- Merck & Co. (Upper Gwynedd, PA)
- Job DescriptionThe Senior Director (Senior Principal Scientist ) has primary responsibility for the planning and directing clinical research activities involving ... marketed Oncology medicines. Our company's Oncology medicines span all phases of clinical development (pre- clinical to post-licensure). The Senior Director will… more
- Merck & Co. (North Wales, PA)
- Job DescriptionThe Director/ Principal Scientist , Regulatory Affairs Liaison , is responsible for the development and implementation of worldwide regulatory strategy ... regulatory single point-of-contact for products within Global Regulatory Affairs and Clinical Safety (GRACS) and external to GRACS.Key functions:Reports to Senior… 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 ... laboratory members, the Contract Manufacturing Organization (CMO), Labeling members and Clinical members. This position works with non-standard problems of some… more
- Merck & Co. (North Wales, PA)
- …programming activities for multiple and/or late stage drug/vaccine clinical development projects. -Accountability predominantly includes the development and ... tables, listings, figures), the span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing support.The… more
- Merck & Co. (North Wales, PA)
- Job DescriptionThe Medical Consult and Review Physician provides clinical expertise and advice to internal stakeholders and is a member of several cross-functional ... Medical Consult and Review Physician is responsible for ensuring the clinical relevance and medical accuracy of data/information in promotional materials, external… more
- Merck & Co. (North Wales, PA)
- …programming requests in close collaboration with stakeholders (statisticians/modelers) and clinical colleagues, retrieve the required data, transform the data into ... at least 7 years SAS programming experience in a clinical trial environment OR a Bachelor's degree in Computer...field plus 9 years SAS programming experience in a clinical trial environment. Required Skills and Experience: Experience in… more
- Merck & Co. (North Wales, PA)
- …support to statistical programming activities for late-stage drug/vaccine clinical development projects. Develop and execute statistical analysis and ... tables, listings, figures), the span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing support.… more
- Merck & Co. (North Wales, PA)
- …its ecosystem, under guidance of staff with extensive expertise in clinical trial A&R standards development.Provides technical consultation and analytical support to ... environment under guidance of staff with extensive expertise in clinical trial A&R standards development.Educational Qualifications:Must have a Master's degree… more
- Merck & Co. (North Wales, PA)
- …SummaryUnder the guidance of a senior leader, an Associate Principal Scientist /Associate Director, has primary responsibility for planning/managing real world and ... resource utilization and costs, physician and patient satisfaction surveys, clinical and patient reported outcomes assessments, systematic reviews and meta-analyses,… more
- Merck & Co. (North Wales, PA)
- …Description Role and Responsibilities: We are seeking an experienced talented scientist to join the Quantitative Pharmacology and Pharmacometrics - Immune/Oncology ... Systems Pharmacology (QSP) . QP2-IO team is part of the Global Clinical Development organization and has oversight over drug development aspects related to… more
- Bausch Health (Bridgewater, NJ)
- …creates it-where your skills and values drive our collective progress and impact. The Clinical Scientist will play a critical role in the design, execution, and ... reporting of clinical studies, with a strong focus on regulatory submissions,...New Drug Applications (NDAs). This position requires expertise in clinical trial data analysis, protocol development, and regulatory documentation,… more
- Taiho Oncology (Princeton, NJ)
- Sr. Manager, Clinical Research Scientist Pleasanton, CA, USA * Princeton, NJ, USA Req #457 Monday, April 7, 2025 Looking for a chance to make a meaningful ... of cancer treatment and improving patients' lives. As a Senior Manager, Clinical Research Scientist , you will play a pivotal role in our mission, leveraging your… more
- Mount Sinai Health System (New York, NY)
- …Icahn School of Medicine at Mount Sinai is seeking a Ob/Gyn Clinician Scientist for the Women's Health Research Institute.** The Women's Health Research Institute ... number of multidisciplinary institutes to conduct cutting-edge basic, translational and clinical research, and provide unparalleled clinical and training… 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
- Pfizer (New York, NY)
- …You will provide scientific oversight and support data integrity and quality of clinical trial(s) in support of the development strategy for programs within the ... Late-Stage Oncology portfolio. **Position Responsibilities** + Maintains current scientific and clinical knowledge in the specific therapeutic and disease area(s) of… more
- CVS Health (Trenton, NJ)
- …do it all with heart, each and every day. **Position Summary** Aetna's Clinical Analytics team creates innovative analytic tools to drive better healthcare outcomes. ... We're currently seeking a Data Scientist to support the development and implementation of analytic capabilities that enhance the impact of Aetna's care management… more
- Merck (North Wales, PA)
- **Job Description** The Senior Director (Senior Principal Scientist ) has primary responsibility for the planning and directing clinical research activities ... marketed Oncology medicines. Our company's Oncology medicines span all phases of clinical development (pre- clinical to post-licensure). The Senior Director will… more
- Bristol Myers Squibb (New Brunswick, NJ)
- …work and in their personal lives. Read more: careers.bms.com/working-with-us . Our Clinical Supply Operations is responsible for the supply of drug product ... administered to patients in clinical studies worldwide. In Global Product Development and Supply...This position is needed to efficiently produce GMP compliant clinical materials in support of the BMS clinical… more
- Bristol Myers Squibb (Princeton, NJ)
- …at work and in their personal lives. Read more: careers.bms.com/working-with-us . The Clinical Scientist Program Lead reports through the Clinical Science ... studies and programs. **Position Summary / Objective** + Partners with Clinical Scientist Head to plan, lead, and advance programs and talent + Serves… more
- Kelly Services (New York, NY)
- **Materials Scientist ** Kelly(R) Science & Clinical is seeking a **Materials Scientist ** for our client based in New York, NY. If you're passionate about ... and machine learning to pioneer generative materials science. This Scientist will focus on the hands-on preparation of material...the Kelly Talent Community. Why Kelly (R) Science & Clinical ? Kelly Science & Clinical is your… more
