Project Manager leading Phase I–IV clinical trials for global CRO Worldwide Clinical Trials. Coordinating cross-functional teams, budgets, risks, and client delivery from start-up through close-out.
Responsibilities
Lead cross-functional project teams and coordinate internal and external partners, including subcontractors, to deliver assigned clinical trials
Manage project resources with functional leaders, identifying needs and developing contingency plans
Oversee financial performance of assigned projects and work toward established financial targets
Anticipate project risks and complex issues
Develop contingency and recovery strategies and drive solutions through implementation
Build relationships with client project teams and act as a key point of contact
Support client satisfaction and operational excellence
Promote teamwork across a matrix environment, resolve conflicts, and maintain clear communication
Ensure team members are trained and follow study protocols, applicable SOPs, GCP, and local regulations
Drive improvements to enhance project efficiency and quality
Collaborate with global teams across multiple time zones
Travel approximately 10%
Requirements
University or college degree, preferably in life sciences; certification in a related allied health profession; or equivalent combination of education and experience
At least five years of clinical pharmaceutical industry experience, including demonstrated competency in clinical project management
Alternatively, more than five years of supervisory experience in a healthcare setting combined with four years of clinical research experience in the pharmaceutical or CRO industries may be considered
Proven relevant clinical development experience and skills may be considered
Thorough knowledge of clinical project management processes
Ability to manage multiple competing priorities and resources effectively
Thorough knowledge of ICH Guidelines and GCP, including international regulatory requirements governing clinical development programs
Broad knowledge of the drug development process and client needs
Strong problem-solving, planning, organizational, and computer skills
Strong leadership and interpersonal skills
Ability to motivate matrix teams, work independently, resolve challenges, and negotiate professionally with clients
Valid current passport and driver's license
Ability to drive and undertake domestic and international travel, including overnight stays
Proficiency in English and French, both written and verbal
Benefits
Collaborative and inclusive work environment
Growth and career development opportunities
Opportunity to learn and grow
Remote work arrangement
Opportunity to contribute to life-changing clinical research
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