Clinical Project Manager

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.

Lead phase II and III clinical research projects, ensuring deliverables are produced on time, on budget, and according to quality standards. Responsibilities include managing project teams, mentoring staff, and supporting business development tasks like bid defense meetings.

Requires a bachelor's degree and at least 5 years of clinical research experience, with at least 2 years specifically in a project management role. Experience in regional clinical project management and therapeutic knowledge in Oncology or Gastroenterology is preferred.

• Team LeadershipPreferred
• Communication SkillsPreferred
• Stakeholder ManagementPreferred
• Business developmentPreferred

Identified from the job description. Confirm important requirements above.

• Clinical Project Management
• Clinical Research
• Project Deliverables
• Team Leadership
• Mentoring
• Feasibility Research
• Business Development
• Stakeholder Management
• Budget Management
• Quality Standards
• Oncology
• Gastroenterology
• Radiopharmaceuticals
• Communication Skills
• Clinical Trial Management

• Healthcare
• Management & Leadership
• Science & Research
• Manufacturing

Minimum education

Bachelor’s degree

Minimum experience

5+ years

Posting language

English

Working hours

40 hours per week

Seniority

Mid-Senior level

Application method

Direct apply is available