- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …trial (small size, standard complexity in design and geographic scope). Prepares clinical section of regulatory document. Collaborates as team member with AROs/CROs. ... documents under guidance of higher level. Reviews and oversee completion of clinical trial protocols. Provides medical and/or scientific direction to Clinical … more
- Merck & Co. (Rahway, NJ)
- …the Quantitative Pharmacology and Pharmacometrics - Immune/Oncology (QP2-IO) team in the role of Associate Director QP2-IO team is part of the Global Clinical ... of drug development and effective communication skills. As a subject matter expert, the Associate Director within the QP2-IO Group will work closely with teams… more
- Merck & Co. (Rahway, NJ)
- …effective, innovative medicine.The Global Clinical Data Standards Vocabulary Specialist, Associate Director , is a subject matter expert in CDISC Controlled ... BS degree, preferably in life sciences (ie, Medical Technology, Medical Laboratory Scientist , Clinical Laboratory Scientist , Nursing), or equivalent… more
- Merck (Rahway, NJ)
- … clinical /scientific execution of clinical protocol(s). + Serves as the lead clinical scientist on the clinical trial team. + Collaborates with the ... of clinical data/medical protocol deviations in collaboration with the Clinical Director . + Builds talent and capabilities of direct/indirect team… more
- Merck (Rahway, NJ)
- …leader for the role of Distinguished Scientist which is an Executive Director level reporting to an Associate Vice President in Development Sciences & ... Clinical Supply . The Distinguished Scientist will provide scientific direction and partner with the...scientific direction and partner with the Development Sciences and Clinical Supply Digital Leadership Team to define the in… more
- Bristol Myers Squibb (Madison, NJ)
- …a preliminary conclusion. + Develops strategies for safety data collection in clinical trials to further characterize adverse events of interest. + Analyzes data ... AIMS (Asset/Indication Medical Strategy), publications, and investigator sponsored research ** Clinical Development & Post Marketing Product Support** + Leads core… more
- Pfizer (Pearl River, NY)
- …into country feasibility. **Support study team** + With supervision of medical monitor ( director /Sr director ) provides clinical input to protocol/study team ... + Provides protocol specific training to study team, investigators, clinical research associate , and others. + Interacts...etc. + **Supports the program team:** + Under supervision ( director /Sr director ) authors clinical sections… more
- Bristol Myers Squibb (Summit, NJ)
- …future therapeutics. Reporting to Senior Scientific Director Translational Medicine, the TM Associate Director will be part of the late stage TM group. The ... and Early Development organization in BMS and leads late stage clinical , pharmacological and translational research and development activities for the pipeline… more
- Pfizer (Pearl River, NY)
- …or Pfizer.com). + Provides protocol specific training to study team, investigators, clinical research associate , and others. + Interacts with healthcare ... for providing medical and scientific expertise and oversight for Clinical Trials and serves as a single point of...monitor may delegate these responsibilities to the study clinician scientist identified in the SSRP. The specific components of… more
- Merck (Rahway, NJ)
- …**Quantitative Pharmacology and Pharmacometrics -** **Immune/Oncology** **(QP2-IO)** team in the role of Associate Director QP2-IO team is part of the Global ... of drug development and effective communication skills. As a subject matter expert, the Associate Director within the QP2-IO Group will work closely with teams… more
- Bristol Myers Squibb (Berkeley Heights, NJ)
- …every treatment we pioneer. Join us and make a difference. **Purpose** The Associate Director , Biostatistics is a core member of cross-functional development ... external partners, medical monitor, protocol manager, data manager, PK scientist , and other members of the study/indication team. **Primary Responsibilities**… more
- Merck (Rahway, NJ)
- …effective, innovative medicine. The Global Clinical Data Standards Vocabulary Specialist, Associate Director , is a subject matter expert in CDISC Controlled ... BS degree, preferably in life sciences (ie, Medical Technology, Medical Laboratory Scientist , Clinical Laboratory Scientist , Nursing), or equivalent… more
