Project Manager

COMPANY DESCRIPTION:   A career here is life-enhancing. At Syner-G, we enable our people to build careers that impact positively on their quality of life. Through our expertise, insight, consulting and management skills, we accelerate breakthrough science and delivery of life-enhancing therapies to more patients. We work across a diverse range of clients and projects, supporting many organizations from the most critical phases of the drug discovery and approval process through to commercialization. It is meaningful, varied and thought-provoking work with a strategic emphasis, a solutions-driven approach and significant, real-world outcomes, from science to delivery/success. To learn more about who we are and what drives us, watch our company video here .  Underpinning this mission is a culture that aligns perfectly with what we want to achieve. We enable our people to grow, we support them in their learning and we reward them in so many different ways. In return, they play an instrumental role in maintaining our reputation across the globe as a strategic biopharma product development and delivery partner. Syner-G was recently honored with BioSpace's prestigious "Best Places to Work" 2026 award, for the third consecutive year, along with many other award-winning programs to make a career here truly life-enhancing. These recognitions are a testament to our commitment to fostering a positive and engaging work environment for our employees, with a particular emphasis on culture, career growth and development opportunities, financial rewards, leadership and innovation.  At Syner-G, we recognize that our team members are our most valuable asset. Join us in shaping the future, where your talents are valued, and your contributions make a meaningful impact.  For more information, visit www.Synergbiopharma.com POSITION OVERVIEW: The Project Manager is responsible for leading and coordinating cross-functional pharmaceutical R&D programs across the drug development lifecycle, from preclinical research through clinical development. This role serves as a central point of coordination among scientific, clinical, regulatory, quality, and operational stakeholders to ensure projects are executed on time, within scope, and within budget. The Project Manager drives project planning, risk management, resource alignment, and operational execution while supporting critical development milestones and regulatory objectives. KEY RESPONSIBILITIES: This list is not exhaustive and may be supplemented and changed as necessary. Develop, maintain, and manage detailed project plans, timelines, and operational roadmaps utilizing tools such as Microsoft Project, Smartsheet, or similar project management platforms. Drive project execution by monitoring deliverables, tracking milestones, and ensuring alignment with overall program objectives and development strategies. Lead cross-functional project meetings involving R&D, Clinical Operations, Regulatory Affairs, Quality, Manufacturing, Supply Chain, and external partners as required. Facilitate communication and collaboration among stakeholders to ensure timely decision-making and effective project execution. Identify critical path activities, project dependencies, potential risks, and operational challenges that may impact project outcomes. Develop and implement risk mitigation strategies, contingency plans, and escalation processes to minimize delays and maintain project momentum. Monitor project budgets, forecast resource requirements, and support financial planning activities throughout the project lifecycle. Evaluate and manage project scope changes while assessing impacts to timelines, budgets, resources, and program objectives. Support preparation and coordination of regulatory submissions, including INDs, CTAs, and other development-related documentation. Partner with Regulatory Affairs and Quality teams to ensure compliance with applicable regulatory requirements, GMP standards, and internal quality systems. Develop project status reports, dashboards, and presentations for leadership and governance meetings. Maintain project documentation, decision logs, action item trackers, and governance records to support transparency and accountability. Coordinate cross-functional activities to ensure successful achievement of key development milestones and objectives. Drive continuous improvement in project management processes, tools, and best practices to enhance program execution and operational efficiency. Other duties as assigned. These job requirements are not intended to be construed as an exhaustive list of all responsibilities, duties, and skills required of personnel. QUALIFICATIONS AND REQUIREMENTS To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the education, experience, skills, knowledge, and abilities required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential duties. Education Bachelor's degree in Life Sciences, Chemistry, Pharmacy, Engineering, or a related scientific discipline required. Advanced degree (MS, PhD, MBA, or equivalent) strongly preferred. Experience Minimum of 5 years of experience within pharmaceutical, biotechnology, or life sciences organizations. At least 3 to 5 years of direct project or program management experience supporting research, development, clinical, or operational initiatives. Experience managing cross-functional teams and projects in a regulated environment. Experience supporting regulatory submissions and development programs is preferred. Demonstrated understanding of pharmaceutical product development, including preclinical, clinical, regulatory, and commercialization activities. Knowledge, Skills, and Abilities Strong understanding of the drug development lifecycle from preclinica