or apply directly on Dyne Therapeutics's site. We never take the application ourselves.
Is this posting real?
- This role has been open
- 19 days Dyne Therapeutics's roles stay open a median of 45 days
- Reposted
- No
- Salary listed
- No 0% of Dyne Therapeutics's roles list one
- Ghost-job risk at Dyne Therapeutics
- high 58 stale, 1 reposted of 69 open
- Hiring momentum
- 88 roles opened in the last 90 days ↑ up vs. the prior 90 days
- Last confirmed on the employer's board
- 2026-09-17
Measured from postings appearing on and disappearing from Dyne Therapeutics's own greenhouse board since 2026-08-03. Full hiring picture for Dyne Therapeutics.
About this role
The Director, Clinical Scientist at Dyne Therapeutics will lead scientific and clinical development efforts for clinical studies targeting genetically driven neuromuscular diseases. This role involves collaborating with cross-functional teams to design and execute clinical trials, interpret data, and communicate findings effectively. The position requires strong expertise in clinical development and the ability to mentor others while maintaining a patient-focused approach.
- benefits
- 1/5
- freshness
- 4/5
- career value
- 4/5
- role clarity
- 5/5
- pay transparency
- 0/5
Scored from the posting itself — how clearly the role is described, how much it says about pay and benefits, and how recently it was listed. Not a judgement of Dyne Therapeutics as an employer.
What you need
- Advanced degree in life sciences, healthcare, pharmacy, medicine, nursing, or a clinically relevant discipline required
- 8+ years of relevant experience in clinical development, clinical science, clinical research, or related roles within the pharmaceutical or biotechnology industry
- Experience supporting or leading interventional clinical trials across multiple phases of development
- Demonstrated understanding of clinical development strategy, study design, protocol development, regulatory documentation, data review, clinical trial execution, and study reporting
- Strong knowledge and experience with GCP, ICH guidelines, FDA, EMA, and other applicable global regulatory requirements for clinical trials
- Excellent written, verbal, and presentation skills
Nice to have
- Experience in rare disease, neuromuscular disease, genetic medicines, oligonucleotide therapeutics, or other complex therapeutic areas
- Experience supporting global, late-stage clinical trials and submissions
- Experience developing or contributing to clinical and regulatory documents
- Experience working with CROs, investigators, study sites, key opinion leaders, advisory boards, or external experts
Worth weighing
- No specific mention of remote work options; position appears to be onsite
- 20% travel requirement for trial site visits and meetings
- Compensation range provided, but individual pay depends on various factors
- Role involves significant responsibility and influence without direct authority, which may require strong leadership skills
Summarised from Dyne Therapeutics's posting. Read the full original.
Listed by Dyne Therapeutics on their greenhouse job board, last confirmed open on 2026-09-17. PitchMeAI is not the employer.
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