Requirements Summary

Must-have qualifications include a Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, Nursing, or a related discipline, and relevant professional experience in Clinical Data Management or the Clinical Research industry

Benefits

Full Job Description

Role Overview Supports the management and quality of clinical trial data throughout the clinical research lifecycle. Collaborates with cross-functional teams and client stakeholders while contributing to database testing, query management, and database lock activities. What You Will Do Extract, clean, validate, and reconcile clinical trial data from multiple sources to ensure accuracy, consistency, and readiness for regulatory and research objectives. Why It Might Be a Fit Strong attention to detail and knowledge of clinical research standards are essential to maintaining reliable, high-quality trial data. Requirements Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, Nursing, or a related discipline. Relevant professional experience in Clinical Data Management or the Clinical Research industry. Hands-on experience with Clinical Data Management Systems such as Medidata Rave, Veeva, DataLabs, ClinBase, or similar platforms. Strong understanding of clinical data management processes, including data cleaning, validation, query management, reconciliation, and database lock activities. Knowledge of clinical coding dictionaries such as MedDRA and WHODrug. Basic knowledge of SAS and CDISC standards. Good understanding of ICH-GCP guidelines, clinical research regulations, and applicable industry standards. Strong analytical and problem-solving abilities, with a structured approach to identifying and resolving data discrepancies. Exceptional attention to detail and a strong commitment to data quality and accuracy. Excellent written and verbal communication skills, with the ability to collaborate effectively across cross-functional teams. Strong time management and prioritization skills, with the ability to manage multiple activities and deadlines. Ability to work independently while contributing effectively within collaborative study teams. Adaptability and willingness to learn new technologies, systems, and clinical data management processes. Benefits Opportunities to work on clinical research and data management activities with meaningful impact on healthcare and patient outcomes. Exposure to clinical data management systems, regulatory standards, and industry-leading practices. Collaborative environment involving cross-functional study teams and client stakeholders. Opportunities to mentor junior colleagues and contribute to process improvement initiatives. Professional development through exposure to evolving technologies and clinical research processes.

Skills and Technologies