - Pooja Park & Axis Bank  Timing: 10:00 AM to 5:00 PM Regards, Pratibha Sharma 9999120289

*Should have exp of 2-5 yrs * Overall responsibility for conducting Mutagenicity studies * Responsible for the preparation of study plan, study report. * Distribution of study plan to management and Quality Assurance. * In charge for Genotoxicology department.

Associate Editors-Biomedical Sciences (Office or Telecommute)   Cactus Communications is a leading provider of scientific communication services to more than 60,000 clients across 116 countries. We are currently looking to hire Associate Editors in the Biomedical Sciences field. This is a full time position which could either entail working from office in Mumbai or working from home (telecommute).   WHAT YOU WILL DO: ·         As an associate editor, you will help researchers improve the language and clarity of their documents and ensure that the documents comply with style and format requirements. ·         Manage deadlines and have high quality standards. ·         Review the assignments done by editors and provide timely feedback with the aim of making them independent contributors.   WHY THIS IS A GREAT OPPORTUNITY: ·         This position permits flexibility. Candidates from any part of India are invited to apply. You can choose to either telecommute or work from our office in Mumbai. ·         You will receive training to become adept at editing and reviewing both academic and non-academic manuscripts and will be provided with the necessary technological support (laptops will be provided to telecommuters). ·         You will also have unlimited access to exclusive interviews with industry experts, articles on the latest industry trends, and publication and writing tips on our learning and discussion platform. ·         At CACTUS, you will be exposed to research carried out worldwide and will get an insider’s view of the burgeoning, multi-million-dollar publishing industry.   WHAT YOU NEED: ·         A degree (bachelor’s, master’s, PhD, etc.) in the biomedical sciences field (detailed subject-area list below) ·         Excellent written English skills and attention to detail ·         Familiarity with MS Word, Excel, and PowerPoint   APPLICATION PROCESS To apply, please access this link: http://bit.ly/1Wlaojl DETAILED SUBJECT- AREA LIST: Biochemistry, Genetics and Molecular Biology, Neuroscience, Ecology, Medicine, Pharmaceutical Sciences etc.

Responsibilities/Authorities 1. Create and/or annotate and review tables and listings mocks; ensure internal consistency within and among tables and listings; ensure that all CRF fields are displayed on listings. 2. Review clinical data for outliers, invalid and illogical data points. 3. Interact with Clinical Data Management (CDM) to resolve data issues. 4. Must be able to use Univariate’s, frequencies, Proc Transpose, and macros, including modifying existing macros and writing macros. 5. Follow all pertinent SOP’s and guidelines concerning programming and the change control management of all files generated by the Biometrics Programming group. 6. Program routine data displays, such as 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. 7. Write and compare independent QC programs to verify the output generated for data displays. 8. Coordinate QC project teams on large projects, which includes training and delegation of QC work. 9. Create and maintain standard QC documentation. 10. Maintain tables and listings binders, if applicable, which include a hard copy of the latest versions sent to the client. 11. Send tables and listings to clinical writers and clients, which include printing, collating, and filling out appropriate shipping paperwork. 12. Attend both client and team meetings when needed. 13. Respond to non-statistical questions from Clinical Writing and from clients. ? Assist in establishing departmental processes, interaction with other departments, training of staff, and other departmental administrative tasks.   Requirements: ? Experience on PC platform. ? Proficient in at least one computer language, i.e., i.e., SAS, Oracle database programming, C  Required Qualification: ? Proficient in at least one computer language, i.e., i.e., SAS, Oracle database programming, C++, FORTRAN.

We are providing Advanced PG Diploma in Clinical Research, Pharmacovigilance, Regulatory and Clinical Data Management ( SAS Clinical, Oracle Clinical Programming and Pharmacovigilance Software )Training with internship and Job Placement. If you are interested to pursue your career in Clinical Research and Clinical Data Management please Call and Visit us at Avesthagen Ltd, Discoverer 9th Floor, ITPL, Whitefield Road, Bangalore-66. Contact : Dr.Shaw Mobile  : 09886735658   Web Site : http://www.avclinicaltraining.com        www.avesthagen.com

Biovigor Lifescience Pvt Ltd is a leading biotech company in India. We are exclusively representing some of leading diagnostic companies from Europe and US. We are major player in Elisa,CLIA and Rapid. We are looking for young, dynamic and committed professionals to work as part of our team in our organization.  Designation: Sales Executive(Experience:0-2 Years in the sales admin activities,Elisa marketing experience would be a plus).  Job Location: Hyderabad  Main Duties and Responsibilities:  The person would be in charge of sales and marketing of various Elisa diagnostic products.  Visiting Diagnostic centers,Corporate Hospitals and visiting doctors to promote products.  Visiting major distributors,retailers,sub dealers.  To prepare quotations and Tenders of Govt as well as Private Institutions. Qualification-Graduate in any Science discipline.  Desired job-seeker should be fluent in English, hardworking and dynamic personality  Having command over MS-office and other basic computer applications with good communication skills(Written as well verbal).  Loyalty to the company is a must.  Able to meet the challenges in the field act independently.

Trainer-Medical coding, ICD-10, CPT, PCS

To prepare protocol specification for quotes including appropriate design of the study, review of study protocols and reports To perform pre-study screening, assessment of eligibility criteria, medical care, ADR and AE monitoring and emergency management of ADRs and SAEs. Training Clinical Research Staff for recent trends and advance Preparation & review of key Clinical Research documents Preparing and supervising the preparation of laboratory reports and scientific papers Overall responsible for organization and conduct of bioequivalence and pharmacokinetic studies in conformance to GCP standards, SOPs, and applicable regulations To ensure that all professional and technical personnel involved in the conduct of the study have job descriptions and records of training, qualification and experience, which support their ability to undertake the tasks assigned to them Review medical records and ascertain eligibility of subjects To review the protocols, informed consent documents and CRFs for all clinical studies To prepare project plan in co-ordination with designated personnel To ensure the conduct trials with compliance to SOPs and GCP/GLP requirements To facilitate monitoring and auditing by the sponsor and inspections by any regulatory authorities. To liase with Ethics Committee for review of study protocols and informed consent documents To supervise the activities of clinical staff To ensure proper reporting of adverse events to sponsor / Ethics Committee/ regulatory authorities To ensure reporting of SOP/ protocol deviations in accordance with SOPs To ensure proper volunteer compensation To obtain written informed consent from study subjects To carry out medical examination of volunteers for screening prior to clinical studies or as required To manage medical emergencies To ensure the accountability for study drug samples according to GCP guidelines and applicable GMP requirements To review the final study report of completed studies Impart GCP and other technical training (including protocol training) to study personnel To review SOPs and give inputs, as applicable during SOP development / revisions To maintain awareness in recent trends and newer guidelines in clinical research Response to provid Quality Assurance Unit queries

    Response to provid Quality Assurance Unit queries    

1. Analysing of ECG signals

1. Analysing and Interpretations of ECG 2. Training will be provided

A MNC specialized in Technologies for Lifescience support is looking for a marketing Communications specilaist.  If interested, please forward your CV to abirab@cdrivecareers.com

Qualified Nursing staff assisting Eye Surgeon in Operation theater Minimum 3 -5 years experience

 Supports US Research Medical Directors and/or US Client Medical Directors and Client Policy Managers to provide oversight for     the accuracy and quality of research materials originated from Medical Policy and Client Services  • Supports the scheduled review process for global and specialty policies in collaboration with the US Research Medical Directors  • Supports the scheduled review process for State Medicaid policies in collaboration with the US Client Medical Directors and/or Client Policy Managers  • Coordinates with US Research Medical Directors to manage the integrity of the Payment Policy Library and ensure the Payment Policy Library is accurate and up-to-date  • Supports quarterly and annual updates in collaboration with the US Research Medical Directors  • Ensures changes to rule sets are accurate, complete and are finished in a timely manner including documentation of notable changes  • Responds to the research related queries pertaining to the medical policy raised by internal personnel or client including but not limited to:  • Questions about claims edits that enforce medical policy  • Interpretation of how claims edits relate to policy statements.  • Recommendations regarding modifications of edits  • Conducts research to explore potential opportunities to expand the current medical policy set  • Partners well with global research team members to advance the Research agenda.  • Educates US Client Service MDs and Client Policy Managers (CPMs) on new changes and policy updates by actively participating in monthly meetings. 

We are providing Advanced PG Diploma in Clinical Research, Pharmacovigilance, Regulatory and Clinical Data Management ( SAS Clinical, Oracle Clinical Programming and Pharmacovigilance Software )Training with internship and Job Placement. If you are interested to pursue your career in Clinical Research and Clinical Data Management please Call and Visit us at Avesthagen Ltd, Discoverer 9th Floor, ITPL, Whitefield Road, Bangalore-66. Contact : Dr.Shaw Mobile  : 09886735658   Web Site : http://www.avclinicaltraining.com        www.avesthagen.com

1 – 2 years’ experience in extracting clinical studies, clinical trial review and analysis (efficacy and safety end points) is a must.         The ideal candidate should have excellent academic record with 2-3years of experience within Market research/Scientific literature review.

  VACANCY EPIDEMIOLOGIST for HIV/TB & MDR-TB Location of Job:   Manipur Last application date : 23rd November, 2012 Email: india-hrmco@oca.msf.org Availability: 1-2 years Salary indication: INR 46,777 Gross Monthly Salary Objectives of the position:  Defines, implements and follows up operational research activities in project area; ensuring the proper implementation of protocols, the development of proper methodology and the quality of the researches.   Main Tasks & Responsibilities  Plans and organises in close collaboration with other medical team members all epidemiological related activities performed in the project.   Participates in the definition and update of annual project planning and budgets. ·Supervises epidemiological research and ensures that protocols are adhered by all epidemiological staff. Ensures that contacts with various community groups and authorities are established and maintained according to the objectives of the researches. Ensures that a proper study of local context and population is done before starting any research or investigation. Ensures that patients or population participating in research are well informed and explained about reasons for doing research and do agree on their participation. Prepares protocol research and methodology according to guidelines (sample size, areas, groups to research, etc.) Set up inclusions procedures and data collection procedures.  Participates in selection and follow up of all epidemiology related staff in cooperation with the administration manager and field coordinator.   Organises and implements trainings of epidemiology related staff (implementation of procedures) Ensure that laboratory samples that come as a result of research are handled and transported to security rules and conditions needed for the sample. Ensures in coordination with logistics department that laboratory samples that need to be shipped nationally or internationally are done on time and following protocols. Informs other medical managers or doctors about any possible serious problem or complication, ex. witnessing of serious medical problems during research, etc. Participates in the monthly reports according to guidelines /SitReps, medical statistical reports, etc.)   Key requirements                                                Degree/Masters in Epidemiology or Public Health with extensive training in statistics and epidemiology Minimum 4 years experience in epidemiology and/or public health and in developing and implementing communicable disease control activities Ability to design and implement surveillance and other data collection systems for monitoring the medical programs Proven practical skills with software for statistical analysis and epidemiological database (Epi-info, SPSS, STATA, MSF Fuchia)  Ability to organize and prioritize workload & taking initiative when appropriate Good understanding of MS Office especially Word, Excel & PowerPoint Able to integrate into a multi-cultural team and cooperate with co-workers Demonstrates flexibility in taking up tasks outside of regular job responsibilities as required    Follow the linkfor full Job description http://www.msfindia.in/content.php?con_id=18 APPLY & MORE INFORMATION Please clearly state which position you are applying for and send your CV and cover letter to:                                           india-hrmco@oca.msf.org   Remarks : ·         Only short-listed candidates will be contacted. ·         Closing date for application : 23rd November, 2012

We are currently hiring for  Associate / Senior Associate (AR Calling)  position for our Hyderabad office. Please find the job responsibilities below.   Responsibilities: ·         Must have been in AR calling for at least 6 months - 3 yrs. ·         Responsible for calling Insurance companies (in US) and follow up on outstanding Accounts Receivable. ·         Good knowledge in Healthcare concept and Denial management. ·         Understand the client requirements and specifications of the project ·         Ensure that the deliverable to the client adhere to the quality standards. ·         Knowledge on various report generation ·         Preferably having knowledge of Doctor Calling and Patient Calling ·         Decent US accent with good communication skills. ·         Must be spontaneous and have high energy level. ·         Willing to Work for Night Shifts.   If interested, please reply back with your updated resume. Regards, HR

We are hiring fresher’s for US Medical Billing process (AR Calling - Voice) for our Healthcare Services Division. Role:  Process Associate Trainee Qualification: ·         Any Graduate (Except B. Tech & B.Pharmacy) 2011/2012/2013/2014/2015 Pass outs  ·         The Candidate should have good communication and analytical skills ·         The candidate should have good attitude. ·         Ready to give commitment of minimum 2 and half years. ·         6 months training is provided. ·         Ready to work in Night Shifts   Note:  Candidates who are pursuing final year or having backlogs are not eligible. Interested candidates can walk-in for written test and Interviews. Regards, HR http://www.elicohealthcare.com/

Jakob& Partners India Pvt. Limited is currently seeking Language Expert with 0-2 years of experience for the office located in Gurgaon. The Person should have good knowledge (written, spoken, and reading) of Russian language.     Jakob & Partners India Pvt. Limited established in year 2008 is seeking a core of young, dedicated and ambitious candidate who can contribute positively to expand the organization further in Asia Pacific market as well as contribute significantly to the overall growth of the company both in terms of projects as well as business segments. Language Expert will be responsible for direct communication and discussion with personnel In Russianpharmaceutical markets. The key Responsibility of language Expert will also include secondary research involving language translation Russian) to English and will respond to internal or external inquiries. The company may provide International training and work exposure depending on performance of the employee.     

Desired Candidate Profile   experience in.. *model validation & generation of reports. *automation of complex sas logic/programs. *very strong programming skills in sas and SQL. *ability to learn analytics and predictive modelling. *able to work in shifts.   Job Description excellent exp in SAS programming,proactively manage & deliver all assigned projects in core sas programming. provide technical guidance,background in analytics,implementation & scoring of marketing models in campaign.   Company Name:Chianalyst Consulting Website:www.chianalyst.com Email Address: career@chianalyst.com job ID:sas202

Wanted: Full-time Senior Editor for New Academic Editing Company in Mumbai   Job Description:   Edit research papers from non-native speakers of English for clarity, consistency and style.   Qualifications required :   Native or near native ability in English   Computer literacy with a good understanding of MS Word   Positive attitude, energetic approach and self-motivation are all essential   A critical eye for detail   Any of the below qualifications are preferred but not required:   Knowledge of academic writing conventions and the ability to edit and comment on non-native author’s research   Familiarity with academic writing style guides   Familiarity with non-native writing errors and their corrections   The ability to edit 8,000-10,000 English words per day if not doing any other tasks   Contact: hr@editingindia.com   Please put "Editor Position" in the subject line of the email. We thank all for their interest, but only the most qualified candidates will be contacted with a sample to edit. After surveying the sample we will contact qualified candidates for an interview.  

Wanted: Full-time Managerial Editor for New Academic Editing Company in Mumbai   Job Description:   Edit research papers from non-native speakers of English for clarity, consistency and style.   Qualifications required :   Native or near native ability in English   Computer literacy with a good understanding of MS Word   Positive attitude, energetic approach and self-motivation are all essential   A critical eye for detail   Any of the below qualifications are preferred but not required:   Knowledge of academic writing conventions and the ability to edit and comment on non-native author’s research   Familiarity with academic writing style guides   Familiarity with non-native writing errors and their corrections   The ability to edit 8,000-10,000 English words per day if not doing any other tasks   Contact: hr@editingindia.com   Please put "Editor Position" in the subject line of the email. We thank all for their interest, but only the most qualified candidates will be contacted with a sample to edit. After surveying the sample we will contact qualified candidates for an interview.

Zimedcode offers you the best in medical coding job.We train people into professionals with a comprehensive curriculum of international standard. Zimedcode offers you a Medical Coding Certification Program.  These certified programs are recognized internationally and the certified coders are in great demand.   Medical billing and coding training available of international standards at  Zimedcode!  We certainly need your service in medical billing and coding. We have plenty of vacancies for medical coding . Your job will be all about making simple conversions of treatment procedures done on patients into codes that can be used in medical insurance claim procedures.

Role: Medical Content Writer We are looking for Medical Content Writers to guide our 3D animation team for e-learning projects for medical students. Job Description Position is for medical content writer. An MBBS degree with good percentage. Preference will be given to candidates who have completed MD or BAMS in Anatomy or M.Sc. in Physiology, Biotechnology and Biochemistry. Experience in teaching will be preferred for senior medical content writers. Freshers are welcome for junior medical content writers. Work will be at office located at Nagarabhavi, Bangalore.  

Freshers: Candidates from life science background ( BSc, BTech, BParm, BPT, BDS, Biotech, Biochem, Nursing, Microbiology, Biomedical, Bioinformatics, Nutrition and Dietics, BAMS, BSMS, BHMS etc) Training can be arranged.

  Gain Through understanding of the products, prepare specification sheets and provide technical information to sales coordination team as and when required • Learn Application and prepare documents for reference.  Bring in Information of new products and find the applicability in the market • Provide Application support to the end users under Senior Application Specialist’s Supervision.  Understand the applications and prepare protocols, application notes, catalogues etc for the end users.  Attend to end users problem as and when directed by the supervisor.  Perform other assignments entrusted by supervisor from time to time.    DEPARTMENTAL GOAL    Business Development and Creating new Opportunities   Providing application support to the customers-who use our system/ instrument-in their respective fields, thus assuring orders for reagents kits and consumables. 

Looking Sales in Dehli & Baddi   2 Persons are required   Educational Qualification M.Sc - In Biosciences or Any Branch Of Science OR MBA with Science Background Upto Graduation or 10+2

POSITION: SCIENTIST / LEAD SCIENTIST EXPERIENCE : 0- 10 IN RESEARCH LOCATION: BANGALORE EDUCATION: MS / PHD – Computer Science or Biomedical or Electrical or Instrumentation PREF EXPERIENCE /SKILLS: BIO MEDICAL SIGNAL PROCESSING & PATTERN RECOGNITION OR MACHINE LEARNING , Data Mining or Cloud Computing ,ARTIFICIAL INTELLIGENCE Language: C/C++ Or Java ,J2ee NOTE: ONLY INDIAN CITIZITEN CAN APPLY FOR THIS JOB & PEOPLE ANYWHERE IN GLOBE CAN APPLY FOR THIS JOB for further details or queries pls contact aprraj@hotmail.com thanks Prithiviraj Mobile:99869 46638  

Require MBBS fresher, preferably who is well conversant with Kannada, for a role of PI for a leading CRO in Bangalore, Salary no constrain for a right candidate.

Strand life sciences, India, Bangalore is looking for a qualified genetic counsellor with at least a couple of year of experience in genetic counselling of patients and talking to Physicians. We will train you in next generation sequencing diagnostics. Attractive salary based on experience. If you are interested kindly send in your resume. We are looking for NRI and highly experienced and qualified  personnel in the field of genetics

  Strand is launching a one year online-plus-contact training program split into 32 online modules spread over 8 months with practical observation and participation in counselling sessions, lab operations and bioinformatics application to NGS diagnosis.  The weekly study would be 8-12 hours on a minimum. At the end of the training you will have to take an exam and top two graduates who get a grade >65% will be offered a job with probation of 6 months with handsome salary. As a part of contact training module, candidates need to occasionally visit Strand headquarters and laboratory at Bangalore. Applicants should be a minimum of MBBS with good credentials and computer skills. Apply immediately for the 2013 training in genetic counselling.

We are providing Advanced PG Diploma in Clinical Research, Pharmacovigilance, Regulatory and Clinical Data Management ( SAS Clinical, Oracle Clinical Programming and Pharmacovigilance Software )Training with internship and Job Placement. If you are interested to pursue your career in Clinical Research and Clinical Data Management please Call and Visit us at Avesthagen Ltd, Discoverer 9th Floor, ITPL, Whitefield Road, Bangalore-66. Contact : Dr.Shaw Mobile  : 09886735658   Web Site : http://www.avclinicaltraining.com        www.avesthagen.com

We are providing Advanced PG Diploma in Clinical Research, Pharmacovigilance, Regulatory and Clinical Data Management ( SAS Clinical, Oracle Clinical Programming and Pharmacovigilance Software )Training with internship and Job Placement. If you are interested to pursue your career in Clinical Research and Clinical Data Management please Call and Visit us at Avesthagen Ltd, Discoverer 9th Floor, ITPL, Whitefield Road, Bangalore-66. Contact : Dr.Shaw Mobile  : 09886735658 Web Site : http://www.avclinicaltraining.com

Individual Case Safety Report Processing. Fresher Life sciences and Pharamedical Sciences Graduates and Post Graduates willing to pursue career in Clinical Research and Clinical Data Management.

Biotech related jobs or Clinical research related.

  Clinical Data Manager   Clinical Data Coordinator   Clinical Data entry    e-CRF Designer/Study Builder   Clinical Project Manager   CRF Annotation   Data validation (edit/checks)   SAS-programmer  

ü  Candidate should posses excellent Communication Skills with pleasing personality. ü  Candidates having prior experience will be preferred, though a fresh graduate can also appear for Interview. ü  Completing supporting tasks assigned by the management within the provided time. ü  Custodian Duties. ü  Manage & monitor approximately 6 to 8 sites in multicentre  clinical  trial. ü  Ensuring site level compliance & adherence to regulatory requirement protocol & SOPs. ü  Coordinating with external vendors & internal team members for the smooth execution of the study ü  Maintaining study level & site level regulatory & study documents ü  Acting as a main point of contact between investigator & CRO to manage site level activities. ü  Conduct Site selection / Lab selection for investigational site and laboratories. ü  Participate and / conduct site meetings and multicenter investigator meetings and prepare reports. ü  Setting up the study centers, by ensuring each centre has proper training of all participants, adequate materials and ensure that the investigator knows exactly what has to be done. ü  Collate documents for Ethics committee submissions. ü  Review on-site files and records, case report forms and source documents for completeness, accuracy, consistency and compliance, identifies deficiencies and discrepancies and provides remedial training and / or initiates corrective action as required. ü  Verify that the investigator provides all the required reports, notifications, applications and submissions are timely, accurate, legible and complete and dated. ü  Assemble necessary documents; conduct site closure / termination visits to include investigational product reconciliation and disposition, review for completeness and accuracy of files, retrieval of relevant codes and documents. Assess suitability of archival facility and prepare study termination reports.

Define and direct the data management workflow for assigned projects in collaboration with statistician ensuring all necessary data quality control and integrity measures are in place Create, review, approve and maintain edit specification, CRF design, CRF Completion Guidelines, data cleaning procedures and other data management supportive tools with study team members according to protocol specific requirements and available guidance documents Review, analyze, and validate clinical trial data throughout the study lifecycle to ensure data consistency,completeness, integrity and accuracy based on project specific guidelines Query data inconsistencies and revise CRFs when necessary to comply with company and/or regulatory guidance and standard operating procedures.  Qualifications: Bachelor’s Degree and/or equivalent experience in Data Management.

The Drug Safety Associate is responsible for overseeing and performing specific tasks related to serious adverse event processing and reporting for assigned investigational product.  Ensures consistency in the initial evaluation and assessment of serious adverse event reports and source documentation for completeness, accuracy and legibility.  Exercises judgment and use of knowledge of FDA and ICH guidelines and product labeling in performing initial case assessment for seriousness, expectedness and listedness.  Job Requirements: Bachelor's degree in pharmacy or health-care related field required. Minimum of one year of pharmaceutical experience. Certificates, Licenses, Registrations an added advantage.

Under minimal supervision, coordinates the research and administrative activities of clinical trials for the practice by managing Regulatory and Quality Assurance procedures. Responsible for regulatory and safety support services including trial communication and document distribution, critical document collection process, safety reporting, translation of informed consent documents and communication with sponsor representatives. Provides this support in compliance with the FDA (CFR), ICH-GCP and DHHS guidelines. Qualifications: Requires a bachelor's degree in a related healthcare field. Job Training requirements: Regulatory certification or Internal operating procedures related to compliance is an added advantage. Candidates without the certification would be trained in the initial few weeks.

The SAS Programmer/Analyst will develop statistical analysis using standard reporting, ad hoc reporting, and data mining tools in order to identify patterns and trends.  Experience working with SAS Macro, format Libraries. Programming Knowledge in Data cleaning/Data export programs. Proven ability in Data Analysis. Supporting the Senior SAS programmer in the generation of tables, figure and listings using internal TFL SAS macro reporting system. Provide statistical programming support for multiple clinical research projects Produce datasets, analyses, tabulations, graphics and listings of clinical trials data. Contribute to on-going quality improvement efforts within the project. Good understanding of Medical/Clinical terminologies. Qualifications: 6+ months of experience in SAS programming,validation documentation, CDISC, SQL and Relational Databases.