Clinical Scientist Associate Director

Career Category

Job Description

What you will do

In this role, the Clinical Scientist Associate Director supports the design, execution, and oversight of clinical trials and other late-phase global clinical studies. The role contributes to protocol development, study execution, medical monitoring support, and clinical data review, ensuring delivery of high-quality, decision-ready clinical data for regulatory submissions and scientific dissemination.

Support the design, start-up, and execution of global clinical trials, ensuring adherence to protocol, regulatory requirements, and data integrity standards.

Contribute to development of clinical protocols, statistical analysis plans, investigator brochures, and regulatory documents, with focus on study endpoints, key efficacy outcomes, and safety assessments.

Collaborate with cross-functional teams to support endpoint strategy, event adjudication processes, and safety monitoring.

Participate in development and oversight of endpoint adjudication charters, safety monitoring plans, and Data Monitoring Committee (DMC) interactions.

Provide clinical input into data management plans, CRF design, and clinical data review, with focus on key study endpoints, efficacy and safety outcomes, and/or imaging or biomarker endpoints, as applicable.

Conduct ongoing clinical data review and signal detection, supporting identification and resolution of safety and data quality issues across global trial sites.

Support preparation and interpretation of interim analyses, database lock activities, and top-line data readouts.

Assist Development Lead and Clinical Scientist Director with medical monitoring activities and oversight of CROs, vendors, and adjudication committees.

Collaborate with clinical operations, biostatistics, safety, regulatory, and medical affairs teams to ensure successful delivery of clinical studies across relevant indications and endpoint strategies.

Contribute to clinical study reports, regulatory submissions, scientific publications, and presentations for internal and external stakeholders.

Identify operational or scientific risks and proactively implement mitigation strategies across cross-functional teams.

What we expect of you

We are all different, yet we all use our unique contributions to serve patients. The dynamic professional we seek is a leader with these qualifications.

Basic Qualifications:

Doctorate degree and 3 years of life sciences/healthcare experience

OR

Master’s degree and 5 years of life sciences/healthcare experience

OR

Bachelor’s degree and 7 years of life sciences/healthcare experience

Preferred Qualifications:

3 years of pharmaceutical clinical drug development experience, including experience suppor