Senior Clinical Scientist Lead (Hybrid/Remote)

Deciphera Pharmaceuticals Inc.; Waltham (MA); Hybrid; USD 193,000 - 230,000; Full time

Benefits offered by this job

Competitive salary and annual bonus

Comprehensive benefits package

Generous parental leave

Growth opportunities and strong team/c

Outstanding culture and learning

Job summary

Deciphera Pharmaceuticals Inc. is seeking an Associate Director, Clinical Scientist to lead and execute clinical development activities.

You will partner with Medical Directors and cross‑functional study teams to review data, interpret results, and prepare study documents for regulatory submissions. The role requires ensuring data quality, patient safety, and timely study execution across clinical operations, data management, biostatistics, pharmacovigilance, and regulatory functions.

Qualifications

• PhD or equivalent degree with 2+ years of relevant experience, or bachelor’s/master’s degree with 5+ years of relevant post‑graduate experience, including pharmaceutical industry experience in clinical drug or biologics development.
• Experience as a Clinical Scientist or in a comparable clinical development role with the ability to work independently.
• Hands‑on experience reviewing, analyzing, and interpreting clinical trial data.

Responsibilities

• Clinical Data Review & Study Execution: Lead ongoing clinical data review to support data quality, interpretation, and patient safety.
• Identify and escalate clinically relevant findings and partner with study teams to resolve data‑related issues.
• Collaborate with Data Management and Clinical Operations on study implementation and EDC development.

Skills

Clinical Data Review

Data Management

Biostatistics

Pharmacovigilance

Regulatory

Cross-functional Leadership

Scientific Communication

Study Execution

Education

PhD or equivalent

Bachelor's or Master's with 5+ years post‑graduate experience

Job description

Deciphera Pharmaceuticals Inc. is seeking an Associate Director, Clinical Scientist to lead and execute clinical development activities.

You will partner with Medical Directors and cross‑functional study teams to review data, interpret results, and prepare study documents for regulatory submissions. The role requires ensuring data quality, patient safety, and timely study execution across clinical operations, data management, biostatistics, pharmacovigilance, and regulatory functions.