Clinical Scientist — Neuromuscular Trials & Data Lead

Entrada Therapeutics, Inc.; Boston (MA); Remote; USD 120,000 - 180,000; Full time

Job summary

Entrada Therapeutics is seeking a highly motivated clinical researcher to lead and support data review across all phases of Duchenne and rare disease programs, leveraging Entrada’s EEV technology. The role emphasizes designing strategies for clinical trials, data interpretation, and cross-functional collaboration with Medical Directors, Data Management, and Biostatistics.

The candidate should have a strong background in GCP/ICH and a track record of delivering high-quality study reports, safety,

Qualifications

• Ph.D., PharmD, MD, Nursing, or Clinical Master’s degree in a scientifically relevant field with 6+ years clinical development experience.
• Proven understanding of clinical development processes for phase 1-3 studies.
• Experience identifying trends and setting risk mitigation strategies with Medical teams.
• Strong knowledge of GCP/ICH guidelines and regulatory expectations.

Responsibilities

• Support interpretation of clinical data to generate high quality summaries for regulatory filings, publications, and scientific communications.
• Collaborate cross-functionally with Medical Directors, Clinical Operations, Data Management, Biostatistics, and Business Operations to drive execution across clinical phases.
• Lead or support authoring of selected sections of clinical study reports in partnership with Medical Directors.
• Perform safety and efficacy reviews to prepare for DMC, analyzing trends within programs.

Skills

Clinical data review

Data analysis

Data visualization

Regulatory filings

Cross-functional collaboration

GCP/ICH knowledge

Education

Ph.D., PharmD, MD, Nursing, or Clinical Master’s degree

Tools

Microsoft Excel

CRF design tools

Data review tools

Job description

Entrada Therapeutics is seeking a highly motivated clinical researcher to lead and support data review across all phases of Duchenne and rare disease programs, leveraging Entrada’s EEV technology. The role emphasizes designing strategies for clinical trials, data interpretation, and cross-functional collaboration with Medical Directors, Data Management, and Biostatistics.

The candidate should have a strong background in GCP/ICH and a track record of delivering high-quality study reports, safety,