- AbbVie (North Chicago, IL)
- …key regulatory discussions. + Ensures adherence to Good Clinical Practices, pharmacovigilance standards, standard operating procedures and to all other quality ... standards in conducting research. Qualifications Qualifications + Medical Doctor (MD), Doctor of Osteopathy (DO), or non-US equivalent of MD degree with relevant therapeutic specialty in an academic or hospital environment. Completion of a residency program… more
- Pfizer (Frankfort, KY)
- …alternate site clinic negotiations, and formulary inclusion for biosimilars. + Pharmacovigilance and post-market safety monitoring. + Preferred: + Oncology and/or ... Immunology & Inflammation therapeutic area expertise. + Proven success engaging Academic Medical Centers, Integrated Delivery Networks (IDNs), and large group practice community accounts. + Strong understanding of evolving healthcare landscape in US, including… more
- AbbVie (North Chicago, IL)
- …responses and discussions. + Ensures adherence to Good Clinical Practices, pharmacovigilance standards, standard operating procedures and to all other quality ... standards in conducting research. Qualifications Qualifications + Medical Doctor (MD), Doctor of Osteopathy (DO) or non-US equivalent of MD degree with relevant therapeutic specialty in an academic or hospital environment. Completion of a residency program… more
- AbbVie (North Chicago, IL)
- …key regulatory discussions. + Ensures adherence to Good Clinical Practices, pharmacovigilance standards, standard operating procedures and to all other quality ... standards in conducting research. Qualifications + Medical Doctor (MD), Doctor of Osteopathy (DO), or non-US equivalent of MD degree with relevant therapeutic specialty in an academic or hospital environment required. Completion of a residency program strongly… more
- AbbVie (Irvine, CA)
- …for key regulatory discussions. *Ensures adherence to Good Clinical Practices, pharmacovigilance standards, standard operating procedures and to all other quality ... standards in conducting research. Qualifications *Bachelors degree in the sciences; advanced degree (eg, MS, PhD, OD, MD, PharmD) preferred. *At least 8 years of product development experience with 5 years of experience in consumer eye care in the… more
- Arvinas (New Haven, CT)
- …research physician + Partner with Clinical Operations, Translational Medicine, Pharmacovigilance , Data management and other functional team members at assure ... quality and timely study conduct and monitoring + Provide support as needed for clinical and scientific issues that may arise during study execution + Work closely with biostatisticians and programmers to plan analyses of clinical data + Support data summaries… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …Quality/Compliance experience. + Advanced knowledge of clinical research (GCP), pharmacovigilance (GVP) and medical throughout R&D and commercialization, and ... relevant regulations. + Preferably with experience in strategic roles involving quality systems and clinical portfolio oversight, large-scale audit programs, regulatory inspection management, investigation and remediation activities on a global level and… more
- Astellas Pharma (Northbrook, IL)
- …statistics, medical affairs statistics, real-world evidence (RWE), safety/ pharmacovigilance (PV) statistics, statistical programming, biomarker statistics, and ... advanced analytics. The role ensures consistency and scientific excellence across studies, indications, and evidence types-while enabling innovation in statistical methodology, clinical development optimization, and external engagement. The GSTATL plays a key… more
- Ascendis Pharma (Palo Alto, CA)
- …about patient safety and ready to help lead a fast-paced, global pharmacovigilance organization? Ascendis Pharma is seeking an experienced Program Safety Lead to ... role The role of Program Safety Lead is a director level position here at Ascendis and this Lead...a pivotal role as the Program Safety Lead and pharmacovigilance expert for the Ascendis' endocrinology pipeline. As a… more
- Merck (Rahway, NJ)
- …our company and will be a key growth driver for our company. The Director , Global IBD Patient Strategy is responsible for shaping the global strategy and framework ... patient access and are competitive with existing market offerings. The Director will partner cross-functionally with global and ex-U.S. commercial, medical, access,… more