Overview
On Site
$DOE
Accepts corp to corp applications
Contract - W2
Contract - Independent
Contract - 12+ Month(s)
Skills
Associate Director Safety Science
Safety Scientist
Signal Evaluation
Signal Management
Argus
Signal Detection"
Job Details
Hi,
Hope you are doing well.
My name is Rohen and I represent Vision InfoTech. Let me know if you're interested in the below position.
Role: Associate Director Safety Science
Location: Brisbane, CA (Hybrid so candidates need to be in nearby areas.)
Duration: 12+ months
Candidate must have active LinkedIn.
Must have Skills
- ICSR reviews in Argus safety database.
- Completed quarterly signal evaluation forms.
- Completed signal issue work-ups.
- Completed aggregate reports.
- Risk Management Plans.
- Slide decks for Safety Management Team/Product Safety Committee meetings.
Job Description:
The Associate Director Safety Science performs signal detection activities, prepares aggregate safety reports, reviews ICSRs, and works with cross-functional team to evaluate safety signals.
Scope
- Perform medical review of pre- and post-marketing individual case safety reports (ICSRs) and/or aggregate safety data involving BioMarin products to ensure accuracy of ICSR MedDRA coding, assessments of seriousness, expectedness, causality, and regulatory reporting.
- Assist in follow-up of important ICSRs to ensure relevant information is sought.
- Collaborate with Clinical Science, Medical Affairs, PV colleagues and applicable functional specialists to identify, evaluate and manage safety signals.
- Participate in the development development of safety surveillance and risk management plans for drug development programs.
- Contribute to the preparation of expedited and aggregate safety reports (e.g., 15-day Alert Report, SUSAR, PSUR (PBRER format), US PADER, Annual Safety Report, DSUR, IND Annual Report).
- Serve on Safety Management Team and liaise with clinical study/project teams, Clinical Operations, Medical Affairs, Biostatistics, Regulatory Affairs, Contract Research Organizations (CROs), Data Monitoring Committees and other entities as needed.
- Participate in the preparation and revision of company product labeling and RMP as appropriate.
- Assist with preparation and review safety section(s) of investigator brochures, protocols, informed consent forms, statistical analysis plans, clinical study reports, NDA/BLA/CTD submissions and other safety documents.
- Interface with business partners as needed in accordance with applicable safety Data Exchange Agreements.
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Rohen Singh
Talent Acquisition Specialist
VISION INFOTECH INC
Phone: .
Email:
368 Main Street, st#3, Melrose MA 02176
E-Verified Company
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