New · posted Oct 15
Alnylam Pharmaceuticals · Biotechnology
Senior Director, Global Pharmacovigilance Quality Assurance Lead
- Cambridge, MA +2 more
- Hybrid
- Full-time
- Director
Open until filled
The role
The Senior Director, Global Pharmacovigilance Quality Assurance Lead provides executive leadership and independent quality oversight of Alnylam’s global pharmacovigilance quality system. Reporting to the Vice President, R&D Quality, the role sets the strategic direction for the GVP QA function and provides independent assurance and escalation regarding the effectiveness of PV procedures, systems, and governance. As Alnylam continues to expand its global portfolio and organizational complexity, the Senior Director will lead the continued evolution of the PV Quality Assurance function, strengthening independent oversight, governance, risk-based assurance, quality-system performance monitoring, and inspection-readiness capabilities to support sustainable growth, operational excellence, and long-term regulatory compliance.
This role can be based in Cambridge, MA or Philadelphia, PA in a hybrid work arrangement, or remotely within the United States.
The pay range below reflects the full-time base salary range we expect to pay for this role at the time of posting. Base pay will be determined based on a number of factors including, but not limited to, relevant experience, skills, and education. This role is eligible for an annual short-term incentive award (e.g., bonus or sales incentive) and an annual long-term incentive award (e.g., equity).
What you need
- Bachelor’s degree in a scientific, healthcare, or related discipline; advanced degree such as MSc, PharmD, or PhD preferred.
- 12-15+ years of experience in pharmacovigilance quality assurance, regulated pharmacovigilance, or a related quality/compliance function, including substantial leadership experience.
- Thorough knowledge of international GVP regulations and guidance, including FDA requirements, EMA GVP Modules, Health Canada requirements, and applicable ICH guidance; working knowledge of GCP interfaces is expected.
- Demonstrated success strengthening, scaling, or transforming an independent PV Quality Assurance function, operating model, governance framework, risk-based assurance program, audit strategy, quality metrics, and continuous-improvement capabilities in a matrixed environment.
- Proven experience with risk-based GVP audits and health-authority inspections, including QPPV and PSMF-related scope.
- Executive presence and demonstrated ability to align operational, embedded compliance, and independent Quality Assurance stakeholders while preserving clear decision rights and escalation authority.
- Excellent problem-solving, decision-making, negotiation, communication, and conflict-resolution skills.
Skills named in this posting
What you'll do
- Provides strategic leadership for Alnylam’s global Pharmacovigilance (PV) Quality Assurance function, including long-term strategy, operating model, organizational design, talent development, and quality culture grounded in integrity, transparency, and continuous improvement.
- Leads and evolves the PV QA governance framework, overseeing compliance risk management, quality metrics, trend analysis, management reviews, and escalation of significant quality and regulatory risks.
- Serves as the independent QA authority for the pharmacovigilance quality system, providing oversight of quality events, CAPAs, compliance assessments, and remediation activities to ensure regulatory compliance and effectiveness.
- Owns the risk-based GVP audit strategy and PV assurance program. Partners with enterprise audit operations to conduct robust, risk-based audits of internal processes, vendors, and delegated partners while driving continuous improvement and risk mitigation across the PV ecosystem.
- Provides independent assurance over computerized systems supporting pharmacovigilance, including validation, data integrity, and change control, and oversees GVP QA contributions to the Pharmacovigilance System Master File (PSMF).
- Leads PV Quality Assurance inspection readiness in partnership with key enterprise stakeholders. Serves as a key representative during global health authority inspections, ensuring effective preparation, response management, and remediation oversight, including independent review of responses and remediation actions.
- Partners broadly across Safety, Quality, Regulatory, Clinical, Commercial, and enterprise functions to enable compliant execution, strengthen governance, align quality processes, and maintain independent QA decision-making and escalation authority.
Pay and benefits
$227,900 – $308,300 a year
Employer providedMedical, dental, and vision coverage
Life and disability insurance
401(k) with company match
Paid time off, wellness days, and holidays
Annual bonus and equity incentive eligibility
Family resources and leave
Where you'll work
Cambridge, MA +2 moreHybridOpen in Maps (opens in a new tab)
Also posted for: Philadelphia, PA · Remote (US)
More jobs in Cambridge, MA +2 more
From the posting
About Alnylam
We are the leader in RNAi therapeutics – a revolutionary approach with the potential to transform the lives of people with rare and common diseases. Built on Nobel Prize-winning science, Alnylam has delivered the breakthroughs that made RNAi therapeutics possible and are just at the beginning of what’s possible. Our deep pipeline, late-stage programs, and bold vision reflect our core values: fierce innovation, passion for excellence, purposeful urgency, open culture and commitment to people. We're proud to be a globally recognized top employer, where an authentic, inclusive culture and breakthrough thinking fuel one another.
Alnylam’s robust Total Rewards package is designed to support your overall health and well-being. We offer comprehensive benefits including medical, dental, and vision coverage, life and disability insurance, a lifestyle reimbursement program, flexible spending and health savings accounts and a 401(k)with a generous company match. Eligible employees enjoy paid time off, wellness days, holidays, and two company-wide recharge breaks. We also offer generous family resources and leave. Our commitment to your well-being reflects our belief that caring for our people fuels the impact we create together.
Learn more about these and additional benefits offered by Alnylam by visiting the Benefits section of the Careers website: https://www.alnylam.com/careers
U.S. Pay Range
$227,900—$308,300 USD
Equal opportunity, accessibility and legal noticesAlnylam Pharmaceuticals's statements, word for word
At Alnylam, we commit to an inclusive recruitment process and equal employment opportunity. Qualified applicants will receive consideration for employment without regard to their sex, gender or gender identity, sexual orientation, race, color, ethnicity, national origin, ancestry, citizenship, religion, creed, physical or mental disability, pregnancy status or related conditions, genetic information, veteran or military status, marital or familial status, political affiliation, age, or any other factor protected by federal, state, or local law. Alnylam is an E-Verify Employer.
Before applying, please review Alnylam's Candidate Privacy Notice regarding how Alnylam handles Personal Data you provide with your application for employment.#LI-LJ1
Job intelligence
The context around this role
Live data · October 15, 2026
Salary intelligence
How the pay compares
This role's midpoint is 18% above the US median for Clinical Quality & Safety roles at this level.
This roleEmployer provided
Director roles in Massachusetts10 roles publishing pay
Director roles in the US19 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| This role | $227,900 | — | $308,300 |
| Massachusetts (middle half) | $199,125 | $227,500 | $229,500 |
| All US (middle half) | $205,500 | $228,000 | $253,500 |
This role: Alnylam Pharmaceuticals's own published range. Comparisons: the base pay employers published on open Clinical Quality & Safety roles at the same level on Regulatory Jobs, October 15, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Clinical Quality & Safety
The general path across 34 open Clinical Quality & Safety roles on Regulatory Jobs, with the titles they carry most. Not Alnylam's own promotion track.
Skills DNA
What this role leans on
How many of the posting's 17 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- GMP and compliance10
- Quality systems and risk7
- Collaboration and leadership7
- Documentation and SOPs1
- Validation and qualification1
- Regulatory submissions1
- Data and digital systems1
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.
- FDAFDA data integrity guidance(official source, opens in a new tab)Data Integrity and Compliance With Drug CGMP: Questions and Answers
- ICHICH quality guidelines(official source, opens in a new tab)Q1 stability, Q2(R2) analytical validation, Q7, Q9 risk management, Q10 quality systems
- ICHICH E6 good clinical practice(official source, opens in a new tab)The international standard for the conduct of clinical trials
Company hiring pulse
Alnylam on Regulatory Jobs
- 7
- Open roles
- 7
- Distinct roles
- 3
- Locations
By discipline
- Regulatory3 43%
- Quality2 29%
- Compliance & Safety2 29%
By level
- Director4 57%
- Manager1 14%
- Senior & Principal1 14%
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Senior Director, Global Pharmacovigilance Quality Assurance Lead at Alnylam
Open until filled. $228K–$308K a year, employer provided.