Project Manager, Internal Medicine- Metabolic Live Diseases (US)

We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence. We are a global team of over 3,500+ experts, bright thinkers, dreamers and doers, and together, we are changing the way the world experiences CROs.

About the role

The Project Manager (PM) will manage one or more allocated Phase I through IV Clinical Trials that may be local, regional or global in scope. WCT Project Managers are 100% accountable for the success of their projects. The PM is responsible for the overall coordination and management of clinical trials from start up through close out activities, directing the technical, financial and operational aspects to secure successful completion. The PM works with functional area leads to identify and evaluate fundamental project requirements, interpret data on complex issues, implement contingency planning and rescue strategies where needed, and ensure solutions are implemented. The PM ensures all project deliverables meet the customer’s time, quality, and cost expectations.

Responsibilities

• Lead core project team members and facilitate their ability to lead extended/complete project team
• Lead cross-unit coordination both internal and external, inclusive of sub-contractors
• Define and manage project resource needs in conjunction with functional heads and establish contingency plans for key resources
• Ensure successful design, implementation, tracking and revision of project plans for assigned projects
• Promote effective teamwork among project team members; resolve conflicts as needed
• Ensure appropriate communication on project-related matters with the PM Management

Requirements

• University/college degree (life science preferred) or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing certification, medical or laboratory technology) or equivalent combination of education and experience that provides the required knowledge, skills and abilities
• Minimum of five (5) years of clinical pharmaceutical industry experience including demonstrated skills and competency in clinical project management tasks
• In lieu of the above, candidates with > five (5) years supervisory experience in a health care setting and four (4) years clinical research experience in the pharmaceutical or CRO industries will be considered and/or proven ability and demonstration of relevant experience and skills in clinical development
• Thorough knowledge of project management processes
• Thorough knowledge of ICH Guidelines and GCP including international regulatory requirements for the conduct of clinical development programs
• 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 in English, both written and verbal
• Broad knowledge of drug development process and client needs

Skills

• Experience in managing projects in a multi-office environment
• Demonstrated ability to handle multiple competing priorities; utilize resources effectively
• Demonstrated ability to inspire effective teamwork and motivate staff within a matrix system
• Demonstrated ability to lead by example and encourage team members to seek solutions
• Excellent communication, planning and organizational skills

Pay

The salary range for this position is $112,000.00 - $222,000.00 annually. The final salary will be determined based on relevant experience, performance, education, and internal equity. In addition to base salary, we offer a competitive benefits package depending on location.