Overview Project Manager Syneos Health® is a life sciences services organization that partners with innovators across the drug development and commercialization continuum to accelerate progress. The Clinical Solutions team applies deep expertise to understand customer needs and shape effective solutions. Depending on the engagement model, you will collaborate with problem solvers to deliver results for customers and patients. Responsibilities Project Leadership and Delivery: Manage interdisciplinary clinical research studies, ensuring compliance with GCP, applicable SOPs, and regulatory requirements. Act as primary liaison between the Company and the Customer to ensure timely study launch, conduct, and closeout per contractual agreements. Lead project team to ensure quality, timelines, and budget management. Accountable for financial performance of each project; coordinate activities of all study conduct partners and proactively identify and manage issues. Ensure studies are conducted in compliance with GCP, SOPs, and regulatory requirements; accountable for all project deliverables. Responsible for quality and completeness of TMF for assigned projects. Maintain study information on various databases and systems. Oversee study management components of inspection readiness; develop and implement project plans. Plan, coordinate, and present at internal and external meetings; prepare project management reports for clients and management. Develop contingency planning and risk mitigation strategies to ensure successful delivery of study goals. Develop strong relationships with current clients to generate new or add-on business. May participate in bid defense meetings as a potential project manager. May line-manage other project management team members and clinical monitoring staff. Qualifications Bachelor’s Degree (or equivalent) in life sciences, Medicine, Pharmacy, Nursing, or equivalent combination of education and experience. Clinical research organization (CRO) and relevant therapeutic experience preferred; strong knowledge of GCP/ICH and regulatory requirements. Strong organizational and time-management skills; ability to work independently. Direct therapeutic area expertise. Ability to embrace new technologies. Excellent communication, presentation, and interpersonal skills, written and spoken. Ability to travel as necessary (approximately 25%). Notes Additional information: Tasks, duties, and responsibilities are not exhaustive. The company may assign other tasks as needed. Qualifications may differ if equivalent experience is used. The organization complies with applicable laws and policies, including the Americans with Disabilities Act with reasonable accommodations when appropriate. #J-18808-Ljbffr