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New · posted Oct 31

Alnylam Pharmaceuticals · Biotechnology

Senior Director, Clinical Research - Neurodegeneration

  • Cambridge, MA
  • Hybrid
  • Full-time
  • Director
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EmploymentFull-time
DeadlineOpen until filled

The role

Alnylam Pharmaceuticals is seeking an imaginative physician drug developer. This is an opportunity to provide clinical leadership in developing RNAi therapeutics in Alnylam’s rapidly expanding portfolio, which spans the areas of rare genetic diseases, cardio-metabolic diseases, neuroscience, hematology and hepatology.

The successful candidate’s primary role will be to drive the pipeline forward through leadership of clinical development programs.  While the primary focus responsibility will be as clinical lead physician on Alnylam’s Huntington’s program, the role may support across a range of therapeutic areas and all stages of development may be required as pipeline assets evolve. The Sr. Director is expected to play a leading and influencing role in the overall clinical development strategies and drive progress and operational excellence for associated clinical trials. In addition, this role will include interaction with Alnylam’s research group, helping to advise the team on the clinical development feasibility of novel targets and the design of proof-of-concept studies. This work will also involve extensive consultation and collaboration with external experts. It is expected that additional opportunities will arise to lead bench-to-bedside early phase clinical development programs.

The Senior Director, Clinical Research, will work in a matrix organization across Regulatory, Biostatistics, Clinical Operations, Preclinical, Commercial & QA teams to ensure fully harmonized and integrated development strategies. They will be a key Alnylam Development spokesperson at external meetings, including regulatory interactions and scientific meetings.

This position is hybrid and will be primarily located at our Cambridge, MA headquarters or Maidenhead, UK location.

What you need

  • MD with strong research background or MD PhD, with a track record of successful research support and peer review publications. Board Certification (or equivalent) or specialist training is highly desirable; drug development experience in neurology (Huntington’s Disease) would be a great advantage, but not essential
  • 10+ years industry experience or equivalent clinical academic experience
  • Sound scientific and clinical judgment
  • Successful track record of leading Phase 2/3 clinical programs (preferably in Huntington’s drug development), including major interactions with Health Authorities
  • Familiarity with concepts of clinical research and clinical trial design, including biostatistics, regulatory agency organization, guidelines, and practices
  • Ability to effectively present ideas and document complex medical/clinical concepts in both written and oral communication
  • History of solving problems while exhibiting superior judgment and a balanced, realistic understanding of issues
  • Outstanding leadership and collaboration skills working within a matrix environment.
  • Experience and knowledge of working with biotech/pharma partner(s) a plus
  • Thrives in highly entrepreneurial biotech environment and embraces Alnylam’s culture of science, passion and urgency.

About Alnylam: Alnylam Pharmaceuticals (Nasdaq: ALNY) has led the translation of RNA interference (RNAi) into a whole new class of innovative medicines with the potential to transform the lives of people afflicted with rare and more prevalent diseases. Based on Nobel Prize-winning science, RNAi therapeutics represent a powerful, clinically validated approach to treating diseases at their genetic source by “interfering” with mRNA that cause or contribute to disease. Since our founding in 2002, Alnylam has led the RNAi Revolution and continues to turn scientific possibility into reality.

Our culture: Our people-first culture is guided by our core values: fiercely innovative, open culture, purposeful urgency, passion for excellence, and commitment to people, and these values influence how we work and the business decisions we make. Thanks to feedback from our employees over the years, we’ve been fortunate to be named a top employer around the world. Alnylam is extremely proud to have been recognized as one of Science Magazine’s Top Biopharma Employers, one of America's Most Responsible Companies for 2024 by Newsweek, a Fast Company Best Workplace for Innovators, and a Great Place to Work in Canada, France, Italy, Spain, Switzerland, and UK – among others.

What you'll do

  • Be the strategic leader providing a strong, clear voice for the clinical programs
  • Develop creative but realistic approaches to drug development and lead clinical efforts to secure global regulatory approvals
  • Oversight of trial conduct and safety
  • Provide strategic consultation and guidance to Research on all decisions that have significant clinical components and implications.
  • Collaborate closely with Preclinical, Regulatory Affairs, Medical Affairs and Commercial to ensure tight strategic integration of product development plans
  • Be accountable via Clinical Research and Operations for all relevant timelines and deliverables
  • Drive/supervise all major written deliverables (regulatory submissions, original articles, abstracts), and presentation materials
  • Be responsible (as appropriate in line with SOPs) for final review and sign off with respect to all controlled documents including protocols, IBs, informed consent forms
  • Influence internal and external audiences in a high impact, highly visible fashion

Where you'll work

Cambridge, MAHybridOpen in Maps (opens in a new tab)

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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. We are dedicated to building an environment where employees can feel that they belong, can bring their authentic selves to work, and achieve to their full potential. By empowering employees to embrace their unique differences at work, our business grows stronger with advanced and original thinking, allowing us to bring groundbreaking medicines to patients.

Before applying, please review Alnylam's ⁠Candidate Privacy Notice regarding how Alnylam handles Personal Data you provide with your application for employment.

Job intelligence

The context around this role

Live data · October 31, 2026

Salary intelligence

How the pay compares

Director roles in Massachusetts40 roles publishing pay

Middle half $255,000 to $308,250, median $298,000

Director roles in the US93 roles publishing pay

Middle half $258,000 to $318,500, median $298,000
Annual base pay
Annual base payLowMedianHigh
Massachusetts$255,000$298,000$308,250
All US$258,000$298,000$318,500

Comparisons: the base pay employers published on open Clinical Development roles at the same level on Regulatory Jobs, October 31, 2026. Nothing is estimated.

Career trajectory

Where this role sits in Clinical Development

The general path across 116 open Clinical Development roles on Regulatory Jobs, with the titles they carry most. Not Alnylam's own promotion track.

  1. Earlier

    Associate & Specialist

    Often: Summer Intern

  2. Earlier

    Senior & Principal

    Often: Clinical Scientist · Clinical Scientist/Sr. Clinical Scientist, Oncology

  3. One step back

    Manager

    Often: Manager, Aesthetics Clinical Development · Senior Manager, Clinical Scientist

  4. This role

    Director

    Often: Senior Director, Clinical Development · Executive Medical Director, Oncology Clinical Development

    $298K median96 open
  5. Next step

    VP & Executive

    Often: Vice President, Clinical Development · Associate Vice President

    $360K median11 open

Skills DNA

What this role leans on

How many of the posting's 25 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.

Documentation and SOPs: 4 linesValidation and qualification: 1 lineRegulatory submissions: 3 linesClinical trial conduct: 5 linesCollaboration and leadership: 9 linesDocumentationValidationSubmissionsClinical trialsTeamwork
  • Collaboration and leadership9
  • Clinical trial conduct5
  • Documentation and SOPs4
  • Regulatory submissions3
  • Validation and qualification1

Company hiring pulse

Alnylam on Regulatory Jobs

15
Open roles
14
Distinct roles
4
Locations

By discipline

  • Clinical8 53%
  • Regulatory4 27%
  • Quality3 20%

By level

  • Director8 53%
  • Manager3 20%
  • Senior & Principal2 13%
See all 15 Alnylam roles

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Senior Director, Clinical Research - Neurodegeneration at Alnylam

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