Associate Clinical Data Manager

JOB DESCRIPTION:

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 Abbotts quality standards.

What Youll Do

• 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.

What Youll Bring

• Bachelors 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.

What We Offer

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

Required Experience:

Manager

Employment Type : Full-Time
Experience: years
Vacancy: 1