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 supporting late-stage, global clinical trials.

• Demonstrated experience contributing to clinical trial process improvements within a therapeutic area or study team environment

• Industry or academic experience in a relevant therapeutic area and/or clinical trials; experience in large global studies preferred.

• Strong communication and presentation skills, with the ability to clearly convey scientific concepts and clinical data to cross-functional teams and leadership audiences, both written and oral

• Experience supporting the design, monitoring, and implementation of clinical trials in compliance with Good Clinical Practice standards and applicable regulatory requirements

• Working knowledge of study data readout activities, including data cleaning, database lock, data extraction, endpoint validation, and generation of analysis outputs to support topline and final results.

• Experience contributing to regulatory submission documents and supporting clinical regulatory responses for health authority interactions under guidance

• Experience serving as a contributing author on scientific publications or data presentations for internal forums or scientific conferences

• Experience in clinical data review and analysis tools such as Spotfire, listings review platforms, or other data visualization and analysis tools.