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Senior Clinical Project Manager

Posted on Feb 7, 2021 by Investigo Change Solutions

New York, NY 10001
Immediate Start
$150k - $150k Annual


Remote - United States

Seeking a dynamic and highly experienced Sr. Clinical Project Manager to join a small group within a full-service CRO pharmaceutical-setting. Searching for an experienced & confident CPM to join a small team where you'll have the opportunity to impact the business and shape the culture of the company. Someone who's highly motivated & enjoys working in a start-up mode to help create processes, revise SOPs, & more, would do well in this role.


  • Lead and manage the business with all clinical trial projects studies, and drive plans and strategies.

  • Oversees all clinical study activities and ensure strategy, support, implementation, and execution of trial studies per company plans and timelines, and budget for clinical studies within multiple clinical programs.

  • Work with and support management with strategies on studies or programs.

  • Lead and manage the operational aspects for implementation and global trial studies activities from study viability to CSR, regulatory requirements, GCPs, and SOPs.

  • Skilled in handling complex or difficult situations (or trial projects) to meet the goals of the study.

  • Will be responsible for managing the activities and deliverables of all study content by providing effective study reporting, submission activities, audits, and inspections.


  • Advanced degree in a Scientific discipline required; medical graduate or other life science (MD, Ph.D)

  • Strong working experience/knowledge in Clinical Research (7-8 years) with relevant Project Management experience with clinical development studies (5 years) in a pharma setting.

  • In-depth knowledge of regulatory requirement (ICH E6, GCP, EU Directive)

  • Prior experience leading, managing, and developing CROs and any other external partnerships.

  • Oncology therapeutic focus is strongly desired.

  • Prior experience working in a Matrix environment.

  • Leadership and prior management experience.

  • Strong presentation, communication, and interpersonal skills.

  • Broad knowledge of drug development process and has strong relationships with the investigators.

If interested in learning more, please contact Bria Gaber at (see below) or call for more information.

Reference: 1087203671

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