Posted on 30th December 2025
Expires on 28th February 2026
Negotiable
Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.
Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for.
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 accelerate the delivery of therapies, because we are passionate to change lives.
Discover what our 29,000 employees, across 110 countries already know:
The Regulatory Intelligence Department at Syneos Health impact decision-making at the highest levels. The team translate and refine Syneos Health regulatory intelligence from internal and external sources and combine knowledge from therapy areas and functions to deliver proactive advice outlining risks and new opportunities to the regulatory strategy and operations.
The Senior Consultant, Regulatory Intelligence is an internal facing role that supports keeping the Syneos Health Regulatory Intelligence System current and accurate via regular surveillance and interaction with subject matter experts.
Gather new regulatory information through routine surveillance of agreed regulatory sources.
Reviews surveillance alerts and queries and determines actions to be taken.
Support ad-hoc research requests from the business and gather regulatory information for potentially new topics.
Manage Regulatory Intelligence Network list of functional SMEs.
Interacts with external and internal experts to collect country and region-specific regulatory intelligence.
Conducts searches within commercial Regulatory Intelligence databases to identify regulations and guidelines relevant for clinical regulatory intelligence.
Keeps abreast of regulations, trends, developments, and advances in the global regulatory environment.
Identifies and responds appropriately to issues and problems, providing innovative and effective solutions.
Recommends and implements enhancements of Syneos Health Regulatory Intelligence processes to maintain the Regulatory Intelligence System
Performs other work-related duties as assigned.
BA / BS in life sciences, regulatory intelligence, regulatory affairs, regulatory operations, or related field required or regional equivalent or equivalent combination of education and experience.
Ability to analyze information across multiple sources and manage substantial amounts of details.
Strong research skills required to support routine surveillance activities to detect, monitor, and synthesize complex regulatory information.
Ability to interact with stakeholder from multiple departments at different seniority levels.
Ability to work independently and to understand and conduct detailed instructions.
Strong written and oral communication skills
Excellent problem solving and decision-making skills.
Fluent in speaking, writing, and reading English.
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.
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.