Associate Director, Clinical Trial Management

This is a fully remote position, open to applicants in Canada.

📋 Description

• Oversee and ensure responsibility for daily project operations in alignment with the contract, ICH/GCP, and relevant laws and regulations.

• Act as the main point of contact for the Sponsor regarding operational project-specific matters and study deliverables.

• Maintain a thorough understanding of the protocol, therapeutic area, and indication.

• Provide comprehensive oversight of internal project team members and their deliverables.

• Ensure that essential project-specific training is delivered.

• Review and offer feedback on study protocols, edit check specifications, data analysis plans, and final study reports as necessary.

• Create operational project plans.

• Manage risk evaluation and implementation.

• Oversee study vendors as necessary.

• Supervise site quality and monitoring deliverables.

⛳️ Requirements

• A Bachelor’s degree in a health-related field is required.

• An advanced degree in a health-related field is preferred.

• Experience in Phases 1–4; Phases 2–3 experience is preferred.

• A minimum of 5 years of experience as a project/clinical trial manager within a CRO is required.

• Proven experience in managing overall project timelines.

• Experience with bid defense.

• Strong leadership abilities.

🏝️ Benefits

• Comprehensive health, wellness, retirement, and PTO benefits.

• Competitive compensation programs that acknowledge and reward performance.

• Office-based environment with on-site mentors.

• Clearly defined career paths with distinct advancement opportunities.

• Industry-leading onboarding and training programs.

• Continuous training and learning opportunities.

• Company-sponsored social events.

• Flexible work arrangements: home-based position in Canada with occasional WFH flexibility for eligible roles after training.