Open to opportunities

Vanja Parača

@vanjaparaa

Clinical Research Coordinator blending pharmacovigilance and regulatory documentation to drive compliant safety processes.

Serbia

Message

What I'm looking for

I’m looking for a regulated CRO or clinical team where I can own compliant safety documentation, maintain high-quality safety databases, and collaborate cross-functionally—so study timelines stay on track while accuracy and adherence to GVP/SOPs remain non-negotiable.

I’m a life sciences professional and Clinical Research Coordinator with a pharmacovigilance and clinical research background, focused on documentation management, regulatory compliance, and accurate safety data handling. I’ve managed and reviewed clinical safety documentation in compliance with GVP, SOPs, and regulatory requirements, ensuring completeness and timely processing within strict timelines.

In my roles, I maintained and updated safety databases to protect data quality and consistency, tracked case progress and follow-up activities, and prepared structured case narratives and study documentation. I also support cross-functional coordination with clinical, regulatory, and QA teams in fast-paced, compliance-driven settings—bringing the same attention to detail I developed through documentation and data integrity work.

Experience

Work history, roles, and key accomplishments

Sales Representative

Unifarm Medicom

Apr 2025 - Feb 2026 (10 months)

Provided administrative and operational support by managing client communication and order documentation while coordinating workflows with sales, logistics, and internal teams. Ensured timely, accurate processing in line with internal procedures and maintained high-quality documentation and records.

Client Communication Documentation Management Logistics Support

Professional PV Associate

PrimeVigilance

Jan 2024 - Mar 2025 (1 year 2 months)

Managed and reviewed clinical safety documentation to ensure compliance with GVP, SOPs, and regulatory requirements within a CRO environment. Maintained safety databases, tracked case progress and timelines, and prepared structured case narratives while coordinating with clinical, regulatory, and QA teams.

Pharmacovigilance GVP Compliance & Regulatory

Curator Trainee Ornithologist

Natural History Museum in Belgrade

Jul 2022 - Sep 2023 (1 year 2 months)

Supported ornithology collection work by cataloging and preserving rare avian specimens to improve collection accuracy and support research initiatives. Completed editorial proofreading and review tasks to maintain documentation quality within the museum’s ornithology department.

Collection Management Proofreading Editorial Research Support

Intern Ornithologist

Centre for Protection and Research of Birds, Montenegro

Nov 2021 - Jul 2022 (8 months)

Assisted with bird identification, field surveys, and ecological data collection for ornithological research projects. Tracked migratory bird patterns using field observations, supporting data accuracy and regional species conservation planning.

Bird Identification Survey Fielding Migratory Pattern Tracking Data Entry Research Support Survey Data Accuracy