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PSI CRO AG

Clinical Project Manager

PSI CRO AG

. Manage small projects under direct or general supervision, with primary responsibility for producing project deliverables according to predefined quality standards, on time and on budget .

Posted 10/14/2026full-timeRemote • United StatesMid-LevelSeniorWebsite

Core Competencies

Role fit
Core Competencies

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Demonstrates expertise in managing clinical research projects within the pharmaceutical and healthcare industries, ensuring adherence to quality standards and timelines. Proficient in training and mentoring project teams while fostering strong stakeholder relationships.

Highest-signal resume keywords
Clinical Project ManagementClinical Research ExperienceStakeholder Relationship ManagementProject Deliverables ManagementTraining and Mentoring

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills
Project ManagementClinical Trial ManagementFeasibility ResearchBid DefenseProposal Development
Soft Skills
Excellent Communication SkillsTeam Leadership
Industry Keywords
Pharmaceutical IndustryHealthcare IndustryOncologyGastroenterologyRadiopharmaceuticals

About the role

Key responsibilities & impact
  • Manage small projects under direct or general supervision, with primary responsibility for producing project deliverables according to predefined quality standards, on time and on budget
  • Perform regional lead or project co-manager responsibilities in complex international projects/programs, with secondary responsibility for project deliverables
  • Adhere to and promote delivery and service principles when dealing with PSI customers
  • Lead project teams
  • Train, mentor, and coach Lead CRAs, Senior CRAs, CRAs, PCAs, and SMAs
  • Participate in feasibility research
  • Support business development through proposals, client presentations, and bid defense meetings
  • Implement company standard practices and comply with intradepartmental procedures

Requirements

What you’ll need
  • Bachelor's degree or an equivalent combination of education, training and experience
  • Equivalency requires a minimum of 5 years of experience in the pharmaceutical/healthcare industry and clinical research
  • At least 5 years of industry experience in clinical research
  • At least 2 years of recent clinical research experience as a project manager/equivalent, such as Clinical Trial Manager or Clinical Study Team Lead
  • Regional clinical project management experience, including management of all project services from startup to closure
  • Excellent written and verbal communication skills, with the ability to build strong internal and external stakeholder relationships
  • Therapeutic experience in Oncology, Gastroenterology, and/or Radiopharmaceuticals is a plus

Benefits

Comp & perks
  • Professional development and success investment
  • Remote work