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Syneos Health

Tech Compliance Analyst I

LocationSRB-Belgrade-Hybrid
Work modehybrid
Typefull-time
SeniorityEntry
DepartmentInformation Technology
Company size10,000+ people
PostedDec 11, 2025 · 10mo ago
Verified live2h ago
At a glanceSummarised by Seekless from the posting.
Must have5
Bachelor's Degree in Computer Science or related science field or equivalent
Experience with 21 CFR Part 11 required
Experience in computer systems validation/software development life cycle approaches
Experience in working in a clinical trials environment, including a comprehensive knowledge of GCP regulations guidelines
Effective verbal and written communication
Tech Compliance Analyst I
About the company
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.
Every day we perform better because of how we work together, as one team, each the best at what we do. We bring a wide range of talented experts together across a wide range of business-critical services that support our business. Every role within Corporate is vital to furthering our vision of Shortening the Distance from Lab to Life®.
Discover what our 29,000 employees, across 110 countries already know.
WORK HERE MATTERS EVERYWHERE
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 our Total Self culture – where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people.
•
We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives – we’re able to create a place where everyone feels like they belong.
Job Responsibilities
Core Responsibilities
• Manage and/or coordinate the writing and execution of validation protocols, specifications, change controls and/or scripts related to software, instruments and/or equipment according to the organization’s compliance requirements and industry regulations.
• Provide support for Information Technology’s project portfolio within assigned projects, ensuring that technology solutions are classified in accordance with set standards, implemented to support those standards within agreed upon timelines.
• Coordinate assigned project deliverables with external consultants and suppliers concerning the implementation, validation, support and maintenance to ensure these activities are completed in alignment with standard compliance principles.
• Serve as subject matter expert in specialized project area to support client and regulatory agency audits and inspections for Information Technology activities.
• Lead compliance efforts for any corrective or preventative actions plans supporting assigned Information Technology solutions.
• Execute harmonization of compliance activities to support mergers, acquisitions and internal expansion of the compliance program.
• Act as a compliance resource expert to other groups.
• Assist internal clients with requests and problem resolution, participate in the maintenance of documentation and make recommendations for greater effectiveness in functional area of compliance
• Make recommendations for continued improvement in the area of compliance for Information Technology.
• Perform training in the principles of computerized systems validation for internal personnel.
• Conduct periodic reviews of validation documentation to ensure systems continue to operate in a validated state and perform impact assessments on planned GxP and Business Critical Change Management requests.
• Perform quality reviews of validation deliverables.
Qualifications
• Bachelor’s Degree in Computer Science or related science field or equivalent.
• Experience with 21 CFR Part 11 required
• Experience in computer systems validation/software development life cycle approaches.
• Experience in working in a clinical trials environment, including a comprehensive knowledge of GCP regulations guidelines
• Effective verbal and written communication
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.
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