Director, Regulatory Writing
Entrada Therapeutics · Boston, MA
Posted 15 days ago · $220,000 - $249,711
or apply directly on Entrada Therapeutics's site. We never take the application ourselves.
Is this posting real?
- This role has been open
- 15 days Entrada Therapeutics's roles stay open a median of 35 days
- Reposted
- No
- Salary listed
- Yes 67% of Entrada Therapeutics's roles list one
- Ghost-job risk at Entrada Therapeutics
- moderate 2 stale, 0 reposted of 9 open
- Hiring momentum
- 14 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 Entrada Therapeutics's own greenhouse board since 2026-08-03. Full hiring picture for Entrada Therapeutics.
About this role
As the Director of Regulatory Writing at Entrada Therapeutics, you will lead the generation of high-quality regulatory documentation to support the advancement of the company's clinical pipeline. This role involves planning and managing the authoring of various regulatory submission components, collaborating with cross-functional teams, and ensuring effective communication with external writing providers. You will also be responsible for developing internal processes and standards critical to regulatory writing.
- benefits
- 4/5
- freshness
- 4/5
- career value
- 4/5
- role clarity
- 4/5
- pay transparency
- 5/5
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 Entrada Therapeutics as an employer.
What you need
- BS or MS with at least 7 years of increasing responsibility as a regulatory/medical writer
- Strong work ethic and excellent communication skills
- Demonstrated track record in medical writing within the pharmaceutical, biotech, or CRO industry
- Expertise with Microsoft Word and eCTD-compliant formatting requirements
- Proficiency in organizing and interpreting complex scientific and clinical data
- Strong understanding of relevant ICH, GCP, and FDA regulatory standards
Nice to have
- Experience working within a biotech company while managing external resources
- Experience with rare diseases, pediatrics, genetic medicines, or leveraging expedited development pathways
- Experience within Duchenne muscular dystrophy or neuromuscular therapeutic areas.
What you get
- Comprehensive health, dental and vision coverage
- Life and disability insurance
- 401(k) match
- Paid, gender-inclusive parental leave
- Holistic support for health and well-being
- Education reimbursement
Worth weighing
- No specific mention of remote work flexibility despite the #LI-Remote tag
- The salary range is stated but may vary based on various factors, which could lead to uncertainty for candidates.
- The role requires a strong commitment to collaboration and a proactive attitude, which may not suit all candidates.
Summarised from Entrada Therapeutics's posting. Read the full original.
Listed by Entrada Therapeutics on their greenhouse job board, last confirmed open on 2026-09-17. PitchMeAI is not the employer.