Drug Safety Jobs in Massachusetts
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Search Results - Drug Safety Jobs in Massachusetts
Collegium Pharmaceutical-Stoughton (MA)
medications.
POSITION OVERVIEW
The Senior Associate, Drug Safety will be responsible for executing Adverse Event and Pharmacovigilance activities as required by FDA regulations. This role coordinates Adverse Event and Pharmacovigilance activities...
mindmatch.ai -
Leading Age-Waltham (MA)
Senior Medical Director/Global Safety Officer - Drug Safety and Pharmacovigilance
Job Overview:
The Senior Medical Director/Global Safety Officer (GSO) will work closely with the DSPV leadership team and will provide strategic safety oversight...
appcast.io -
Biogen-Cambridge
Job Description
About This Role
At the Principal Data Science level, this person is viewed as an expert within Technology, Analytics and Data Insights (TADI) and provides solutions to the group and the Drug Safety, Global Regulatory and Research...
resume-library.com -
Page Mechanical Group, Inc.-Boston
for each Product Development Team and coach/supervise the staff in the execution of their responsibilities to the team as they pertain to drug safety including protocol input, Investigator Brochure input, annual reports, signal detection and the key safety...
appcast.io -
BioPharma Consulting JAD Group-Cambridge
to drug safety risk management.
Manage cross-functional briefings and technical meetings for project stakeholders and customer representatives.
Demonstrates diplomacy, reasoning, and problem-solving.
Negotiation skills encouraging discussion and driving...
resume-library.com -
Page Mechanical Group, Inc.-Boston
responsible for ensuring the highest standards of drug safety and compliance within Aveo Oncology. This role involves overseeing the quality management of pharmacovigilance activities and managing strategic alliances with external partners.
The Director...
appcast.io -
Integrated Resources, Inc-Cambridge
Education: Degree in a medical or healthcare related discipline (MSN RN, PharmD, Physician Assistant, MD) is required
Experience: A minimum of three to five years in the pharmaceutical industry with experience in drug safety/pharmacovigilance.
Strong...
resume-library.com -
Klein Hersh International-Boston
required.
• Minimum of 10 years of global experience in drug safety within the biotechnology or pharmaceutical industry.
• In-depth knowledge of FDA safety regulations, ICH Guidelines, EU GVP, and other global safety regulations.
• Deep understanding...
appcast.io -
Cambridge
Degree in a medical or healthcare-related field.
• Experience in drug safety or pharmacovigilance.
• Ability to improve business processes and develop practical solutions.
• Familiarity with safety databases and signaling tools.
• Understanding...
pharmiweb.jobs -
Biogen-Cambridge
populations and burden of disease throughout the drug development life cycle. This is accomplished by synthesizing existing knowledge as well as designing and conducting studies related to disease prevalence and drug safety and effectiveness.
The group...
resume-library.com -
Deciphera Pharmaceuticals, Inc-Waltham (MA)
and products. Responsible for keeping upper management informed of safety issues. May represent Deciphera, Drug Safety and Risk Management at internal and external meetings. May be appointed as the Safety lead for a specific compound / product.
The successful...
appcast.io -
Biogen-Cambridge
Job Description
About This Role
At the Associate Director level, this person is viewed as a leader and expert within Technology, Analytics and Data Insights (TADI) and provides leadership to the group and the Drug Safety, Global Regulatory...
resume-library.com -
Pfizer-Cambridge
into the therapies and vaccines that matter most. Whether you are in the discovery sciences, ensuring drug safety and efficacy or supporting clinical trials, you will apply cutting edge design and process development capabilities to accelerate and bring the best...
dejobs.org -
Bicycle Therapeutics-Cambridge
lead on the clinical study team
Author and review clinical documents, including protocols, amendments, informed consent forms, clinical study reports, investigator brochures, drug safety update reports, and clinical development plans
Lead medical data...
resume-library.com -
Katalyst Healthcares & Life Sciences-Waltham (MA)
and oversight of assigned studies including sign off document as it impacts medical coding review, product approval, analysis of coded data for safety review and signal detection and patient safety.
Identifies when terms or drug names are inadequate, ambiguous...
resume-library.com -
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