Senior Director, Head of PV Science

Alnylam Pharmaceuticals; Cambridge (MA); Hybrid; USD 245,500 - 332,100; Full time

Benefits offered by this job

Medical, dental, and vision coverage

Life and disability insurance

401(k) with company match

Paid time off and holidays

Flexible spending accounts

Job summary

Alnylam Pharmaceuticals in Cambridge (hybrid; on-site 2 days/week) seeks a Senior Director of PV Science and Aggregate Reports to lead the PV Science department and the Aggregate reports team, ensuring robust safety profiles across all product lifecycles.

You will partner with the Head of MSRM to drive risk management, signal detection, SOP development, and audits; oversee DSURs, PSURs and line listings; and coordinate with Regulatory Affairs, Medical Writing and Medical Affairs to deliver

Qualifications

• Master or doctorate in a medical/healthcare field or related discipline.
• Strong leadership and matrix collaboration experience.
• Extensive PV knowledge including regulatory requirements.
• Experience with safety operations and aggregate reports.

Responsibilities

• Lead PV Science department and Aggregate report specialists.
• Drive risk management system development and safety signal detection.
• Oversee DSURs, PSURs, and line listings; manage audits and inspections.
• Collaborate with SRM, Regulatory Affairs, Medical Writing, and Medical Affairs.

Skills

Leadership

Cross-functional collaboration

PV safety knowledge

Signal detection

Project management

Communication

Education

Master's or PhD in medical/healthcare

Tools

Argus Safety

Empirica

PV Analytics

Job description

Overview

Alnylam is the industry leader in the translation of RNA interference (RNAi) into a new class of innovative medicines with the potential to address the unmet needs of patients with debilitating diseases. Founded in 2002, Alnylam was built upon a bold vision of turning scientific possibility into reality and is now advancing a robust pipeline of investigational RNAi therapeutic medicines, including multiple programs in late-stage development.

The Senior Director of PV Science and Aggregate Reports is leading the PV Science department that includes all Alnylam PV Scientists and PV Fellows, and also the team of Aggregate reports specialists. In partnership with Head of Medical Safety and Risk Management (MSRM), the Senior Director will provide strategic leadership in development and management of safety profiles at all stages of the lifecycle for all Alnylam products, and will have accountability on Alnylam safety aggregate reports for submission to regulatory authorities, including, among others, Periodic Safety Update Reports, Developmental Safety Update Reports, and Risk Management Plans.

This is a hybrid role with on site presence required 2 days a week in either our Cambridge (preferred) or Philadelphia offices.

Summary of Key Responsibilities for PV Science

• Manage teams of PV Scientists and Fellows, as well as the Aggregate report specialists
• Responsible for operationalizing PV Science department to provide continuous support in development, implementation and maintenance of a risk management system for detection, assessment and minimization of risk for investigational and marketed products
• Work closely with the Head of MSRM and safety leads analyzing MSRM\'s team needs and potential process improvements in all functions, including routine and ad-hoc signaling activities, clinical trial initiations, regulatory interactions, and aggregate reports production
• Collaborate proactively with study teams, cross-functional team members, external business partners and vendors to apply knowledge and analytical skills to problem solving
• Implement and monitor process enhancements and improvements
• Manage participation of PV Scientists in Investigator meetings and Site Initiation meetings, ensuring effectiveness of the content delivery
• In partnership with Head of MSRM, provide scenario planning, strategy analysis, portfolio prioritisation, budget management and forecasting
• Responsible for ensuring the team can anticipate, develop and support improved/consistent scientific ways of working to implement effective Patient Safety and Risk Management processes. Lead development of relevant SOPs, work practices and training activities
• Participate in audits, inspections and quality improvement initiatives. Proactively manage process improvements and collaborate with Global Safety Operation team and other functions to address relevant corrective actions
• Oversee activities related to the functioning of Alnylam safety committees, including but not limited to, SRMT, SRMT Chairs and ESB meetings
• Provide direction on relevant meeting material preparation
• Ensure timely completion of all action items
• Participate in relevant safety discussions providing scientific and operational contributions
• Responsible for signal detection through global medical Literature monitoring
• Oversee creation of Development Risk Management Plans (DRMPs). Responsible for SME contributions to initial Risk Management Plans
• Lead the cross-functional collaboration between SRM, Regulatory Affairs, Medical Writing, Medical Affairs, and other functions for all activities related to regular updates of Risk Management Plans for approved products.

Summary of Key Responsibilities for Aggregate Safety Reports

• In agreement with the Head of SRM and the Head of MSRM, assess strategic options to ensure Alnylam readiness for aggregate reports production, including insourcing vs outsourcing, AI capabilities build, geographical footprint
• Oversee planning, production and successful submission of DSURs for all Alnylam products in development. In collaboration with required stakeholders, responsible for Health Authorities\' communications in relation to DSURs
• Responsible for planning, production, and successful submission of PSURs. In close collaboration with safety physicians and other contributing functions, oversee the authoring of the report, including strategy of the safety analysis. In collaboration with required stakeholders, responsible for Health Authorities\' communications in relation to PSURs.
• Oversee production of Line Listings and their appropriate and timely submissions to required authorities
• Serve as an SME for Aggregate Reports during inspections and audits

Qualifications

Education: Master or doctorate degree in a medical or healthcare related discipline (MD, PharmD, RN), or relevant scientific discipline.

Experience: A minimum of 12 years in the pharmaceutical industry with a minimum of 8 years in drug safety/pharmacovigilance. A minimum of 5 years of experience in managing teams. Specific experience in RNAi therapeutics and rare disease areas at a global level is an advantage

Required skills and experience:

• Strong leadership and team building skills with track record of team building and expansion
• Extensive knowledge of Pharmacovigilance and advanced knowledge of Global (including US, EU, LATAM, APAC) Pharmacovigilance regulatory requirements including device safety regulations
• Extensive knowledge of safety operations, including but not limited to case processing and aggregate reports production
• Ability to work in a matrix environment in accordance with the company leadership commitments and values. Experience of working across diverse geographic areas, business settings and cultures strongly preferred
• Ability to apply business process improvement methodologies and/or developing ideas into practical business solutions
• Extensive knowledge of Argus Safety Database and Signaling tools (eg. Empirica, PV Analytics)
• Regulatory Inspection readiness experience
• Strong planning, organization, and budgeting skills
• Superb written and oral communication skills
• Adaptability and ability to approach change with positivity and foster a resilient environment
• Ability to foster collaboration within internal and external teams maintaining supportive and positive work culture

Special Skills: Ability to represent the functional department as primary internal and external contact for services relating to PV Science department. Lead cross-functional briefings and technical meetings for project stakeholders and customer representatives. Strong negotiation skills and ability to encourage discussion and drive decisions to desired results. Strong analytic and scientific data interpretation skills.

Supervision: Individual is expected to work independently with support from management and colleagues in SRM.

#LI-JB1 #LI-Hybrid

U.S. Pay Range

$245,500.00 - $332,100.00

The pay range 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).

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

About Alnylam

We are the leader in RNAi therapeutics- a revolutionaryapproach 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 possibleand 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, wherean authentic, inclusive culture and breakthrough thinkingfuel one another.

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.