Beeline Medicines

Pharmacovigilance Medical Director

United States · Director

Sponsorship not specified$266k-$344kDetected 20 days ago

Clinical TrialsFDA RegulatoryPharmacovigilanceLeadershipCollaborationMentoringPublic SpeakingRegulatory Affairs

About the role

This role serves as the primary physician voice for benefit-risk evaluation, signal assessment, and safety governance, ensuring that patient safety is upheld as the foundational principle of all clinical development and post-market activities.
Remote - This position is designated as remote
The frequency and scheduling of such visits will be determined at the company's discretion based on business need.

Perform other duties and responsibilities as assigned
the incumbent will be expected to travel to Beeline Medicines' offices on a periodic basis to support in-person collaboration, team engagement, and business operations.

Deep knowledge of global safety and pharmacovigilance regulations including FDA guidance, EU GVP Modules I-XVI and ICH guidelines
Experience contributing to Risk Management Plans (RMPs) and REMS programs, including development of risk minimization measures and assessment of effectiveness.

board certification or eligibility in immunology, rheumatology, internal medicine, or a relevant specialty experience in autoimmune disease is strongly preferred
Minimum of 5 years of combined clinical and pharmaceutical/biotech industry experience, with at least 2-3 years of dedicated pharmacovigilance or drug safety experience preferred.

The expected salary range for this position varies by location and will be communicated based on the country or region in which the selected candidate is hired.
Actual pay will be determined based on experience, qualifications, location, and other job-related factors permitted by applicable local law.
A discretionary annual bonus and long-term incentive award (e.g., equity) may be available based on individual and Company performance.
$266,000 - $344,000 USD
Equal Employment Opportunity:
We celebrate diversity and are committed to creating an inclusive environment for all employees.

We offer a comprehensive benefits package tailored to the country and region in which you are hired, in compliance with local laws and practices.
Competitive health and wellness coverage (structure and premiums vary by country)
Paid time off, public holidays, and additional leave entitlements in accordance with local requirements
Specific benefit details applicable to your country or region will be provided during the offer process.
Benefits may include, but are not limited to:
Flexible work arrangements / hybrid schedule
Benefits vary by location and are subject to eligibility requirements, local regulations, and plan terms.

Beeline Medicines is a clinical‑stage biotechnology company focused on developing and delivering category-leading precision therapies to transform the lives of people living with autoimmune and inflammatory diseases.
With a portfolio of potential best-in-class and first-in-disease therapeutic candidates that directly target key pathways governing dysregulated immunological and inflammatory responses, the Company is developing medicines that have the opportunity to provide durable, life-changing impact.
Led by an established executive team and backed by world-class life science investors, each day Beeline Medicines is determined to bring the scientific rigor and operational excellence to get to what matters for patients - realizing a world where people with immune-mediated diseases can live life fully.
Lead the discussion at the company's Safety surveillance governance, providing medical and strategic direction on safety signal management, escalation procedures, and corrective action planning.

If you require a reasonable accommodation to participate in the application or interview process, please contact careers@beelinemedicines.com to request an accommodation.
We are committed to providing equal access to all candidates.
Beeline Medicines is an Equal Opportunity Employer.
We celebrate diversity and are committed to creating an inclusive environment for all employees.

d or participate in DSMB oversight, clinical trial safety monitoring, and safety governance committee activities at the sponsor level

This listing is sourced directly from Beeline Medicines's careers page and normalized into a canonical job model.