- Sanofi Group (Cambridge, MA)
- …CRD is to: + Provide medical expertise in the Study team to conduct the clinical studies from early phases to LCM programs + Collaborate with other medical ... medical input & support for all activities related to clinical studies conduct such as answers to...Study committee Charters + Collaborate on key medical and clinical questions with the Global feasibility manager … more
- Sanofi Group (Waltham, MA)
- …Team. He/She will assume responsibility for methodological and statistical aspects of pre- clinical and/or non- clinical studies , with general direction from ... bring hope to patients and their families. The Biostatistics Manager of the TED (Translational and Early Development) team...and assumptions of in vivo or in vitro preclinical studies and/or research, clinical and analytical (CMC)… more
- Bristol Myers Squibb (Cambridge, MA)
- … Clinical Scientist function provides scientific expertise necessary to design and deliver clinical studies and programs. + Will be responsible for design and ... execution of assigned clinical trial activities and work closely with ...co-lead study team meetings in partnership with GDO protocol manager and collaborate with cross-functional study team members +… more
- Takeda Pharmaceuticals (Boston, MA)
- …our strategic partners and other vendors to ensure the effective execution of the clinical studies on time, with high quality and within agreed budget. ... program execution. Works closely with COMs, Global Program Manager (GPM), and Finance to ensure on a regular...clinical study/project management. Experience must include early phase clinical studies /Phase 2 studies or… more
- Beth Israel Lahey Health (Burlington, MA)
- …providing mentoring, direction and guidance to research staff (eg, Clinical Research Coordinators). **Job Description:** **Essential Duties & Responsibilities** ... Has direct knowledge and experience in the implementation of all aspects of clinical trials research adhering to Research SOPs, GCP compliance and FDA regulations.… more
- Parexel (Boston, MA)
- …for the preparation, initiation, monitoring, and closure of assigned sites in clinical studies , in compliance with Client Procedural Documents, international ... SE Region - FL** **ONCOLOGY preferred** **Job Purpose:** The Clinical Research Associate (CRA) has local responsibility for the...(CRA) has local responsibility for the delivery of the studies at allocated sites and is an active participant… more
- Parexel (Boston, MA)
- …for the preparation, initiation, monitoring, and closure of assigned sites in clinical studies , in compliance with Client Procedural Documents, international ... The Senior Clinical Research Associate (SrCRA) has local responsibility for the delivery of the studies at allocated sites and is an active participant in the… more
- Olympus Corporation of the Americas (Westborough, MA)
- … Affairs to execute clinical strategy activities and oversee aspects of clinical studies in support of clinical evidence generation strategies across ... Risk Management, Quality and Regulatory Affairs, and investigational sites. + Ensures clinical studies are conducted in compliance with relevant Olympus… more
- Tufts Medicine (Boston, MA)
- … research budgets in accordance with policies. 2. With support from their manager , reviews clinical research protocols for resource and financial implications ... of facts, policies and practices. **Job Overview** This position supports clinical investigators, research administrators, clinical trials, and study teams… more
- Beth Israel Lahey Health (Boston, MA)
- …in clinical research projects, enrolling research subjects onto these studies , monitoring protocol implementation, completing required forms , data entry, data ... As needed, may function in areas/clinics performing job duties related to clinical research studies . **Required Qualifications:** + Bachelor's degree required. +… more