- You will contribute to the success of our clinical programs by analyzing data and implementing validation protocols that support regulatory compliance and data quality
- What You Will Be Doing
- Conducting data validation and quality assurance checks to ensure the integrity of clinical trial data
- Collaborating with cross-functional teams to define validation requirements and develop validation plans
- Identifying and resolving data discrepancies, documenting findings, and recommending corrective actions
- Supporting the development and maintenance of validation documentation, including protocols and reports
- Staying updated on industry best practices and regulatory requirements related to data validation
Your Profile
- Degree in life sciences, statistics, computer science, or a related field
- Minimum 2 to 5 years of experience in clinical data management, validation,
or a related role within a clinical research workplace
- Must experience in testing of SAS listing, edit check testing/UAT testing
- Strong analytical skills and attention to detail in data analysis and validation processes
- Working functional knowledge level of EDC Clinical Systems
- Ability to apply working knowledge of Testing EDC Clinical Systems developed through education or past experiences
- Cross reference protocol and be aware of best practices
- Other responsibilities may be assigned as required
- Ability and willingness to be a contributing team member
- Minimal supervisory responsibilities; developing technical acumen and applying acquired knowledge to delivery requirements