- BeOne Medicines (Boston, MA)
- …practices. Minimum Requirements - Education and Experience: For Senior Director Level: MD, PharmD ., PhD , or DO, within a clinical and/or scientific profession ... experience and/or success within other biotech/pharmaceutical companies For Director Level: MD, PharmD ., PhD , or DO, within a clinical and/or scientific… more
- Pfizer (Boston, MA)
- …as needed **BASIC QUALIFICATIONS:** + Bachelor's degree in a Health Science required + PharmD , PhD , or equivalent terminal doctoral degree (eg, Doctor of Nursing ... Practice, Doctor of Physical Therapy) highly preferred + Relevant experience required: PharmD / PhD with 6 years of experience, MBA/MSc with 8 years of experience,… more
- Takeda Pharmaceuticals (Boston, MA)
- …EXPERIENCE, KNOWLEDGE AND SKILLS:** **Required:** + Advanced scientific degree (MD, or PhD , or PharmD ) + Minimum of 12 years related/relevant experience ... submissions/approvals for multiple NMEs Advanced degree in science field (MD, PharmD or Ph.D.) + Broad business/enterprise orientation with proven matrix leadership… more
- Astrix Technology (Boston, MA)
- …and insights in the appropriate systems. **Qualifications** + Education: Advanced degree ( PharmD , PhD , MD, or equivalent) in a relevant scientific discipline. ... + Experience: Minimum of 2 years in a field-based medical affairs role within the pharmaceutical, biotechnology, or medical device industry. + Scientific Expertise: Deep understanding of therapeutic areas relevant to the company's portfolio, with the ability… more
- Bayer (Cambridge, MA)
- …incumbent who possesses the following: **REQUIRED QUALIFICATIONS:** + University degree (MD, PharmD , PhD ) in Biochemistry, Molecular Biology, Genetics, or a ... related field; + Demonstrated leadership in drug development, particularly in CVR indications; + Strong scientific laboratory skills with a profound knowledge of experimental systems and technologies for molecular biomarker identification; + Excellent… more
- Orchard Therapeutics (Boston, MA)
- …with a relevant post-graduate qualification (eg, MRCP, MRCS, MFPM, MD). Experienced candidates with an advanced degree (eg, PharmD ., Ph.D.) will also be considered. ... Location: Boston, MA or London, UK Reporting to: Vice President, Clinical Development Job Summary Orchard Therapeutics is a global biotechnology gene therapy company dedicated to transforming the lives of people affected by rare diseases through the… more
- Sumitomo Pharma (Boston, MA)
- …MSL experience in oncology/hematology preferred. + Advanced degree in medical science (MD, PharmD , or PhD ) is strongly preferred. Candidates without an advanced ... degree are required to have at least 5 years of industry MSL experience, and 6-10 years overall related experience. The base salary range for this role is $175,680 to $219,600. Base salary is part of our total rewards package which also includes the… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …a matrix structure, in Medical Affairs roles, + A higher education degree (MD, PharmD , PhD ), or master's degree in biomedical discipline or equivalent + CMPP ... certification (preferred) + Prior experience in immune-mediated inflammatory diseases (preferred, especially in immunoglobulin A nephropathy and immune thrombocytopenia) + Critical thinker able to understand complex disease states, datasets and strategic… more
- Takeda Pharmaceuticals (Boston, MA)
- …scientific discipline strongly preferred + Advanced degree in a scientific discipline ( PharmD / PhD /MD) strongly preferred + 12+ years of pharmaceutical industry ... experience. This is inclusive of 10 years of regulatory experience or combination of 8+ years regulatory and/or related experience. + Experience in reviewing, authoring, or managing components of regulatory submissions. + Expert knowledge of drug development… more
- Sanofi Group (Cambridge, MA)
- …least 3 years of relevant Regulatory Affairs experience in the United States or Advanced degree ( PharmD , PhD , MD or DVM) with at least 2 years of regulatory or ... relevant + Significant track record of US regulatory expertise required (demonstrated experience with preparation of NMAs, LCM activities, briefing documents) and negotiating with the US FDA. + Experience with acceleration pathways (Orphan Drug, Breakthrough… more