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Keywords: Medical Affairs Project Manager Associate Director (Hybrid), Location: Boston, MA

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Medical Affairs Project Manager Associate Director (Hybrid)

Job Description General Summary: The Project Management Associate Director will be responsible for the integration... equivalent combination of education and experience, in project management preferably within Medical Affairs, Clinical Development...

Location: Boston, MA
Posted Date: 28 Mar 2025

Biostatistics Associate Director (HYBRID)

Job Description General Summary: The Biostatistics Associate Director will perform sophisticated scientific... statistical analyses in support of the company's Global Medicines Development and Affairs area with minimal guidance and mentoring...

Location: Boston, MA
Posted Date: 19 Mar 2025

US Compliance Business Partner (Research & Development & Pain), Associate Director (Hybrid)

Job Description US Compliance Business Partner (Research & Development & Pain), Associate Director (Hybrid... and medical affairs activities, including research and interpretation of the Food, Drug, and Cosmetic Act; FDA regulations...

Location: Boston, MA
Posted Date: 21 Feb 2025

Manager, Global Regulatory Strategy US & Canada - Neuroscience (Onsite Hybrid)

. Responsibilities: Responsible for a product(s) within Neuroscience and supports the Manager (Senior Manager, Associate Director... serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives...

Company: AbbVie
Location: Cambridge, MA
Posted Date: 03 Apr 2025

Associate Director, Market Access Strategy - T1D

Job Description Associate Director, Market Access Strategy - T1D Location: Boston, MA (3 days onsite, 2 days remote.... This role will work closely with Brand Marketing, Medical Affairs, Public Affairs, HEOR, Payer Account Management, and Field...

Location: Boston, MA
Posted Date: 21 Feb 2025

QA Associate Director, CMC Regulatory Submission QC and Audit

Job Description The QA Associate Director, CMC Regulatory Submission QC and Audit, is responsible for the audit.../review of all regulatory submissions in support of submission readiness for small molecule, biologics, and medical devices...

Location: Boston, MA
Posted Date: 18 Jan 2025

Director, Clinical Trial Management

-paced and expanding Global Clinical Operations (GCO) organization, and may also manage individuals at the Associate Director...Job Description General Summary: The Director, Clinical Trial Management is responsible for the planning, oversight...

Location: Boston, MA
Posted Date: 16 Mar 2025