- Merck & Co. (Rahway, NJ)
- Job DescriptionPosition Description: Associate Director, Clinical Scientist This position drives scientific planning, strategy and execution of Phase 1-4 ... the clinical trial team.Collaborates with the Medical Writer on clinical /scientific and regulatory documents.Partners with Study Manager on study… more
- Genmab (Plainsboro, NJ)
- …is essential to fulfilling our purpose.The Role & Department As a Senior Programming Associate or Programming Manager , you will be in the Statistical Programming ... leading a small team to complete various programming efforts within a clinical trial.You will be responsible for ensuring integrity, consistency, and adherence to… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Associate Principal Scientist, General Medicine Publications Medical Writing, works with scientists in our company's Research Labs and external ... and posters/oral presentations that report results from our company's General Medicine clinical trial program, as well as select early-stage development projects and… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- About the Department The Clinical , Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the ... organization. From health -care-provider interactions and developing and implementing regulatory strategies with...staff members of Medical Information (MI) report to the Associate Director. The Associate Director communicates medical… more
- Genmab (Plainsboro, NJ)
- …as trial responsible statistician with responsibilities as described below. The Associate Director contributes to clinical development strategies and ... be our best, and authentic is essential to fulfilling our purpose.The RoleThe Associate Director acts as a statistical expert supporting the clinical development… more
- Aequor (New York, NY)
- …tools in health services research is required, eg, literature review, clinical data interpretation and claim data analysis Knowledge of data science desirable ... Job Description: This is a full-time 12-month consultant/research associate (RA) position in 's Pneumococcal Vaccine Global Access Strategy and Pricing (GASP) Team.… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …technical teams in preparation of submission documents to include clinical trial applications/amendments (eg, IND, IMPD, IB) and marketing applications/supplements ... this position acts as the company liaison with the Health Authority (eg, US FDA and EU EMA) for...members, the Contract Manufacturing Organization (CMO), Labeling members and Clinical members. This position works with non-standard problems of… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …plans with minimal supervision and contributes to documents submitted to Health Authorities globally with some supervision. This position also guides contract ... Statistical Analysis Plan (SAP), Statistical Analysis, Results Interpretation, and clinical study report (CSR): Leads statistical activities for complex studies… more
- CHRISTUS Health (Wake Village, TX)
- …coordinating, processing, screening, and documentation of patient entry into the CHRISTUS Health System. The Registered Nurse Clinical Care Coordinator will ... and active participation in fulfilling the Mission of CHRISTUS Health . It is expected that the associate ...clinical information for patients upon entry into the health system to determine appropriate placement and patient class… more
- CHRISTUS Health (Tenneryville, TX)
- …Education/Skills Associate 's Degree in Nursing Experience 4 years of clinical nursing and 1 year in a supervisory role preferred Licenses, Registrations, ... Description Summary: Directs the operation of clinical programs and promotes quality services for the community and patients. Responsibilities: * Develops,… more
