Global Clinical Trial Project Manager (Internal Medicine)

Worldwide Clinical Trials; Durham (NC); On-site; USD 112,000 - 222,000; Full time

Job summary

Worldwide Clinical Trials is seeking an experienced Project Manager to lead one or more Phase I–IV clinical trials, locally or globally. You will coordinate cross-functional teams and manage resources, schedules, and budgets to ensure on-time, on-budget delivery that meets contract expectations.

The role requires five plus years in clinical pharma or CRO project management, knowledge of ICH/GCP guidelines, and willingness to travel domestically and internationally.

Qualifications

• University/college degree (life science preferred) or certification in allied health.
• 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 requirements, 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.

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.

Skills

Project management

Cross-functional leadership

Communication skills

Planning and organization

Problem solving

Education

Life science degree

Nursing or medical certification

Job description

Worldwide Clinical Trials is seeking an experienced Project Manager to lead one or more Phase I–IV clinical trials, locally or globally. You will coordinate cross-functional teams and manage resources, schedules, and budgets to ensure on-time, on-budget delivery that meets contract expectations.

The role requires five plus years in clinical pharma or CRO project management, knowledge of ICH/GCP guidelines, and willingness to travel domestically and internationally.