New · posted Oct 31
Celldex Therapeutics · Biotechnology
Vice President, Pharmacovigilance & Risk Management
- Hampton, NJ
- On-site
- Full-time
- VP & Executive
The role
Celldex is pioneering new horizons in immunology to deliver life-changing therapies. We are relentless in our pursuit of novel antibody-based treatments that engage the human immune system and directly impact critical pathways in allergic, inflammatory, and autoimmune diseases.
As we advance toward potential commercialization of our lead asset, barzolvolimab, and continue to expand our late-stage pipeline, we are building a world-class organization capable of supporting both development and future commercial readiness. Our entrepreneurial culture empowers leaders to build, innovate, and drive meaningful impact for patients.
The Vice President, Pharmacovigilance & Risk Management will provide strategic and operational leadership for Celldex’s global pharmacovigilance and risk management function across the product lifecycle, from clinical development through commercialization.
Reporting to the SVP, Chief Medical Officer, this individual will serve as the company’s senior safety leader, responsible for the oversight, evolution, and execution of all pharmacovigilance activities, ensuring compliance with global regulatory requirements while proactively identifying, evaluating, and managing product safety risks.
This leader will play a critical role in shaping Celldex’s safety strategy in support of late-stage development, regulatory submissions, and launch preparation.
What you need
Education
- MD required, specialty and or experience managing drug safety
- 15+ years of experience within the pharmaceutical/biotechnology industry, including significant leadership experience in Pharmacovigilance and Drug Safety
- Deep expertise in global pharmacovigilance regulations, safety surveillance, and risk management across clinical development and post-marketing environments
- Experience supporting late-stage development programs, regulatory submissions, and/or product launches
- Proven ability to lead and scale pharmacovigilance organizations within a growing biotech or pharmaceutical company
- Strong scientific and clinical acumen with the ability to synthesize and communicate complex safety information
- Demonstrated success working cross-functionally and influencing within matrixed organizations
- Excellent leadership, communication, and stakeholder management skills
- Ability to thrive in a fast-paced, entrepreneurial environment
Preferred Skillsnice to have
- Experience in Immunology, Allergy, Dermatology, or related therapeutic areas preferred
- Experience supporting global development programs and commercialization readiness
- Experience with safety systems implementation and pharmacovigilance operational scaling in emerging biotech environments
What you'll do
Strategic Pharmacovigilance Leadership
- Provide overall strategic leadership and direction for the global Pharmacovigilance and Risk Management function
- Develop and execute the company’s global safety strategy across clinical and future commercial programs
- Lead the continued evolution of pharmacovigilance infrastructure, systems, processes, and governance to support organizational growth and commercialization readiness
- Serve as the senior safety advisor to executive leadership and cross-functional teams
Safety Surveillance & Risk Management
- Ensure oversight and execution of all safety surveillance activities, including:
- Individual case safety report (ICSR) processing and medical review
- Signal detection and management
- Aggregate safety analysis and reporting
- Benefit-risk assessments
- Risk management planning and mitigation strategies
- Oversee preparation and review of safety-related regulatory submissions and responses to global health authorities
- Ensure timely identification, evaluation, escalation, and communication of safety risks across programs
Regulatory & Compliance Oversight
- Maintain deep expertise in global pharmacovigilance regulations, guidance, and industry best practices
- Ensure compliance with FDA, EMA, ICH, and other applicable global safety reporting requirements
- Lead inspection readiness and support regulatory inspections and audits related to pharmacovigilance
Cross-Functional Leadership
- Partner closely with Clinical Development, Clinical Operations, Regulatory Affairs, Biostatistics, Medical Affairs, Quality, and Commercial organizations on safety-related strategy and execution
- Contribute to development programs, regulatory submissions, labeling discussions, and launch planning activities
- Support Safety Governance Committees and cross-functional safety review forums
Organizational & Operational Excellence
- Lead departmental operations including organizational design, resourcing, vendor oversight, SOPs, training, technology, and budget management
- Recruit, develop, and retain high-performing pharmacovigilance talent
- Foster a collaborative, patient-focused, and scientifically rigorous culture within the safety organization
- Drive operational excellence and continuous process improvement across the function
Pay and benefits
$308,977 – $401,269 a year
Employer providedThe expected base salary range for this position is $308,977-$401,269.
We are committed to compensating employees equitably based on several factors including experience, education, licensure/certifications, skill level, location of the position, and availability of similar talent in a competitive market.
Compensation for this role includes base salary, annual discretionary bonus, long term incentive, 401(K) plan with employer contribution, health care and other insurance benefits (for employee and family), paid holidays, vacation, and sick days. A summary of our benefits can be found on our careers page.
Annual discretionary bonus
Long-term incentive
401(k) with employer contribution
Health care and other insurance benefits
Paid holidays
Vacation and sick days
Where you'll work
Hampton, NJOn-siteOpen in Maps (opens in a new tab)
More jobs in Hampton, NJ
From the posting
About Celldex Therapeutics
About Celldex
Celldex is pioneering new horizons in immunology to deliver life-changing therapies. We are relentless in our pursuit of novel antibody-based treatments that engage the human immune system and directly affect critical pathways to improve the lives of patients with allergic, inflammatory and autoimmune disorders. We have built a culture where innovative and talented people thrive—focusing a significant effort on attracting and retaining passionate and motivated employees who want to play a role in helping people with serious health conditions and who see this effort as personally rewarding. In our highly entrepreneurial environment, employees are empowered and the opportunity for professional development occurs every day.
Equal opportunity, accessibility and legal noticesCelldex Therapeutics's statements, word for word
Celldex is proud to be an equal opportunity employer that strives to foster a culture of diversity, equity, and inclusion. We are committed to promoting a diverse environment through development, recruiting and community outreach.
Job intelligence
The context around this role
Live data · October 31, 2026
Salary intelligence
How the pay compares
This role's midpoint is 2% above the US median for Clinical Safety & Pharmacovigilance roles at this level.
This roleEmployer provided
VP & Executive roles in the US10 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| This role | $308,977 | — | $401,269 |
| All US (middle half) | $346,500 | $346,500 | $353,125 |
This role: Celldex Therapeutics's own published range. Comparisons: the base pay employers published on open Clinical Safety & Pharmacovigilance roles at the same level on Regulatory Jobs, October 31, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Clinical Safety & Pharmacovigilance
The general path across 113 open Clinical Safety & Pharmacovigilance roles on Regulatory Jobs, with the titles they carry most. Not Celldex Therapeutics's own promotion track.
Skills DNA
What this role leans on
How many of the posting's 39 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- Collaboration and leadership17
- Quality systems and risk6
- GMP and compliance5
- Regulatory submissions4
- Clinical trial conduct4
- Documentation and SOPs2
Regulatory intelligence
The rules behind this role
Frameworks and standards this posting's work falls under, matched from its own words, each linked to the official source.
Company hiring pulse
Celldex Therapeutics on Regulatory Jobs
- 8
- Open roles
- 8
- Distinct roles
- 3
- Locations
By discipline
- Quality5 63%
- Clinical3 38%
By level
- Director3 38%
- Associate & Specialist2 25%
- VP & Executive1 13%
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Vice President, Pharmacovigilance & Risk Management at Celldex Therapeutics
Applications close June 9. $309K–$401K a year, employer provided.