Sr Project Manager/ Clinical Trial Manager

OverviewSr Project Manager/ Clinical Trial Manager - Oncology at Syneos Health. Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success in clinical development, medical affairs and commercial insights. ResponsibilitiesProject Leadership and Delivery: Manage a project as Project Manager for interdisciplinary clinical research programs ensuring compliance with Good Clinical Practices (GCPs), SOPs, and regulatory requirements. Act as primary liaison between the Company and the Customer to ensure project launch, conduct, and closeout per contractual agreements. Lead clinical team to ensure quality, timelines and budget management. Accountable for the financial performance and all project deliverables for assigned projects and/or regions. Coordinate activities and deliverables of all project conduct partners and proactively identify and manage issues. Reporting and Communication: Maintain project information in databases and systems. Monitor project progress using timelines and tracking/analysis tools. Ensure project management components of inspection readiness, including Trial Master Files. Develop and implement project plans in accordance with Controlled Documents. Prepare, coordinate, and present project material at internal and external meetings. Direct the activities of Project Support staff; mentor project management team members and clinical staff; facilitate team building and communication. Prepare project management reports for clients and management. Implement resource strategies and develop contingency planning and risk mitigation strategies to ensure successful delivery. Business Development: Participate in bid defense meetings as potential project manager/director. Build strong relationships with current clients to generate new or add-on business. Maintain awareness of the therapeutic environment and drug development trends. Management: May train and support new Project Managers; may line manage other project management team members and clinical monitoring staff. QualificationsBachelor’s Degree (or equivalent) in life sciences, Medicine, Pharmacy, Nursing or related field or equivalent combination of education and experience. Strong knowledge of Good Clinical Practice/ICH guidelines, regulatory requirements, drug development process and clinical monitoring procedures. Clinical research organization (CRO) experience and relevant therapeutic experience preferred. Strong time management and ability to work independently. Comfortable with embracing new technologies. Excellent written and verbal communication, presentation, and interpersonal skills. Ability to mentor and manage new staff and handle multiple tasks to meet deadlines, delivering high-quality work in a dynamic environment. Travel availability as necessary (approximately 25%). Benefits and Other InformationSalary range: base salary range represents the anticipated low and high for this position. Actual salary varies based on qualifications, skills, and proficiency for the role. Benefits may include a company car or car allowance, health benefits (Medical, Dental, Vision), 401k with company match, eligibility for Employee Stock Purchase Plan, potential for commissions/bonus based on performance, flexible PTO and sick time in accordance with applicable laws. Syneos complies with paid sick time requirements where permitted. Additional information: The Company may assign other tasks at its sole discretion. This content is intended to comply with applicable laws and reflects the responsibilities and qualifications for the role. #J-18808-Ljbffr