Data Surveillance Analyst - based in Lithuania, Romania, South Africa

Data Surveillance Analyst - based in Lithuania, Romania, South Africa

Join to apply for the Data Surveillance Analyst - based in Lithuania, Romania, South Africa role at Parexel .

Parexel is currently seeking a Data Surveillance Analyst to join us in either Lithuania, Romania, or South Africa.

Picture Yourself At Parexel :

The Data Surveillance Analyst (DSA) is responsible for analyzing scientific and operational data to support the Data Surveillance process and reviewing project‑specific Quality Tolerance Limits. They assist in developing Data Surveillance Plans (DSPs) and conduct defined project reviews. The DSA also attends internal and external Data Surveillance meetings, where they present relevant findings to the project team.

What You'll Do At Parexel :

Data Surveillance Plan Development and Technology Configuration :

• Support cross‑functional study team with expertise of Data Surveillance Process and supporting technologies.
• Support the development of a robust Data Surveillance Plan, including Key Risk Indicators, Quality Tolerance Limits.
• Configure and Maintain Data Surveillance technologies (e.g., Clue Points Central Monitoring Platform).
• Review relevant data via the scoped technologies, identifying findings related to trends, outliers, emerging risks, and systemic issues.
• Document findings from Data Surveillance review.
• Provide feedback and work with Technology teams to identify potential solutions that match the business and technology strategy.
• Perform presentations explaining identified findings to internal cross‑functional study team and client team.
• Apply working knowledge and judgment to identify and evaluate potential data quality trend, outliers, and emergent issues. Determine and implement appropriate follow‑up action with the input of other / relevant parties and / or guidance provided, if applicable.
• Actively participate in external or internal meetings and audits & regulatory inspections as required.
• Recognize impact of study non‑compliance / issues / delays / data quality signals and communicate / promptly elevate to FL any site and / or study issues that require immediate action.
• Maintain a working knowledge of and ensure compliance with applicable ICH‑GCP Guidelines, international and local regulations, Parexel SOPs, other Parexel / Sponsor training requirements and study.
• Collaborate with DS Team Members to correlate findings from various sources.
• Support Project Leads with DS Review meeting, driving reviews and decisions as needed and agreeing on actions.
• Engage DS Team to compile signals / actions into client‑ready list.
• Support documentation of actions in Clue Points Issue Management system.
• Complete, share, and file Central Monitoring Report.

Requirements :

A Little About Us

Highly qualified and dynamic team. Multinational working environment. Smooth induction and training program. We offer competitive financial packages, training, and development. Expect exciting professional challenges but with a healthy work / life balance. We value your welfare just as highly as that of our patients.

Parexel has a fully flexible work arrangement – you can be fully home based. But if you live close to our office and you want to use it, you are always welcome, and we will keep the desk ready for you!

Seniority level

Associate

Employment type

Full‑time

Job function

Research

Industries

Pharmaceutical Manufacturing, Biotechnology Research, and Hospitals and Health Care

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