Clinical Project Manager

PSI CRO; United States; On-site; USD 120,000 - 180,000; Full time

Job summary

PSI CRO is seeking a senior project manager to lead challenging full-service clinical research projects in phase II and III, coordinating all study aspects from startup to closure. You will manage multi-country studies, promote PSI delivery standards, and provide hands-on leadership across project teams.

The role requires at least 5 years in clinical research, strong communication, and experience mentoring CRAs and PMs.

Qualifications

• Bachelor's degree or equivalent with 5 years of pharma/healthcare/clinical research experience.
• At least 5 years industry experience in clinical research.
• At least 2 years recent clinical research experience as project manager/equivalent.
• Regional clinical project management experience including startup to closure.
• Therapeutic experience in Oncology/Gastroenterology/Radiopharmaceuticals is a plus.

Responsibilities

• Manage small projects (≤5 countries) ensuring deliverables meet quality, time and budget.
• Perform regional lead’s or co-manager role on complex international projects with deliverables.
• Adhere to PSI delivery principles and promote service standards.
• Lead project teams and coordinate activities.
• Train, mentor and coach Lead CRAs, Senior CRAs, CRAs, PCAs and SMAs.
• Support feasibility research and business development tasks (proposals, client presentations).
• Implement company standard practices and intradepartmental procedures.

Skills

Project management

Leadership

Communication

Education

Bachelor's degree

Job description

PSI is a leading Contract Research Organization with 30 years in the industry offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications.

Job Description

Take your career to the next level and lead challenging full-service clinical research projects in phase II and III, managing the full scope of responsibilities and getting hands‑on involvement in every aspect of the study.

Your responsibilities will include:

• Managing small (<5 countries and/or limited services) projects under direct or general supervision, with primary responsibility for the production of project deliverables in conformance with the predefined quality standards, on time and on budget
• Performing regional lead’s or project co-manager’s role in complex international projects/programs with the secondary responsibility for the production of project deliverables in conformance with the predefined quality standards, on time and on budget.
• Adhering to and promoting principles of delivery and service in dealing with PSI customers.
• Leading project teams
• Training, mentoring, and coaching Lead CRAs, Senior CRAs, CRAs, Project Coordination Associates (PCAs) and Site Management Associates (SMAs)
• Participating in feasibility research
• Supporting business development tasks such as proposals, client presentations, bid defense meetings, etc.
• Implementing company standard practices and complying with intradepartmental procedures

Qualifications

• Bachelor's degree or an equivalent combination of education, training and experience that presents the required knowledge, skills and abilities. Equivalency is defined as a minimum 5 years of experience gained in pharmaceutical/healthcare industry and clinical research.
• At least 5-year industry experience in clinical research
• At least 2-year recent clinical research experience in the capacity of project manager/equivalent (e.g. Clinical Trial Manager, Clinical Study Team Lead, etc.).
• Regional clinical project management experience, including management of all project services from startup to closure
• Therapeutic experience in Oncology, Gastroenterology, and/or Radiopharmaceuticals is a plus
• Excellent communication skills, both written and verbal, with the ability to build strong internal and external stakeholder relationships

Additional Information

Make the right call and take your career to a whole new level. Join the company that focuses on its people and invests in their professional development and success.