Country Study Operations Manager – Sponsor Dedicated

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Syneos Health

WebsiteLinkedInAll Job Openings

10,000+ employees

🧬 Biotechnology

💊 Pharmaceuticals

⚕️ Healthcare Insurance

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.

📋 Description

• 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.

🎯 Requirements

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

🏖️ Benefits

• 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 building an inclusive culture – where you can authentically be yourself. • Driven to Deliver – which captures the passion of our colleagues to show up each day and shape solutions that have the ability to dramatically impact someone’s life. • Continuously building the company we all want to work for and our customers want to work with.