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in Boston Massachusetts JOB SUMMARY The purpose of this position is to manage multiple functions of building operations and maintenance for a facility, campus or portfolio of buildings of significant..
Other Locations:US- MA- CambridgeDescriptionCelgene is a global biopharmaceutical company leading the way in medical innovation to help patients live longer, better lives. Our purpose as a company is to discover..
The Novartis Institutes for Biomedical Research (NIBR) is seeking a highly motivated and innovative scientist to join a multi-disciplinary group, which focuses on developing and exploiting novel cell based models..
Pharmacy Manager Show me jobs like this one Job Ref: 974474636 Employer: CVS Health City: Brockton State: Massachusetts (MA) Position type: Full-Time Job Description Summary: Health is everything. At CVS..
Job Description The Associate Director CMC Project Management will be responsible for operational leadership of cross-functional CMC project sub-team(s). S/he will ensure that the CMC project(s) are defined and implemented..
CompleteRx, a leader in hospital pharmacy management and consulting has an immediate need for a Pharmacy Buyer to assist our pharmacy team in the procurement of medications and supplies for..
Clinical Research Associate - CAR-T / Oncology - Home-Based, US ICON Clinical Research • Boston MA Job #733032579 ICON is currently seeking Clinical Research Associates in ALL regions across the..
Manager Global Regulatory Affairs Chemistry, Manufacturing and Controls (CMC) - Compliance and Capit Shire • Lexington MA Job #733032880 Job Summary: The incumbent will manage change controls for the CMC..
Senior Director of Regulatory AffairsI have an exciting leadership opportunity within Regulatory Affairs for someone specialized in Regulatory Strategy and early and late stage... Requirements: Senior Director of Regulatory Affairs..
Pharmacy Manager Show me jobs like this one Job Ref: 974474365 Employer: CVS Health City: Canton State: Massachusetts (MA) Position type: Full-Time Job Description Summary: Health is everything. At CVS..
AD, Global Medical Communications Project Management You are here: Home AD, Global Medical Communications Project Management AD, Global Medical Communications Project Management Req ID: 14413 Job Category: Global Medical Affairs..
Position Summary The Associate Director, U.S. Medical Affairs Operations will lead operational excellence across all therapeutic areas in the U.S., including strategic planning, financial planning, and compliance related activities. This..
**Kelly Services is looking for a Clinical Compliance Specialist in Lexington, MA** **12 month contract** **70-72/hr depending on experience** Under the direction of the Head of R&D Clinical and Medical..
We are seeking a highly motivated and scientifically rigorous individual to lead from the the bench as a Scientist reporting to the Bioassay Team. The position will focus on protein-based..
Associate Director of Regulatory AffairsI have an exciting leadership opportunity within Regulatory Affairs for someone specialized in Regulatory Strategy and early and late stage... Requirements: Associate Director of Regulatory Affairs..
Title:Associate Director, CMC RegulatoryCompany:Ipsen Bioscience, Inc.Job Description:Position SummaryThe Associate Director of CMC Regulatory reports operationally to the Head of Quality and functionally to Head of Global CMC Regulatory. The individual..
Alexion Pharmaceuticals, Inc.Alexion is an Equal Opportunity/Affirmative Action Employer.Req ID: 14412Job Category: Global Medical AffairsLocation: Boston, MAPosting Date: September 17, 2018Attention: If you are a current Alexion employee, please apply..
Requisition ID: DIR024911 Merck & Co., Inc. Kenilworth, N.J., U.S.A. known as Merck in the United States and Canada, is a global health care leader with a diversified portfolio of..
Job Description The Project Manager, Clinical & Regulatory will identify, track, and integrate the company’s key drug development and regulatory timelines, identify dependencies and risks of key milestones, and assist..
The Role: The Regulatory Operations Manager is responsible for all operational aspects involved in the preparation and maintenance of regulatory submission documentation. This includes formatting assistance, assembly, and archival of..
The CRA II will be responsible for monitoring multiple multi-center, randomized controlled clinical studies in accordance with the protocol, standard operating procedures (SOPs), ICH-GCP, and all applicable regulatory requirements, preferably..
Clinical Trial Associate / Sr. Clinical Trial Associate Overview:The Clinical Trial Associate/Senior Clinical Trial Associate will assist in early to late clinical development operations (Phase I/II/III/IV clinical trials) in the..
The Manager, Clinical Data and Health Outcomes is the internal resource for data management and biostatistics as well as outcomes research for Organogenesis. This position is a hybrid role that..
Merck & Co., Inc. Kenilworth, N.J., U.S.A. known as Merck in the United States and Canada, is a global health care leader with a diversified portfolio of prescription medicines, vaccines..
The Purpose Novo Nordisk's Market Access and Public Affairs team engages diverse stakeholders across political and healthcare landscapes to forge solutions that drive patient access to innovative products. We strive..