Senior Clinical Data Manager

📋 Description

• Supervise, direct, manage, and offer technical expertise for the assigned projects to guarantee they are executed efficiently, accurately, and promptly, meeting the Sponsor’s expectations.

• Deliver fully independent and self-sufficient leadership in data management services (initiation, execution, and closure) across various complex global projects/programs.

• Prepare documentation for data management trials (DMP, Database Specifications, Edit check specifications, CCGs, DTAs).

• Ensure that effective User Acceptance Testing (UAT) is conducted.

• Draft specifications for external vendor reconciliation for programming reconciliation outputs (e.g., Serious Adverse Events, IRT, Central Laboratory).

• Supervise activities related to data cleaning.

• Monitor project scope, budgets, and risks, notifying DM Management of any issues.

⛳️ Requirements

• Bachelor’s degree or higher in biomedical sciences, life sciences, computer science, or a related field — or equivalent relevant experience.

• Minimum of 5 years of experience in clinical data management or a similar role within the pharmaceutical, biotechnology, or medical device sectors.

• Strong understanding of data management best practices and technologies as they pertain to clinical trials.

• Solid comprehension of the clinical trial process and related protocol documents (protocols, statistical analysis plans, CRFs, study reports) and processes.

🏝️ Benefits

• Competitive salary

• Flexible working hours

• Professional development opportunities

• Wellness programs