Clinical Project Manager

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 (<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.