Remote Clinical Scientist — DMD & Neuromuscular Trials

Entrada Therapeutics Inc.; Boston (MA); Remote; USD 150,000 - 210,000; Full time

Job summary

Entrada Therapeutics, Inc. seeks a seasoned clinical development professional to lead strategic data review across Duchenne-focused programs, leveraging Entrada’s EEV technology.

You will design and implement data review strategies, coordinating with Medical Directors, Data Management, Biostatistics and Operations to support trials from early phases through pivotal studies. You will drive quality and regulatory submissions in a fast-paced, mission-driven environment, ensuring scientific rigor

Qualifications

• Ph.D., PharmD, MD, Nursing, or Clinical Master’s degree with 6+ years in biotech/pharma.
• Strong understanding of clinical development processes for Phase 1-3.
• Experience identifying trends and risk mitigation with Medical teams.

Responsibilities

• Support interpretation of clinical data to generate high quality summaries and insights for regulatory filings and publications.
• Collaborate with Medical Directors, Clinical Operations, Data Management, Biostatistics and Business Operations to drive cross-functional execution.
• Lead or support authoring sections of clinical study reports with Medical Directors.
• Perform safety and efficacy reviews and assess protocol compliance with escalation as needed.
• Design study CRFs and guidelines, ensuring alignment with study requirements during testing.
• Prepare for DMC reviews with data trends analysis and stakeholder collaboration.
• Develop and innovate data access, retention, and visualization strategies to support trend identification.

Skills

Clinical data review

Data analysis

Data visualization

Scientific communication

Cross-functional collaboration

Education

Ph.D.

PharmD

MD

Nursing

Clinical Master’s degree

Tools

Microsoft Office

Data review tools

Job description

Entrada Therapeutics, Inc. seeks a seasoned clinical development professional to lead strategic data review across Duchenne-focused programs, leveraging Entrada’s EEV technology.

You will design and implement data review strategies, coordinating with Medical Directors, Data Management, Biostatistics and Operations to support trials from early phases through pivotal studies. You will drive quality and regulatory submissions in a fast-paced, mission-driven environment, ensuring scientific rigor