Essential Functions

Gather Study Set up requirements through discussion and communication with relevant stakeholders.

With Minimal guidance - support, overview of validation of new Device integrations.

Oversight & Perform regular Data cleaning activities to ensure clean data with quality and timely deliverables to sponsor.

Ensure that all the deliverables are of expected quality standards and meet customer expectations.

With guidance, ensure service and quality meet agreed upon timelines and deliverables in contract/Scope of Work (SOW).

Support Training of New joiners.

Lead internal study meetings and internal/ sponsor audits and participate in Study Kick off meetings and other sponsor meetings.

Tracks and manages the projects, oversee project progress, identify risks and take corrective action to rectify any errors as recommended as required.

With Guidance manage & oversight the implementation of new technology / database revisions.

Work closely with the programming team for process innovation and automation.

Be compliant to trainings and eSOP reading.

Provide review and expert opinion in developing, revising, and maintaining core operating procedures and working instructions.

Communication with Line Manager, and other team members across functions should be collaborative.

Perform other duties as directed by Line Manager.

Qualifications

Bachelor's Degree In health, clinical, biological or mathematical sciences, or related field with proven experience in Data Management Req

3 -4 years direct Data Management experience, including a minimum of 1 year as a CDM project lead. Pref

English Fluency Spoken and English Advanced

Advanced computer applications like Microsoft excel, word, Inbox etc

Should have Advanced understanding of Drug development lifecycle and Overall Clinical research process Advanced