- Daiichi Sankyo, Inc. (Bernards, 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)
- Job DescriptionThe Associate Principal Scientist , Device Risk Management Lead, is a crucial member of our team, responsible for spearheading risk management ... through launch and post-market surveillance. Key Responsibilities and Activities: The Associate Principal Scientist , Device System - Device Risk Management… more
- Merck & Co. (Rahway, NJ)
- …barriers to reimbursement and market access, and provide input into clinical , regulatory, payer/access, marketing and evidence generation strategies and programs.In ... Pharmacy (AMCP) dossiers for US payers, and Global Value Dossiers.Develop supplementary clinical data package in close partnership with markets and HTA statistics… 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)
- Job DescriptionThe Global Clinical Data Standards Vocabulary Specialist, Associate Director , is a subject matter expert in CDISC Controlled Terminology and ... BS degree, preferably in life sciences (ie, Medical Technology, Medical Laboratory Scientist , Clinical Laboratory Scientist , Nursing) or equivalent… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …and Academia. L ine management responsibility of Director / Associate Director Global Safety Lead, Senior Global Safety Scientist (s)/Global Safety ... and Seattle reflect the full R&D continuum, from early research through late-stage clinical development. Here, we are building for the future, creating a distinct… more
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- … Director to join out Oncology Clinical Development department. The Associate Director Clinical Sciences leads in the development, evaluation, ... scientific integrity and interpretation of study data of a clinical development program. The Associate Director...may include the following: + May function as lead Clinical Scientist for program, and/or as delegate… more
- Regeneron Pharmaceuticals (Tarrytown, NY)
- …Associate Director to join our Clinical Development team. The Associate Director Clinical Sciences leads in the development, evaluation, planning ... Scientists or Therapeutic area Lead Clinical Scientist and collaborates closely with Medical Director (s)to...on clinical studies and programs. **As an Associate Director , a typical day may include… more
- 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
- University of Colorado (Aurora, CO)
- **Assistant or Associate Dean and Director , Medical Scientist Training Program** **Description** **University of Colorado Anschutz Medical Campus** ... Associate Professor and/or Professor** **Working Title: Assistant or Associate Dean and Director , Medical Scientist...MSTP students and integrate best practices in research and clinical training. + Actively contribute as a member of… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …inspire you and empower you to shine? Join us as an Associate Medical Director in our Takeda R&D Physician Scientist Accelerator Program in our Cambridge, MA ... contributor to our inspiring, bold mission and high-performing culture. **OBJECTIVES:** The Associate Medical Director will be joining the Takeda R&D Physician… more
- Merck (Rahway, NJ)
- **Job Description** The Associate Principal Scientist , Device Risk Management Lead, is a crucial member of our team, responsible for spearheading risk management ... through launch and post-market surveillance. **Key Responsibilities and Activities:** The Associate Principal Scientist , Device System - Device Risk Management… more
- Johns Hopkins University (Baltimore, MD)
- …Engineering is looking for a highly motivated. proactive, organized, and diplomatic Executive Director (ED). NTH is one of two recipients of an NIH-funded Blueprint ... Incubator award. This program is managed collaboratively with CINTA. The Execuitive Director will primarily be responsible for overall execution of all core… more
- New York University (New York, NY)
- …Clinic; Serve as a member of the Executive Committee; Assist the Program Director , faculty, clinical consultants and matriculants with various elements of ... exercising independent judgment as deemed appropriate through consultation with Program Director ; conducts community outreach to promote Clinic services and attract… more
- Lilly (Indianapolis, IN)
- …anticipated wage for this position is $63,000 - $140,800 The Eli Lilly Clinical Diagnostics Laboratory (ELCDL) supports pre-screening, clinical trial, and assay ... the overall business strategy and corporate portfolio objectives. These clinical tests may be used in clinical ...to support regulatory submissions. Are you a Medical Laboratory Scientist (MLS) or Medical Technologist (MT) that is responsible… more
- Merck (Rahway, NJ)
- …barriers to reimbursement and market access, and provide input into clinical , regulatory, payer/access, marketing and evidence generation strategies and programs. + ... (AMCP) dossiers for US payers, and Global Value Dossiers. + Develop supplementary clinical data package in close partnership with markets and HTA statistics group… more
- AbbVie (North Chicago, IL)
- …LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description The position of Associate Scientist , Toxicology Study Coordinator is in the Preclinical ... will be filled at level commensurate with extent of education, experience, and accomplishment. Associate Scientist I or Associate Scientist II Additional… more
- Cedars-Sinai (Los Angeles, CA)
- …Cancer (CSC) Director for OncoBiobank Shared Resource (OBSR), the Associate Biomedical Scientist will oversee the operation, maintenance, and development ... materials science, engineering preferred). **Req ID** : 7677 **Working Title** : Associate Biomedical Scientist **Department** : Cancer - Shared Services… more
- Johns Hopkins University (Baltimore, MD)
- …statistical pipelines and cutting-edge quantitative science methodologies for state-of-art clinical studies. Thus, the members of the Division of Quantitative ... strong mentorship and a career-path for faculty statisticians. The Data Scientist collaborates independently with principal investigators in statistical design and… more
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- …early and/or late phase development. The Manager reports to either Associate Director or Director , Clinical Sciences and collaborates closely with ... The Manager, Clinical Sciences, Hematology leads in the development, evaluation,...leads in the development, evaluation, planning and execution of clinical studies and ensures scientific integrity and interpretation of… more
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