Clinical Project Manager

Our take on this role

About this role

Manage phase II and III clinical research projects, leading study teams and delivering work on time, within budget and to defined quality standards. Responsibilities include smaller projects and regional leadership or co-management of complex international studies.

What could you bring from clinical work?

• Nurses: Experience caring for patients with cancer or gastrointestinal conditions may inform clinical research project management in those therapeutic areas.
• OTs: Your experience coordinating multidisciplinary rehabilitation teams could help with leading clinical research project teams.
• PTs: Evaluating evidence, patient populations and rehabilitation workflows could help you contribute to study feasibility research.
• SLPs: Teaching clinical procedures and checking understanding may help you train and coach research staff.
• Social workers: Coordinating communication among patients, families and interdisciplinary providers could help you build relationships with internal and external study stakeholders.

Full job description from PSI CRO

Company 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 ( 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.