Associate Clinical Data Manager

We are currently looking for an Associate Clinical Data Manager to join our team based in Belgium. In this role, you will be responsible for leading data review and risk-based data quality activities across assigned clinical studies. You will play a key role in ensuring the accuracy, completeness, and integrity of clinical trial data to support regulatory submissions, safety monitoring, scientific publications, and business decisions. You will collaborate closely with cross-functional study teams and contribute to the successful delivery of high-quality clinical research in accordance with Good Clinical Practice (GCP), Good Clinical Data Management Practices (GCDMP), and Abbott's quality standards.

Lead risk-based data management and review activities for assigned clinical studies, ensuring the quality, integrity, and reliability of study data. Partner with cross-functional teams during protocol development to identify critical study data and establish effective data collection and management strategies. Drive the development and maintenance of study data management deliverables, including Case Report Forms (CRFs), edit checks, data listings, and clinical database specifications. Review and analyze clinical trial data, managing data discrepancies, query resolution, and the identification and escalation of significant data quality issues. Collaborate with Clinical Operations, Clinical Science, Safety, Biometrics, Project Management, and study sites to proactively resolve data-related risks and support study execution. Manage study progress toward data cleaning, database freeze, and database lock milestones to support regulatory submissions and other key business objectives. Oversee study-wide data quality activities and ensure adherence to GCP, GCDMP, regulatory requirements, and internal standards. Act as a trusted data management partner, providing insights and recommendations that support high-quality study conduct and successful clinical outcomes.

Bachelor's degree in Life Sciences, Healthcare, Data Management, or a related field, or an equivalent combination of education and experience. Experience in Clinical Data Management within clinical research, clinical operations, healthcare, or a related environment. Knowledge of Good Clinical Practice (GCP), clinical trial processes, and data quality principles. Experience working with electronic data capture (EDC) systems and clinical databases. Strong analytical and problem-solving skills, with the ability to interpret complex clinical data and identify trends or risks. Excellent organizational skills with the ability to manage multiple priorities and deliverables in a fast-paced environment. Strong written and verbal communication skills, with the ability to collaborate effectively across cross-functional and global teams. Experience supporting medical device clinical studies and familiarity with risk-based quality management practices is preferred.

Abbott offers a challenging position in an international and dynamic environment where you can develop both professionally and personally. We provide competitive compensation and benefits, ongoing learning opportunities, and the opportunity to make a meaningful impact on patients' lives through innovative healthcare technologies. The base pay for this position is N/A In specific locations, the pay range may vary from the range posted.       JOB FAMILY: Clinical Affairs / Statistics DIVISION: MD Medical Devices LOCATION: Belgium : Building Figueras Da Vinci Laan, 11 Box F1 ADDITIONAL LOCATIONS: WORK SHIFT: Standard TRAVEL: Not specified MEDICAL SURVEILLANCE: Not Applicable SIGNIFICANT WORK ACTIVITIES: Not Applicable