Why Syneos Health • We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program. • We are committed to our Total Self culture – where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people. • We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives – we’re able to create a place where everyone feels like they belong.

• Develop and coordinate Phase 1 clinical research studies, ensuring all aspects of the study are meticulously planned and executed • Implement clinical research protocols and ensure compliance with regulatory requirements, including Good Clinical Practice (GCP) guidelines • Collaborate with principal investigators, research subjects, client teams, and clinic operations teams to facilitate smooth communication and coordination • Plan and manage logistics and resource usage for clinical trials, including scheduling, budgeting, and resource allocation • Track study progress and ensure alignment with project milestones, client deliverables, and budget, providing regular updates to stakeholders • Prepare and present study reports and updates to stakeholders, including detailed analysis of study data and progress • Ensure adherence to global and regional regulations and guidelines, staying up-to-date with any changes or updates • Provide guidance and support to lower-level professionals and team members, fostering a collaborative and supportive work environment • Identify and resolve any issues or challenges that arise during the course of the study, ensuring timely and effective solutions • Maintain accurate and comprehensive documentation of all study-related activities, ensuring transparency and accountability

Qualifications: • Bachelor's degree in a related field (e.g., life sciences, clinical research) • Minimum of 3 years of experience in clinical trial management or a related field • In-depth knowledge of clinical research processes and regulations • Strong project management and organizational skills • Excellent communication and interpersonal skills • Ability to work independently and as part of a team • Proficiency in using clinical trial management software and tools Necessary Skills: • Strong analytical and problem-solving skills Attention to detail and accuracy • Ability to manage multiple projects and priorities simultaneously • Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint) • Knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements • We are always excited to connect with great talent. This posting is intended for an possible upcoming opportunity rather than a live role. By expressing your interest, you'll be added to our talent pipeline and considered should this role become available.

Certifications: • Certified Clinical Research Professional (CCRP) or equivalent certification preferred

For more details, please refer to the company website.