Search Results: 23 vacancies
...VRC), Clinical Trials Program (CTP).
Requirements:
-Oversee operational aspects of the VRC Clinical Trials Program (CTP) Pharmacovigilance (PV) Team, which leads the process for safety signal management activities, and ensures the detection, assessment, understanding...
Suggested
Visa sponsorship
Flexible hours
...Job Description
Job Description SAFETY & PHARMACOVIGILENCE SPECIALIST
~6 month temp to hire
~ Hybrid - Bethesda, MD
~ Medical experience is a must; BSN, Pharm D. but prefer MD or DO
~ Prefer someone who has worked in industry
~ Will accept foreign medical...
Suggested
Temporary work
...Center for Drug Evaluation and Research (CDER), located at Silver Spring, Maryland. This project is located in the Office of Pharmacovigilance & Epidemiology (OPE), Office of Surveillance and Epidemiology (OSE).
Research Project: The project aims to better understand...
Suggested
Permanent employment
Full time
Contract work
...after every release cycle.
Experience on Health science /life sciences project is greatly desired. Specifically, experience on pharmacovigilance related domains is greatly preferable over experience in other non-health science/life sciences domains.
Experience and...
Suggested
Contract work
Local area
Immediate start
...Piper Companies (Health & Sciences) is seeking motivated candidates for a Medical Monitor and/or Safety & Pharmacovigilance Specialist opportunity in the Montgomery County, MD area to support a well-established research organization focused on providing biopharmaceutical...
Suggested
Contract work
...expert functional advice as well as assistance to other functions as needed.
• Review, update, or write company SOPs related to Pharmacovigilance and safety reporting to ensure their compliance with EMA, ICH, and FDA guidelines.
• Assist in the preparation and review of...
Suggested
Local area
Remote job
...in a matrix environment) with colleagues in clinical development, program leadership, biometrics, clinical operations, safety/pharmacovigilance, regulatory, and translational research.
DUTIES AND RESPONSIBILITIES :
Responsible for ensuring the risk-benefit of a...
Suggested
Immediate start
Worldwide
...and Regional Operations.
+ Collaborates internally with HQ functions, regional and local operations, EU Clinical Development, Pharmacovigilence, Global Medical Affairs to align on key issues/decisions across the trials. Consult with GHH as needed.
**Extent of Travel:**...
Suggested
Holiday work
Local area
Remote job
Relocation
Visa sponsorship
Flexible hours
Shift work
3 days per week
...to the blinded Phase 3 clinical trial team.
Provide medical leadership for cross-functional internal workstreams including pharmacovigilance, biostatistics, clinical operations, and regulatory affairs.
Either directly monitor or provide medical safety oversight of...
Suggested
Holiday work
Flexible hours
...and Regional Operations.
+ Collaborates internally with HQ functions, regional and local operations, EU Clinical Development, Pharmacovigilance, Regulatory Affairs, Global Medical and Scientific Affairs to align on key issues/decisions across the trials. Consult with...
Suggested
Holiday work
Local area
Remote job
Relocation
Visa sponsorship
Flexible hours
Shift work
3 days per week
...services include clinical operations, project management, biostatistics, data management, regulatory affairs, medical affairs, and pharmacovigilance. ClinChoice has established major offices across US, China, Europe, India, Japan, and the Philippines with over 2,400...
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Remote job
...of drug product and biologics regulatory science, including: Chemistry, Manufacturing, and Controls (CMC); Clinical Research; Pharmacovigilance; Phase IV Research (e.g., Pharmacoepidemiology); and Drug and Biologics Discovery. Additionally, responsibilities include a Certificate...
Suggested
Full time
Remote job
Weekend work
...Senior Medical Director, Pharmacovigilance & Drug Safety
Boston, MA, USA Req #225
Friday, March 8, 2024
Who We Are:
Who We Are:
Xenon Pharmaceuticals (NASDAQ:XENE ) is a neuroscience-focused biopharmaceutical company committed to discovering...
Suggested
Temporary work
Local area
...Senior Medical Director, Drug Safety and Pharmacovigilance
Why Join Intellia?
Our mission is to develop curative genome editing treatments that can positively transform the lives of people living with severe and life-threatening diseases.
Beyond our science, we...
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Local area
...role in the design and oversight of clinical trials, in close partnership Clinical Strategy and Operations, Regulatory Affairs, Pharmacovigilence, and Clinical Research Organizations (CROs).
Key Responsibilities
Contribute to the elaboration of clinical development...
Suggested
Full time
Interim role
Local area
Remote job
...vaccines and therapeutics to benefit patients.
Here’s What You’ll Do:
Provide clinical and scientific leadership within the pharmacovigilance function.
Engage cross-functional internal workstreams including therapeutic area development, biostatistics, clinical...
Holiday work
Contract work
Flexible hours
...for the US that addresses current and future business needs, that is co-designed with Global Regulatory Sciences, Safety and Pharmacovigilance, Clinical Development and the Quality leadership and in partnership with our company’s policy teams at the global, regional and...
Holiday work
Flexible hours
...through the product lifecycle (e.g. surveillance, signal detection, validation and assessment). Interpreting regulations related to pharmacovigilance supporting all patient safety activities.
Responsibilities:
Understanding and application of the pharmacology, chemistry...
Holiday work
Temporary work
Local area
...’s What You’ll Do
Provide subject matter area expertise and leadership for cross-functional internal workstreams including Pharmacovigilance, Biostatistics, Clinical Operations, Regulatory Affairs and Brand teams.
Develop and foster relationships with external experts...
Holiday work
Full time
Second job
Local area
Flexible hours
...culture of our department and mentoring our junior staff. Your expertise will ensure our projects adhere to Good Clinical and Pharmacovigilance Practice and regulatory requirements. Are you up for the challenge?
When we put unexpected teams in the same room, we unleash...
Flexible hours
3 days per week
