Clinical Project Manager leading full-service phase II/III clinical trials for PSI, a contract research organization. Managing project delivery, teams, budgets, and international study operations.
Responsibilities
Manage small projects under direct or general supervision, with responsibility for producing project deliverables to predefined quality standards, on time and on budget
Perform regional lead or project co-manager responsibilities in complex international projects/programs
Adhere to and promote PSI delivery and service principles when working with 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
Lead full-service phase II and III clinical research projects
Requirements
Bachelor's degree or an equivalent combination of education, training and experience
Equivalent qualification: minimum 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 or 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
Ability to build strong internal and external stakeholder relationships
Therapeutic experience in Oncology, Gastroenterology, and/or Radiopharmaceuticals is a plus
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