Description

You will ensure excellence in clinical trial planning, execution, and data collection in accordance with regulatory guidelines at Nuvalent, an early-stage oncology biotech. You'll manage site selection, contracts, budgets, and vendor partnerships to deliver high-quality clinical trial results.

Requirements

• 5–7 years of Clinical Operations experience.
• Bachelor’s degree or higher in scientific or healthcare discipline preferred.
• Extensive knowledge of current ICH-GCP guidelines.
• Relevant experience managing early through late phase clinical trials.
• Able to thrive in a remote/virtual environment.

Responsibilities

• Contribute to one or multiple clinical studies and demonstrate thorough knowledge of clinical operations project management.
• Collaborate with cross-functional clinical study team to support clinical study delivery.
• Evaluate and ensure appropriate oversight of CROs and other external vendors.
• Ensure clinical trials are executed according to scope of work, budget, timelines, KPIs, and corporate goals.
• Oversee and manage creation, maintenance, QC, and close out of TMF activities.