Sr. Manager, Pharmacovigilance Operations - Remote
Full Time
Gaithersburg, MD 20879
Posted
Job description
We go where others won’t, taking on some of the biggest public health challenges to protect and enhance millions of lives, and create a better, more secure world. Here, you will join passionate professionals who advance their scientific, technical and professional skills to develop products designed-to protect and enhance life.JOB SUMMARY
The Sr Manager, Pharmacovigilance oversees the PV Operations team in the processing and submission of adverse event reports, as we as addressing medical inquiries. The Sr Manager, PV plays a key role in ensuring ongoing regulatory compliance.
ESSENTIAL FUNCTIONS
Reasonable accommodations will be made to enable individuals with disabilities to perform the essential functions.
- Manage daily operations of the Pharmacovigilance group, including receipt and processing of adverse events and medical inquiries
- Supervise the activities and development of Pharmacovigilance Specialists
- Develop and manage annual department budget
- Develop Safety Data Exchange Agreements with Contract Safety Organizations
- Oversee pharmacovigilance activities, including the entry of all adverse event data into the Argus database and the preparation of tracking and trending reports; preparation for monthly signal detection meetings
- Oversee compliance activities of the Pharmacovigilance group, including submission of 15-day reports and annual safety reports. Ensure that Pharmacovigilance activities and procedures and maintained in compliance with all U.S. regulations
- Serve as the Pharmacovigilance subject matter expert for internal audits and FDA inspections
- Serve as the main contact for the off-site database hosting company, which includes oversight of the Argus/MedDRA upgrades
- Work with the Head of Global Pharmacovigilance and EU QPPV to ensure global pharmacovigilance compliance
MINIMUM EDUCATION, EXPERIENCE, SKILLS
- Degree in medical or related science field. Advanced degree preferred.
- Ten or more years work experience in pharmaceutical industry; pharmacovigilance.
- Must understand medical terminology and medical coding using MedDRA
- Experience with Argus Safety or similar product database
- Basic understanding of epidemiology and statistics
- Strong oral and written communication skills
- Excellent analytical skills
There are physical/mental demands and work environment characteristics that must be met by an individual to successfully perform the essential functions of the job. This information is available upon request from the candidate.
Reasonable accommodations may be made to enable individuals with disabilities to perform all essential functions.
Emergent BioSolutions is an Equal Opportunity/Affirmative Action Employer and values the diversity of our workforce. Emergent does not discriminate on the basis of race, color, creed, religion, sex or gender (including pregnancy, childbirth, and related medical conditions), gender identity or gender expression (including transgender status), sexual orientation, age, national origin, ancestry, citizenship status, marital status, physical or mental disability, military service or veteran status, genetic information or any other characteristics protected by applicable federal, state or local law.
Information submitted will be used by Emergent BioSolutions for activities related to your prospective employment. Emergent BioSolutions respects your privacy and any use of the information submitted will be subject to the terms of our Privacy Policy .
Emergent BioSolutions does not accept non-solicited resumes or candidate submittals from search/recruiting agencies not already on Emergent BioSolutions’ approved agency list. Unsolicited resumes or candidate information submitted to Emergent BioSolutions by search/recruiting agencies not already on Emergent BioSolutions’ approved agency list shall become the property of Emergent BioSolutions and if the candidate is subsequently hired by Emergent BioSolutions, Emergent BioSolutions shall not owe any fee to the submitting agency.
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