Principal Clinical Trial Regulatory Affairs – CTRA

Syneos Health

Principal Clinical Trial Regulatory Affairs at Syneos Health, ensuring compliance with clinical trial regulations. Collaborating internally and externally to manage regulatory submissions and relationships.

Posted 5/26/2026full-timeBelgrade • 🇷🇸 SerbiaLeadWebsite

About the role

Key responsibilities & impact

Collaborate with internal teams to ensure regulatory compliance for clinical trials
Prepare and submit regulatory documents to health authorities
Liaise with regulatory agencies and manage relationships
Monitor changes in regulations and update policies as needed
Provide training and guidance on regulatory matters

Requirements

What you’ll need

Experience in Clinical Trial Regulatory Affairs
In-depth knowledge of regulatory guidelines and requirements
Strong analytical and problem-solving skills
Excellent communication and interpersonal skills
Must be fluent in English.

Benefits

Comp & perks

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. Central to this is our purpose – 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.
We’re a growing, global company dedicated to advancing our talent past their initial role.

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Applicant Tracking System Keywords

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Hard Skills & Tools

regulatory complianceregulatory documents preparationregulatory guidelines knowledgeclinical trial regulatory affairs

Soft Skills

analytical skillsproblem-solving skillscommunication skillsinterpersonal skills