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New · posted Nov 14

Alnylam Pharmaceuticals · Biotechnology

Executive 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 Executive 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 Executive 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, requiring weekly onsite presence and will be primarily located at our Cambridge, MA headquarters or Maidenhead, UK location. Relocation may be possible for the selected candidate.

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.

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

Pay and benefits

Alnylam Pharmaceuticals didn't publish pay for this role

See what similar roles pay on Regulatory Jobs, or try the salary calculator.

  • Relocation may be possible

Where you'll work

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

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Job intelligence

The context around this role

Live data · November 14, 2026

Salary intelligence

How the pay compares

Director roles in Massachusetts69 roles publishing pay

Middle half $235,500 to $320,000, median $297,000

Director roles in the US219 roles publishing pay

Middle half $253,000 to $335,500, median $300,000
Annual base pay
Annual base payLowMedianHigh
Massachusetts$235,500$297,000$320,000
All US$253,000$300,000$335,500

Comparisons: the base pay employers published on open Clinical Development roles at the same level on Regulatory Jobs, November 14, 2026. Nothing is estimated.

Career trajectory

Where this role sits in Clinical Development

The general path across 292 open Clinical Development roles on Regulatory Jobs, with the titles they carry most. Not Alnylam's own promotion track.

  1. Earlier

    Associate & Specialist

    Often: 2027 Summer Intern Clinical Science, Medical Monitoring & Health Economics · Clinical Research Scientist

    $80K median6 open
  2. Earlier

    Senior & Principal

    Often: Clinical Scientist · Senior Clinical Scientist

    $185K median25 open
  3. One step back

    Manager

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

    $199K median14 open
  4. This role

    Director

    Often: Senior Director, Clinical Development · Director, Clinical Development

    $300K median228 open
  5. Next step

    VP & Executive

    Often: Vice President, Clinical Development · Associate Vice President

    $400K median19 open

Skills DNA

What this role leans on

How many of the posting's 23 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.

Documentation and SOPs: 4 linesRegulatory submissions: 3 linesClinical trial conduct: 5 linesCollaboration and leadership: 9 linesDocumentationSubmissionsClinical trialsTeamwork
  • Collaboration and leadership9
  • Clinical trial conduct5
  • Documentation and SOPs4
  • Regulatory submissions3

Regulatory intelligence

The rules, regulations and standards behind this role

The regulations, guidance and standards that govern Clinical Development work in biotechnology, each linked to the agency or standards body that publishes it.

Company hiring pulse

Alnylam on Regulatory Jobs

19
Open roles
19
Distinct roles
5
Locations

By discipline

  • Clinical14 70%
  • Regulatory3 15%
  • Quality3 15%

By level

  • Director12 60%
  • Manager4 20%
  • Associate & Specialist2 10%
See all 19 Alnylam roles

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Executive Director, Clinical Research - Neurodegeneration at Alnylam

Open until filled.

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