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Associate Director of Clinical Operations

NuvalentCambridge, MA / Remote
Remote Full-time

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Experience Level

Mid to Senior

Qualifications

Qualifications include a Master's degree in a related field, with a minimum of 8 years of experience in clinical operations. Proven leadership skills, excellent communication abilities, and a track record of managing complex clinical trials are essential. Familiarity with regulatory guidelines and experience with electronic data capture systems are preferred.

About the job

Nuvalent seeks an Associate Director of Clinical Operations to join the team in Cambridge, MA or work remotely. This leadership role guides the execution of clinical trials, ensuring every step aligns with regulatory standards and internal protocols. The position partners with cross-functional teams to develop and deliver on clinical strategies, overseeing studies from planning through closeout.

What you will do

  • Direct clinical trial operations for multiple concurrent studies
  • Maintain compliance with all regulatory requirements and company procedures
  • Work closely with colleagues across departments to create and implement clinical strategies
  • Supervise all aspects of study management, from initiation to completion
  • Oversee budgets, timelines, and resource planning for clinical programs
  • Mentor and guide junior staff within clinical operations

Requirements

  • Significant experience in clinical operations and project management
  • Background working in pharmaceutical or biotechnology organizations
  • Demonstrated ability to manage budgets and timelines
  • Experience mentoring or managing team members

About Nuvalent

Nuvalent is a pioneering biotechnology company dedicated to developing targeted therapies for patients with cancer. Our focus on innovative research and development enables us to push the boundaries of science and improve patient outcomes.

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