Sara Bradic
@sarabradic
I manage clinical site contracts and pharmacovigilance case safety processes.
SerbiaWhat I'm looking for
I'm currently supporting Parexel as a Site Contract Associate I, drafting, reviewing, and negotiating clinical study and service agreements while aligning terms with study budgets, protocols, and timelines.
Previously at PrimeVigilance, I managed ICSR triage and follow-up, SAE/SUSAR cases, MedDRA and WHO coding, safety data reporting, and regulatory submissions. I used Oracle Argus and Oasis databases to maintain accurate, compliant safety information and support client reporting.
My background in biochemical engineering, pharmacy, and laboratory work helps me approach clinical and safety documentation with care for compliance, data quality, and patient safety.
I'm fluent in Serbian, English, German, and Croatian, and I bring organized communication, client relationship management, quality checks, and problem-solving to pharmaceutical and clinical research teams.
Experience
Work history, roles, and key accomplishments
Draft, review, and negotiate clinical study and service agreements, ensuring compliance with ICH-GCP and internal policies. Act as liaison between clinical sites and internal teams, managing contract execution and maintaining accurate records.
Education
Degrees, certifications, and relevant coursework
University of Belgrade
Bachelor of Science, Biochemical Engineering
2015 - 2023
Bachelor's degree in Biochemical Engineering from the University of Belgrade, Faculty of Technology and Metallurgy.
Tech stack
Software and tools used professionally
Availability
Location
SerbiaAuthorized to work in
Job categories
Skills
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