Associate Director Pharmacovigilance Quality Assurance
Associate Director Pharmacovigilance Quality Assurance
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$ 156000 - 195000
1 Vacancy
Job Description
Why Sarepta Why Now
The promise of genetic medicine has arrived and Sarepta is at the forefront. We hold leadership positions in Duchenne muscular dystrophy (DMD) and limbgirdle muscular dystrophies (LGMDs) and we currently have more than 40 programs in various stages of development in gene therapy RNA and gene editing. In 2023 we launched our fourth therapy and the first ever gene therapy to treat Duchenne.
Were looking for people who see unlimited potential in themselves and who are motivated by an unwavering commitment to patients.
What Sarepta Offers
At Sarepta we care deeply about all the people in our community and believe in the importance of supporting them in all aspects of their lives. We aspire to maintain a culture that acknowledges people bring their whole selves to work and we will strive to help everyone in our community integrate their work and personal lives while maintaining productivity. We are committed to offering a range of benefits and worklife resources designed to support people in the following areas:
Physical and Emotional Wellness
Financial Wellness
Support for Caregivers
For a full list of our comprehensive benefits see our website: Importance of the Role
The Associate Director R&CD QA Pharmacovigilance with minimal supervision will support the management of GVP quality oversight GVPrelated audit program and for providing regulatory/GVP guidance. This position will liaise with internal groups such as Pharmacovigilance Operations Safety Evaluation & Risk Management and Market Research as well as external groups including contract auditors in an effort to ensure a high level of quality and consistency across the Sarepta platform; design and oversee the audit strategy; assist the GVP team in identifying and implementing corrective and preventive actions; and enable teams to be inspection ready in support of a culture of sustainable compliance.This position will participate in inspection readiness activities and audits as appropriate. This position will have direct reports and report to the Director Research & Clinical Development Quality Assurance (R&CD QA).
The Opportunity to Make a Difference
Participate in the development of the internal and external R&CD QA annual audit plan for GVP REMS PV vendors interfaces processes and preferred business partners and update the audit plan as needed based on identified risks and priorities
Provide oversight and support to global Pharmacovigilance (PV) function to identify risks and risk mitigation strategies
Support the existing longterm audit strategy for GVPrelated audits to meet applicable regulatory requirements.
Support the timely development and distribution of audit reports and follow up actions
Collaborate with key stakeholders to ensure audit plan .
Ensure the corrective and preventive actions are appropriately identified and completed in a timely manner.
Assist in the review and identification of potential systemic gaps and coordinate with the appropriate stakeholder to ensure timely remediation.
As appropriate escalate issues of critical noncompliance and/or lack of urgency in remediation to senior management.
Work collaboratively to perform investigations to identify root cause of compliance issues and provide appropriate metrics for tracking trending for the overall reporting requirements to functional and senior management.
Develop and/or review SOPs Policies documents etc. as needed
Serve in an advisory/consultative role in compliance related matters for pharmacovigilance and support the internal team in evaluating metrics and trending exercises and/or identifying implementing corrective and preventive actions.
Participate in inspection readiness and preparedness activities and support regulatory inspections
More about You
as above
What Now
Were always looking for solutionoriented critical thinkers.
So if youre comfortable with ambiguity and candor relish challenging yourself and place kindness and integrity at the forefront of how you approach your peers and work then we encourage you to apply.
Required Experience:
Director
Employment Type
Full-Time
