Clinical Project Manager

PSI CRO

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

Qualifications

  • Bachelor's degree or equivalent experience in pharmaceutical/healthcare industry and clinical research (minimum 5 years)
  • At least 5 years of industry experience in clinical research
  • Minimum 2 years of recent experience as a project manager or equivalent
  • Experience managing all project services from startup to closure
  • Preferred experience in Oncology, Gastroenterology, and/or Radiopharmaceuticals
  • Strong verbal and written communication skills

Responsibilities

  • Manage small to complex international clinical research projects
  • Perform regional lead or project co-manager roles
  • Ensure project deliverables meet quality standards, timelines, and budgets
  • Lead and mentor project team members including CRAs and PCAs
  • Conduct feasibility research for new projects
  • Support business development through proposals and client presentations
  • Implement and comply with company practices and procedures

Benefits

  • Focus on employee professional development and success
  • Engagement in challenging full-service clinical research projects
  • Hands-on involvement in all study aspects
  • Opportunity to lead and mentor within a supportive environment
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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