Vice President, Pharmacovigilance
This is the employer's own posting, not a copy on a job board.
What we know
Is it still open?
Confirmed still open
Last checked 15h ago — checked against the employer's own applicant tracking system, which is the company answering directly.
We re-read the employer's own applicant tracking system and the posting was still there. That is the company answering directly.
How old is it?
Posted 45d ago
The date the source published, not the day we noticed it (2026-08-27). Last seen at its source 1h ago.
We have tracked this listing since 5 Oct 2026 (6 days). The employer's own board has carried it every time we have read it, most recently 1 hour ago.
Is it remote?
Remote - US
That is the location the employer filed this posting under. Quoted as written — we do not re-word the source's own location.
Who may apply?
United States
The description states no restriction of its own. This is the source's own tag.
Skills named in the ad
Recognised terms only, from a fixed vocabulary — this is what CV matching compares against.
Carried by 1 source
-
Ashby employer's own board first seen 6d ago · last seen 1h ago
The listing
Summary
We are seeking an accomplished Vice President of Global Drug Safety & Pharmacovigilance is an experienced healthcare professional (HCP) with expertise in good pharmacovigilance practices and international regulatory requirements (EMA/FDA/ICH). As the leader of the function, this individual is responsible for establishing and overseeing pharmacovigilance strategy & operations to ensure the safety of patients receiving company products.
Responsibilities
Develop and implement pharmacovigilance processes, policies, SOPs, and safety database/PV systems.
Lead cross-functional governance, benefit-risk assessment, signal detection, and risk management efforts.
Chair the executive safety review committee, oversee safety data exchange with partners, and contribute to industry-wide safety initiatives.
Partner with clinical development to integrate safety into protocols, risk management plans, and safety charters.
Provide PV oversight for regulatory filings (IND/BLA/MAA) - including Clinical Overviews, ISS, and RMPs - and review IBs, DSURs, and key CSR sections; participate in regulatory meetings as needed.
Lead medical review of ICSRs and oversee PV team operations, quality, and compliance with global safety regulations.
Monitor and assess CRO performance on pharmacovigilance activities.
Recruit, hire, train, mentor, and coach PV staff, and oversee project deliverables and performance evaluations.
Qualifications & Education
MD, with clinical and industry experience and a proven track record leading pharmacovigilance teams.
Minimum of 15 years' experience in drug safety and pharmacovigilance roles in the biotech or pharmaceutical industry.
Proven leadership expertise, including a track record of building and leading high-performing teams.
In-depth knowledge of global pharmacovigilance regulations and compliance requirements (EMA/FDA/ICH).
Strong leadership and strategic decision-making abilities to drive safety initiatives and ensure regulatory compliance.
Immunic Therapeutics is an Equal Opportunity Employer. We are committed to fostering a diverse, inclusive, and equitable workplace where all individuals are valued and respected. Employment decisions are based on qualifications, merit, and business needs, without regard to race, color, religion, gender, sexual orientation, national origin, disability, veteran status, or any other protected status.
Please note, Immunic does not accept unsolicited resumes from external agencies or recruiters. Submission of a resume without a prior written agreement does not create any express or implied contract between Immunic and the agency. Immunic will not pay any fees related to unsolicited resumes.