- Parexel (Providence, RI)
- …success, we are expanding our esteemed Medical Sciences Team and seeking an Associate / Medical Director to support the growth of our Global Immunology and ... Inflammation Therapeutic Franchise. As an Associate / Medical Director , you...the development and/or review of study documents, such as clinical protocols, Medical Monitoring Plans (MMP), integrated… more
- Parexel (Providence, RI)
- …activities associated with audits and regulatory inspections in liaison with LSAD and Clinical Quality Associate Director (CQAD). + Ensures timely ... SE Region - FL** **ONCOLOGY preferred** **Job Purpose:** The Clinical Research Associate (CRA) has local responsibility...other CRAs and the Local Study Team/ Local Study Associate Director (LSAD) to ensure that study… more
- GRAIL (Providence, RI)
- …and we are using the power of next-generation sequencing (NGS), population-scale clinical studies, and state-of-the-art computer science and data science to overcome ... + **Experience** + Minimum of 10 years of experience in regulatory, development, clinical affairs, quality, or program management within the IVD, medical device,… more
- Parexel (Providence, RI)
- **Job Purpose:** The Senior Clinical Research Associate I (Sr. CRA) is responsible for the site management, site monitoring and close-out of assigned clinical ... action (CAPA) development and checks, when applicable **Collaboration** + Reports to Director of Clinical Site Operations (DCSO) or Director … more
- Parexel (Providence, RI)
- …activities associated with audits and regulatory inspections in liaison with LSAD and Clinical Quality Associate Director (CQAD). + Ensures timely ... The Senior Clinical Research Associate (SrCRA) has local...other CRAs and the Local Study Team/ Local Study Associate Director (LSAD) to ensure that study… more
- Sumitomo Pharma (Providence, RI)
- …** Medical Director , Clinical Development - Oncology** . The associate medical director is responsible for the leadership, development, and ... management of clinical studies while building and maintaining relationships with investigators...of the overall product development plan, based on strong medical and scientific principles, knowledge of compliance and regulatory… more
- Otsuka America Pharmaceutical Inc. (Providence, RI)
- … needs and nutraceutical products for the maintenance of everyday health. As an Associate Director , Biostatistician, you will be a champion of Otsuka's culture ... responsible for providing statistical expertise/input in the drug development including clinical development plan and regulatory submission strategy. This is a… more
- Sumitomo Pharma (Providence, RI)
- …seeking a dynamic, highly motivated, and experienced individual for the position of ** Associate Director , Regulatory Affairs (Oncology).** The Associate ... with colleagues, fostering collaboration, and idea sharing + Reviews nonclinical, clinical and CMC documentation (eg nonclinical study reports, clinical … more
- Otsuka America Pharmaceutical Inc. (Providence, RI)
- **Job Summary** The Associate Director , Global Product Quality - Biologics is responsible for directing quality oversight of clinical and commercial products ... biologics-specific GMP requirements. This role has global responsibility for directing clinical and commercial product quality to ensure global supply for Otsuka's… more
- Otsuka America Pharmaceutical Inc. (Providence, RI)
- The Associate Director , Strategic Planning & Operations will support the assets of varying lifecycle stages in the relevant therapeutic area portfolio. This role ... in driving operational excellence and innovation within our Global Medical Affairs organization, with a specific focus on the...are in place. This position reports directly into the Director , Strategic Planning Lead, who in turn reports into… more
