About the role

Project Manager leading Phase I–IV clinical trials for global CRO Worldwide Clinical Trials. Coordinating teams, resources, deliverables, and regulatory-compliant execution.

Responsibilities

Manage one or more allocated Phase I through IV clinical trials with local, regional, or global scope
Coordinate and manage clinical trials from start-up through closeout
Direct the technical, financial, and operational aspects of projects
Identify and evaluate project requirements, interpret complex data, and develop contingency plans and rescue strategies
Ensure project deliverables meet customer time, quality, cost, and contract expectations
Lead core project team members and facilitate leadership of extended or complete project teams
Lead internal and external cross-unit coordination, including subcontractors
Define and manage project resource needs with functional heads and establish contingency plans
Design, implement, track, and revise project plans
Promote effective teamwork and resolve conflicts
Ensure appropriate communication with Project Management leadership

University/college degree (life science preferred) or certification in a related allied health profession from an appropriately accredited institution, or equivalent combination of education and experience
Minimum of five (5) years of clinical pharmaceutical industry experience, including clinical project management tasks
Alternatively, more than five (5) years of supervisory experience in a health care setting and four (4) years of clinical research experience in the pharmaceutical or CRO industries, or proven relevant clinical development experience and skills
Experience managing projects in a multi-office environment
Ability to handle multiple competing priorities and utilize resources effectively
Ability to inspire teamwork and motivate staff within a matrix system
Ability to lead by example and encourage team members to seek solutions
Excellent communication, planning, and organizational skills
Self-motivated with excellent problem-solving skills
Thorough knowledge of project management processes
Thorough knowledge of ICH Guidelines and GCP, including international regulatory requirements
Available for domestic and international travel, including overnight stays
Valid current passport required
Ability to drive and have a valid driver’s license
Fluent in local office language and English, written and verbal
Broad knowledge of drug development processes and client needs