- Novo Nordisk Inc. (Plainsboro, NJ)
- …interactions and developing and implementing regulatory strategies with the FDA to providing medical education and collecting data to support efficacy and new ... and effective use of products by patients and the medical community Determine appropriateness of data and...and the medical community Determine appropriateness of data and references used to support promotional claims and… more
- Insmed Incorporated (San Diego, CA)
- …all issues identified which may affect the quality and integrity of clinical studies. Medical monitoring, coding, and data cleaning in collaboration with Clinical ... the medical integrity of clinical study reports and data interpretation/communication.Author or oversee authorship of clinical sections of regulatory submissions… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …interactions and developing and implementing regulatory strategies with the FDA to providing medical education and collecting data to support efficacy and new ... and gain feedback from advisors Support other advisory boards with clinical data and other medical presentations Partner with professional associations and… more
- CHRISTUS Health (Tyler, TX)
- …Assisting the physicians, nurse practitioners, and physician assistants in giving superior medical care. Accurate Data Entry of charges on patient accounts, ... Description Summary: The Certified Medical Assistant will perform various services and related...related activities in support of patient care including accurate data entry for patient registration and insurance verification. The… more
- Novo Nordisk Inc. (Milwaukee, WI)
- …interactions and developing and implementing regulatory strategies with the FDA to providing medical education and collecting data to support efficacy and new ... About the Department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk...ensures and maintains awareness of current issues and new data pertaining to NNI products; b) develops and maintains… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …interactions and developing and implementing regulatory strategies with the FDA to providing medical education and collecting data to support efficacy and new ... About the Department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk...the Program. Extraction and interpretation of insights from scientific data , clinical experts or key external stakeholders. Opinion leader… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …interactions and developing and implementing regulatory strategies with the FDA to providing medical education and collecting data to support efficacy and new ... About the Department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk...you ready to make a difference? The Position Use medical and clinical expertise in design, implementation and monitoring… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- … Medical Monitor (MM):Provides oversight to the CRO MM for clinical data review activitiesMay support addressing eligibility and medical questions from sites/ ... with Clinical Scientists (CS)Interpretation and presentation of clinical study(ies) data to internal and external stakeholdersProvides medical /scientific… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …MM for clinical data review activities- May support addressing eligibility and medical questions from sites/ IRBs- May provide medical guidance for coding of ... with Clinical Scientists (CS)- Interpretation and presentation of clinical study(ies) data to internal and external stakeholders- Provides medical /scientific… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- … Medical Monitor (MM):Provides oversight to the CRO MM for clinical data review activitiesMay support addressing eligibility and medical questions from sites/ ... with Clinical Scientists (CS)Interpretation and presentation of clinical study(ies) data to internal and external stakeholdersProvides medical /scientific… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …of the company to quickly uncover new business opportunities through product data , input from external healthcare professionals, medical support to licensing, ... experience, preferred- 10 or More Years of pharmaceutical industry experience in Medical Affairs, strategically utilizing scientific data in various educational… more
- Merck & Co. (San Francisco, CA)
- …Company-sponsored clinical studies.Scientific Congress SupportEngages in scientific congresses and medical meetings, facilitates scientific and data exchange for ... Job DescriptionRole SummaryThe Cardiovascular & Metabolism Regional Medical Scientific Director is a credentialed (ie, PhD, PharmD, DNP, MD) therapeutic and disease… more
- Merck & Co. (Boston, MA)
- …company-sponsored clinical studies.Scientific Congress SupportEngages in scientific congresses and medical meetings, facilitates scientific and data exchange for ... Job DescriptionOur Medical Affairs team advances patient care by engaging...(GCSA).Initiates discussions with SLs and/or potential investigators that include scientific/ data exchange within our AOI to determine the alignment… more
- Merck & Co. (Rahway, NJ)
- … medical monitoring team in review and interpretation of clinical data / medical protocol-deviations in collaboration with the Clinical Director.Builds talent ... lead clinical scientist on the clinical trial team.Collaborates with the Medical Writer on clinical/scientific and regulatory documents.Partners with Study Manager… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …interactions and developing and implementing regulatory strategies with the FDA to providing medical education and collecting data to support efficacy and new ... About the Department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk...to technical complaint handling at NNI and NNCI Risk-Based Data Insights: Responsible for the creation of KPIs for… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …interactions and developing and implementing regulatory strategies with the FDA to providing medical education and collecting data to support efficacy and new ... About the Department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk...Assess the effectiveness of supported programs by reviewing outcomes data . Develop and disseminate monthly communications to internal stakeholders… more
- Merck & Co. (North Wales, PA)
- …to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for the benefit of patients and global human ... global programming standards and tools for the production of Study Data Tabulation Model (SDTM) datasets.Design and develop complex programming algorithms and… more
- Novo Nordisk Inc. (Los Angeles, CA)
- …interactions and developing and implementing regulatory strategies with the FDA to providing medical education and collecting data to support efficacy and new ... About the Department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk...of quality clinical research (patient safety, rights and wellbeing; data reliability; scientific integrity; regulatory and process compliance) for… more
- Merck & Co. (Rahway, NJ)
- Job Description Job Description As a Design Control and Risk Management Data Manager, you are a key member of the Device Development Team. Your will main ... responsibility is to develop and manage the data relationships through the development and life cycle of...Technology, Engineering, or Math (STEM) field0-2 years in the medical device or pharmaceutical industry. Required experience and skills:… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …standard data collection practices required- 4 or more years Clinical data management experience in a medical device, pharmaceutical company, or similar ... pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and… more
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