Senior Clinical Research Associate - Full-Service

Join Syneos Health, a premier biopharmaceutical solutions organization dedicated to accelerating customer success and improving lives through innovative therapies. We are on a mission to put both the customer and the patient at the heart of our work by simplifying and streamlining processes for a more effective partnership. As a Senior Clinical Research Associate, you will collaborate with a team of passionate professionals to help our clients achieve their goals. We thrive in a dynamic environment that demands agility and innovation, driven by our commitment to enhancing lives. Why Choose Syneos Health? We prioritize your personal development through numerous career advancement opportunities, training, and a supportive management team. Our Total Self culture encourages employees to be their authentic selves, fostering a sense of belonging and community within the workplace. We are constantly evolving to create an inclusive workplace that respects diverse perspectives and backgrounds. Key Responsibilities Conduct site qualification, initiation, monitoring, and close-out visits, either on-site or remotely, ensuring compliance with regulatory guidelines and study protocols. Ensure proper documentation of informed consent and safeguard patient confidentiality, while identifying any factors compromising data integrity. Review clinical data, ensuring accuracy in form entries and resolving queries collaboratively with the site staff. Manage investigational product inventory, ensuring compliance with protocol-related dispensing and administration. Maintain the Investigator Site File's accuracy and completeness, ensuring documentation is compliant with regulations. Document site activities and communications thoroughly, supporting patient recruitment and retention efforts. Understand project goals, budgets, and timelines, navigating site communications to meet deliverables effectively. Act as the primary contact for study site personnel, ensuring compliance and training for site team members. Participate in meetings with investigators and project stakeholders, supporting audit readiness and follow-up actions. For Real World Late Phase studies, provide lifecycle site support, train junior staff, and share insights on potential sites based on local knowledge. Qualifications Bachelor's degree or RN in a related field or equivalent experience. Strong knowledge of ICH/GCP guidelines and relevant regulations. Proficient computer skills and openness to new technologies. Exceptional communication and interpersonal skills. Willingness to travel up to 75% regularly. Your Impact at Syneos Health Contribute to groundbreaking clinical trials that have positively impacted patients worldwide. Join us and be part of a team where your efforts make a significant difference in the lives of many. This position may involve work at various sites requiring specific medical and other personal information for facility access. Compensation and Benefits We offer a comprehensive benefits package, which may include a company car or allowance, health benefits, 401k match, employee stock purchase eligibility, commission or bonuses based on performance, and flexible paid time off. Be part of a collaborative environment that empowers you to excel in your career while supporting the well-being of our communities. Join Syneos Health today!

Created: 2026-03-11