Senior Associate Director, Clinical Scientist (Biotech)

Crispr Therapeutics Inc in; Boston (MA); On-site; USD 170,000 - 185,000; Full time

Benefits offered by this job

Equity

On-site work

Job summary

CRISPR Therapeutics, Inc. in Boston, MA, is seeking an Associate Director, Clinical Scientist to provide scientific input for early and late stage programs.

The role will lead cross-functional efforts across clinical operations, data science, and regulatory affairs to advance gene-editing therapies. You will review trial data, mentor junior scientists, and contribute to regulatory submissions and conference materials.

Qualifications

• Advanced degree (MD/PhD/PharmD/DNP/MSN) with 8–12+ years in clinical or related research.
• Excellent oral and written communication skills and analytical skills.
• Deep expertise in clinical science with a track record in clinical studies.
• Ability to work collaboratively in a fast-paced, matrix environment.
• In-depth understanding of regulatory requirements and guidelines (FDA, EMA, ICH, GCP).

Responsibilities

• Contribute to the scientific development of clinical studies per the clinical development plan.
• Review clinical trial data for safety and efficacy and provide preliminary assessments and recommendations.
• Significantly contribute to the oversight of the clinical study in collaboration with the clinical development lead.
• Present data and information to investigators and governance bodies and regulatory authorities.
• Collaborate with internal stakeholders to translate the clinical protocol into operational deliverables.
• Collaborate with external stakeholders (CROs, investigators) to clarify data submissions.
• Support study execution as the scientific subject matter expert.
• Review and synthesize scientific literature and competitive intelligence to support study and program strategy.
• Develop scientific and protocol training presentations for internal and external meetings.
• Support preparation of scientific material for conference presentations or publications.
• Contribute to the authoring and revision of regulatory submissions.
• Perform analyses and generate scientific slide decks based on datasets.
• Provide mentorship to junior clinical scientists.

Skills

Oral communication

Written communication

Analytical skills

Clinical science expertise

Regulatory knowledge (FDA/EMA/ICH/GCP)

Team collaboration

Experience with medical monitors & etc

Education

MD/PhD/PharmD/DNP/MSN

Job description

CRISPR Therapeutics, Inc. in Boston, MA, is seeking an Associate Director, Clinical Scientist to provide scientific input for early and late stage programs.

The role will lead cross-functional efforts across clinical operations, data science, and regulatory affairs to advance gene-editing therapies. You will review trial data, mentor junior scientists, and contribute to regulatory submissions and conference materials.