Clinical Project Manager

PSI CRO

$100K — $120K *
US-AnywhereRemote in Canada
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree or equivalent combination of education and experience, including 5+ years in pharmaceutical/healthcare and clinical research.
  • Minimum of 5 years of experience in clinical research.
  • At least 2 years of recent experience in a project manager or equivalent role.
  • Experience managing regional clinical projects from start to finish.
  • Preferred therapeutic experience in Oncology, Gastroenterology, or Radiopharmaceuticals.
  • Strong verbal and written communication skills for effective stakeholder engagement.

Responsibilities

  • Manage small clinical research teams on Phase II and III projects.
  • Perform as a regional lead or project co-manager for international studies.
  • Ensure project deliverables meet quality standards on time and within budget.
  • Promote strong customer service principles in all interactions.
  • Lead and train project teams, including CRAs and support staff.
  • Conduct feasibility research to assess study viability.
  • Support business development through proposals and client presentations.

Benefits

  • Focus on professional development and career advancement opportunities.
  • Inclusive company culture that values employee contributions.
Full Job Description
Take your career to the next level and lead challenging full-service clinical research projects in phase II and III, managing the full scope of responsibilities and getting hands-on involvement in every aspect of the study.

Your responsibilities will include:
  • Managing small (
  • Performing regional lead's or project co-manager's role in complex international projects/programs with the secondary responsibility for the production of project deliverables in conformance with the predefined quality standards, on time and on budget.
  • Adhering to and promoting principles of delivery and service in dealing with PSI customers.
  • Leading project teams
  • Training, mentoring, and coaching Lead CRAs, Senior CRAs, CRAs, Project Coordination Associates (PCAs) and Site Management Associates (SMAs)
  • Participating in feasibility research
  • Supporting business development tasks such as proposals, client presentations, bid defense meetings, etc.
  • Implementing company standard practices and complying with intradepartmental procedures


Qualifications
  • Bachelor's degree or an equivalent combination of education, training and experience that presents the required knowledge, skills and abilities. Equivalency is defined as a minimum 5 years of experience gained in pharmaceutical/healthcare industry and clinical research.
  • At least 5-year industry experience in clinical research
  • At least 2-year recent clinical research experience in the capacity of project manager/equivalent (e.g. Clinical Trial Manager, Clinical Study Team Lead, etc.).
  • Regional clinical project management experience, including management of all project services from startup to closure
  • Therapeutic experience in Oncology, Gastroenterology, and/or Radiopharmaceuticals is a plus
  • Excellent communication skills, both written and verbal, with the ability to build strong internal and external stakeholder relationships


Additional Information

Make the right call and take your career to a whole new level. Join the company that focuses on its people and invests in their professional development and success.

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