Clinical Data Manager II/III

• University degree (bioengineering, life science or related subject preferred), or certification in a related allied health profession from an appropriately accredited institution
• Fluency in English
• Minimum 2 years of experience in effective clinical data management practices
• Excellent knowledge of MS Excel
• Ability to analyze information and draw conclusions, initiate appropriate solutions
• Independence in planning activities, resources and time to achieve the set goals and objectives
• Communication skills, teamwork and ability to contact with the client in order to learn about and solve problems

Nice to have:

• Programming skills (R, SAS)

• Taking the role of Lead Data Manager for allocated projects
• Accountability for all DM deliverables per the established timeline; providing instruction to DM study team and reviewing their study team’s output while adjusting resource allocations within the project accordingly
• Overseeing all allocated projects are carried out in strict accordance with the relevant protocols, global harmonized SOPs, and the specified standards of GCP
• Working with the Project Manager to build timelines to meet contracted milestones by communicating with leads in different disciplines and the project team
• Maintaining awareness of other Biometrics functional group deliverables to be able to support risk and mitigation strategies
• Ensuring service and quality agreed upon specifications per the DMP and scope of work
• Performing quality control in all aspects of the study
• Reconciling the clinical database against safety data, laboratory data or any other third party data as appropriate, utilising local laboratory systems and batch data load facilities where appropriate