- 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)
- …risk management techniques to positively support and influence clinical and commercial combination product development and launches.Principal ResponsibilitiesLead ... ensure full integration of the device development activities with the clinical , regulatory, formulation, commercial and other key company functions.Represent Device… 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)
- …and risk management techniques to positively support and influence clinical and commercial combination product development and launches. **Principal ... to ensure full integration of the device development activities with the clinical , regulatory, formulation, commercial and other key company functions. + Represent… 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
- Pfizer (Pearl River, NY)
- …or Pfizer.com). + Provides protocol specific training to study team, investigators, clinical research associate , and others. + Interacts with healthcare ... is preferred. + Provides protocol specific training to study team, investigators, clinical research associate , and others. + Interacts with healthcare… 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)
- …procedural and scientific subject matter expertise to steer clinician medical monitors, clinician clinical scientists, clinical scientist leads, and other ... or Pfizer.com) + Provides protocol specific training to study team, investigators, clinical research associate , and others. + Interacts with healthcare… 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)
- …with talented and dedicated colleagues while developing and expanding your career. The Clinical Director (Principal Scientist ) has primary responsibility for ... medicines span all phases of clinical development (pre- clinical to post-licensure). The Director will manage...clinical development projects; and + Assist the Senior Director , Executive Director , and/or Associate … more
- Hackensack Meridian Health (Nutley, NJ)
- …of 50 articles in scientific journals or book chapters while in rank as an Associate Scientist , Associate . Professor or equivalent rank. The candidate must ... **Overview** The **Scientific Director -Center for Discovery and Innovation** will serve as...to the highest ethical standards of research, and facilitate clinical translation of research efforts. This role will work… 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