Project Specialist, Clinical Research

November 6

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Syneos Health

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Biotechnology • Pharmaceuticals • Healthcare Insurance

Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. They translate unique clinical, medical affairs, and commercial insights into outcomes to address modern market realities. By utilizing advanced technologies and insights, Syneos Health collaborates with clients to speed the delivery of important therapies to patients worldwide, offering services that span the entire clinical-to-commercial spectrum.

10,000+ employees

🧬 Biotechnology

💊 Pharmaceuticals

⚕️ Healthcare Insurance

📋 Description

• Planning, directing, creating, and communicating clinical study timelines, ensuring that all milestones are met and that the project stays on track • Gathering input from cross-functional teams, including clinical, regulatory, and data management, to create comprehensive plans for timely deliverables • Ensuring consistency of clinical study processes across trials by standardizing procedures and implementing best practices • Overseeing and resolving operational aspects of clinical trials, including addressing any issues that arise during the study and ensuring that all activities are conducted in compliance with SOP, GCP, and specific country regulations • Selecting sites and vendors for clinical trials, negotiating contracts, and managing relationships to ensure high-quality and timely delivery of services • Preparing clinical trial budgets, monitoring expenditures, and ensuring that the study remains within budget • Monitoring progress of clinical trials, tracking key performance indicators, and following up with team members and line managers to address any deviations from the plan • Implementing and preparing the clinical development strategy as outlined by the clinical teams, ensuring alignment with overall project goals and objectives • Developing trial recruitment strategies, including identifying target populations, creating recruitment materials, and monitoring enrollment progress

🎯 Requirements

• High school diploma or equivalent required • Associate's degree or higher in a related field preferred • Minimum of 3 years of experience in clinical project management or a related field • Strong understanding of clinical trial processes and regulations • Experience with SOP, GCP, and country-specific regulations • Certification in Clinical Project Management or related field preferred • Good Clinical Practice (GCP) certification preferred

🏖️ Benefits

• Professional development opportunities • Career development and progression • Supportive and engaged line management • Technical and therapeutic area training • Peer recognition and total rewards program