Senior Manager, Global Pharmacovigilance Operations
San Francisco, United States
Job Description
Vir Biotechnology is looking for a Senior Manager, Pharmacovigilance Operations Contractor to help support the global PV Operations team.
This role is located in San Francisco and will report to the Director of PVRM Operations.
RESPONSIBILITIES AND LEARNING OPPORTUNITIES:
- Support the daily functioning of the Pharmacovigilance Operations Department.
- Assist with compliance with standard operating procedures (SOPs), regulatory safety, and pharmacovigilance in compliance with US and global regulations.
- Responsible for operational tasks related to electronic Trial Master File documents, including quality review, organization, maintenance, and storage following study procedures.
- Help with Pharmacovigilance mailbox (i.e. ensure all emails are processed, identify requests, ensure all emails are prioritized and organized as well as follow-up on outstanding deliverables).
- Perform quality review of individual case safety reports (ICSR)
- Help track submissions of ICSRs and aggregate safety reports (i.e. line listings, DSURs, PADERs, PSURs/PBRERs, IND Annual Reports, PADERs, etc.).
- Communicate with pharmacovigilance and clinical vendors for all pharmacovigilance operations activities.
- Participate in set-up of new clinical trials, including development of study-specific Safety Management Plans and Forms.
- Assist in writing and maintenance of Global PVRM and safety related cross functional SOPs and work instructions
- Manage review of Safety Regulatory Intelligence within Global PVRM
- Help with other activities and special projects
QUALIFICATIONS AND EXPERIENCE:
- RN/PharmD or similar degree with 5+ years of experience in drug safety/pharmacovigilance operations with broad exposure to Trial Master File (TMF) and ICSR activities.
- Working knowledge of domestic and international adverse event reporting regulations (ICH, EMA GPV, GCP, FDA etc.)
- Experience in case management and case processing activities.
- Experience using ARGUS or other safety databases.
- Experience with MedDRA/WHODrug for coding AEs, medical history, and concomitant medications.
- Experience writing SOPs
- This role is located in San Francisco at our corporate office and there is a requirement to be onsite at least three days per week.
The expected salary range for this position is $55.00 to 78.00/Hour. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors.
#LI-Onsite
Vir Biotechnology (“Vir”) is an equal opportunity employer. All employment decisions at Vir are based on legitimate, non-discriminatory business requirements, job duties and individual qualifications. Employment decisions are made without regard to race, color, religion, sex (including pregnancy), gender, gender identity, gender expression, sexual orientation, age, parental status, marital status, national origin, ancestry, disability, medical condition, genetic information (including family medical history), political affiliation, military service or any other legally protected characteristic.
This commitment extends to all management practices and decisions, including recruitment and hiring, compensation, appraisal systems, promotions, training and career development programs. Vir also strongly commits to providing employees with a work environment free of unlawful discrimination or harassment.
Apply
Career Focus: Analyst, Drug Safety/Pharmacovigilance, Regulatory/Compliance
Similar Jobs
Senior Director, Clinical Development –...
This individual will be directly, and through the team, responsible for ...
Senior Director, Clinical Development –...
This individual will be directly, and through the team, responsible for ...
Associate Director, Drug Product and...
We were born of innovation, springing from the curiosity, imagination an...
Senior Scientist, Computational Biology
The Computational Biologist will work closely with scientists and other ...