Senior Clinical Trial Regulatory Advisor, Hybrid- or Remote based in Serbia

Senior Clinical Trial Regulatory Advisor, Hybrid- or Remote based in Serbia
Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress.

Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape.

Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to deliver – for one another, our customers, and, most importantly, for those in need.

Discover what your 25,000 future colleagues already know:

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 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 are continuously building the company we all want to work for and our customers want to work with. Why? Because we know that when we bring together smart colleagues from across the world, we can shape the future of healthcare, driving impact for customers and defining the pace of patient progress.

Job Responsibilities

Seeking candidates with specialized regulatory technical and functional expertise, including experience in areas such as Early Access Programs (EAP), In Vitro Diagnostic Regulation (IVDR), Companion Diagnostics (CDx), and other relevant regulatory pathways.
Role Profile
A regulatory delivery professional responsible for translating regulatory strategy into high-quality, compliant, and timely operational execution. This individual ensures that regulatory activities are effectively planned, coordinated, and delivered to support successful study activation and ongoing compliance.
Key Accountabilities

- Ensure submission readiness through the delivery of high-quality, accurate regulatory documentation.

- Develop and maintain realistic regulatory plans, timelines, and assumptions.

- Coordinate timely collection, review, and management of required submission documentation.

- Proactively identify regulatory risks, constraints, and potential impacts to study timelines.

- Align regulatory activities with the broader study activation strategy and timelines.

- Maintain compliance with applicable local, regional, and global regulatory requirements.
Core Capabilities

- Regulatory submission planning and execution

- Strong knowledge of country-specific and regional regulatory requirements

- Project planning, coordination, and document management

- Quality-focused approach with a strong compliance mindset

- Risk identification, assessment, and mitigation

- Effective cross-functional stakeholder communication

- Accurate tracking and management of regulatory data, milestones, and deliverables
Required Experience

- Demonstrated experience preparing, coordinating, or overseeing clinical trial regulatory submissions.

- Experience managing submissions across multiple countries, regions, or regulatory pathways.

- Proven ability to manage submission documentation, dependencies, and critical timelines.

- Experience collaborating with cross-functional study teams, investigative sites, ethics committees, and regulatory authorities.

- Track record of identifying and resolving submission readiness, quality, or compliance issues to ensure successful regulatory outcomes.

Get to know Syneos Health

Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients.

No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health.

http://www.syneoshealth.com

Additional Information

Tasks, duties, and responsibilities as listed in this job description are not exhaustive.  The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description.  The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above.   Further, nothing contained herein should be construed to create an employment contract.  Occasionally, required skills/experiences for jobs are expressed in brief terms.  Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees.  The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.