- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- …The Executive Director TA Operations Leader is responsible for directing clinical operations activities and decisions including quality , timelines and costs ... of clinical research studies in accordance with applicable regulations, ICH/ GCP regulations and company Standard Operating Procedures (SOP's) within assigned TA… more
- Otsuka America Pharmaceutical Inc. (Princeton, NJ)
- …Strategic R&D Sourcing strives to maximize contract value while maintaining strict quality standards. The Senior Director role is responsible for setting ... actuals vs. forecasts in collaboration with Finance and key functional partners ( Clinical Management, Regulatory Affairs, Global Quality , Data Management, Global… more
- Sanofi Group (Morristown, NJ)
- …that leverage digital tools & technologies for advanced medical and clinical research opportunities. **Compliance and Quality Assurance** + Accountable ... **Job title** : Global Medical Director , Evidence Generation - Insights and Strategy **Location:**...all evidence generation activities comply with regulatory requirements, Good Clinical Practice ( GCP ), and company policies. +… more
- Sanofi Group (Morristown, NJ)
- …for ensuring all evidence generation activities comply with regulatory requirements, Good Clinical Practice ( GCP ), and company policies. + In charge of ... **Job title** : Global Medical Director , Evidence Generation - Innovation & Partnerships **Location:**...in patient and scientific knowledge and insights to improve clinical care. We do this by generating and curating… more
- Ascendis Pharma (Princeton, NJ)
- …a dynamic workplace for employees to grow and develop their skills. Associate Director , Global Patient Safety Medical Science reports to Head of GPS Medical Science. ... activities. + Conducts medical review, assessment, and approval of ICSRs from clinical trials and post-marketing. + Ensures that all safety reports received from… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …to optimize laboratory data processes, technology, and standards. This position ensures quality delivery of laboratory data for clinical trials, clinical ... develops and proposes strategies for laboratory data ensuring all clinical trials meets quality requirements and best...expertise to promote and implement best practices across the Clinical Trial lifecycle. - Applies GCP principles… more
- J&J Family of Companies (Titusville, NJ)
- …with excellent knowledge and understanding of design control process, analytical and clinical validation, manufacturing, GCP , GLP, and GMP requirements, Global ... for humanity. Learn more at https://www.jnj.com **Job Function:** Discovery & Pre- Clinical / Clinical Development **Job Sub** **Function:** Clinical … more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …of group members. This position also monitors trends in functional performance via quality , time, and cost indicators, and develops plans and leads the execution for ... for projects/studies. This position has sufficient understanding of regulations and GCP requirements for drug development, advanced knowledge of Electronic Data… more
- Prime Healthcare (Newark, NJ)
- …and Work Experience + Minimum Bachelors in Health Related Sciences or equivalent + Clinical Trials HIPAA certification + Knowledge of ICH/ GCP , FDA and IATA ... an award-winning team of dedicated professionals committed to our core values of quality , compassion and community! Saint Michael's Medical Center, a member of Prime… more
- Bristol Myers Squibb (Princeton, NJ)
- …is essential to the study level operationalization of the eCOA capability for BMS clinical trials and directly contributes to the BMS R&D pipeline. This role reports ... to the Associate Director , eCOA Management within GDM and is a full-time,...Providing leadership for the operationalization of eCOA instruments for clinical trials, facilitating the end to end process, providing… more