- Parexel (Boston, MA)
- The Clinical Biomarker Specimen Specialist works collaboratively with the Clinical Biomarker Operations Manager , Study Managers, and Scientific ... from collection through testing and final sample disposition. This role requires clinical study , specimen management, and project management experience. As well… more
- ACROBiosystems Inc. (Boston, MA)
- …validation, candidate drug screening and optimization, CMC development, preclinical and clinical studies , commercial production, and companion diagnostics. We ... cross-functional collaboration and continuous learning. Job Summary The Regional Account Executive/ Manager (Junior to Senior level) role is responsible for leading… more
- Sanofi (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 and ... 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 (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 ... and assumptions of in vivo or in vitro preclinical studies and/or research, clinical and analytical (CMC)...Selects statistical methodology to support the objectives of the studies , Drives risk assessment for study conclusions… more
- Novo Nordisk Inc. (Boston, MA)
- …products and services for their patients Maintain knowledge of the most recent clinical studies to inform customers and address questions, concerns, and ... CMCS I -Ecosystem I reports to the Ecosystem Business Manager . The CMCS I -Ecosystem I also must work...volume Utilize discretionary budget for maximum impact on sales Clinical Understanding Deep understanding of cardiometabolic disease state and… more
- Sanofi (Cambridge, MA)
- …and/or clinical lead in the medical/scientific contribution for the clinical studies on activities pertaining to the Study Medical Manager (SMM) ... clinical development plans and trial set-up to clinical study report in compliance with quality...in the therapeutic area. Under the guidance of his/her manager in the Therapeutic Area department, he/she collaborates with… more
- Parexel (Boston, MA)
- …for the preparation, initiation, monitoring, and closure of assigned sites in clinical studies , in compliance with Client Procedural Documents, international ... (CRA) has local responsibility for the delivery of the studies at allocated sites and is an active participant...escalating systematic or serious quality issues, data privacy breaches, Clinical Study Protocol (CSP) or ICH-GCP compliance… more
- Parexel (Boston, MA)
- …Study Operations Manager (SOM) + When required Partners with other Study Team members (eg Clinician, Recruitment Specialist, Clinical Data Scientist) + ... + Demonstrated knowledge in disease and technical areas pertaining to clinical studies , including knowledge of company direction, investigational product(s),… more
- Parexel (Boston, MA)
- …for the preparation, initiation, monitoring, and closure of assigned sites in clinical studies , in compliance with Client Procedural Documents, international ... (SrCRA) has local responsibility for the delivery of the studies at allocated sites and is an active participant...escalating systematic or serious quality issues, data privacy breaches, Clinical Study Protocol (CSP) or ICH-GCP compliance… more
- Parexel (Boston, MA)
- …champion, etc.). **Skills:** + Strong understanding of the different operational aspects of clinical study conducts in different regions across the world, which ... **Homebased US** As a Proposal Manager with Parexel you are in a client...(RFP) process + Receives and analyzes RFP documentation including study protocol or synopsis and ensures all appropriate Subject… more
