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Boehringer Ingelheim Vetmedica.Inc.
Manager, Pharmacovigilance
Job Location: Saint Joseph, MO
Department:
R&D / Science/Research & Development
Shift:
Full Time
Our Culture - Come Discover Us
In a world where business is driven by short term financial goals, Boehringer Ingelheim Corporation is truly a company with a different philosophy. Although we are one of the largest and fastest growing pharmaceutical companies in the world, we have been able to maintain a dedication to our values. Our focus is on helping patients, serving our customers and improving the quality of life for the millions of people who rely on us. Simply put, we have remained committed to doing the right thing-for our customers, our communities, our employees and everyone we serve. At Boehringer Ingelheim, we realize that our strength and competitive advantage lie with our people. We support our employees in a number of ways to create a healthy working environment-meaningful work, diversity, mobility, networking and work-life balance. Boehringer Ingelheim is firmly committed to ensuring a safe, healthy, productive and efficient work environment for our employees, as well as our partners and customers. As part of that commitment, Boehringer Ingelheim conducts pre-employment background checks and drug screenings.
Job Description
QUALIFICATIONS:
- Must be a Doctor of Veterinary Medicine
- Minimum of 8 – 10 years of previous experience in animal health care
- Must have a strong interest and capability in managing a pharmacovigilance program in a call center/post-market surveillance environment
- Must have thorough veterinary knowledge of infectious diseases/conditions afflicting both large and companion animals
- Sound knowledge of veterinary drug development process and global regulatory requirements preferred
- Working knowledge of GCP, FDA, and European regulations regarding drug safety reporting requirements is desirable
- Must have outstanding verbal and written communication skills and be computer literate
DUTIES & RESPONSIBILITIES:
- Assure a timely review and response to incoming Suspected Adverse Drug Event reports received from clinical trials and from post-marketing surveillance
- Manage the day-to-day pharmacovigilance program to assure compliance with corporate procedures and with US and other global government regulations in the event of an audit/inspection
- Co-ordinate ongoing safety surveillance for signals or trends and set up/lead Safety Review Committees on company products
- Lecture and train on pharmacovigilance procedures at investigator meetings, sales staff training sessions, medical science liaison training sessions, SOP meetings, and other meetings as needed
- Supervise, manage, and mentor pharmacovigilance staff (e.g. veterinarians, specialist, administrative assistants)
- Represent pharmacovigilance group at meetings with corporate partners or CROs as needed to ensure safety surveillance obligations continue to be met
Click Here To Apply
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