Department: Global Development Operations Department
In this role you will:
- Participate in study teams and all related meetings for assigned protocols
- Prepare documents and ensure tools are arranged to allow for data capture and data cleaning
- Ensure delivery of a clean database
- Run and oversee a project or set of studies within a project under supervision of a higher level data manager, which may include outsourcing and CRO oversight for studies for which Data Management activities are done by a CRO
- Instruct, communicate and coach others on data management procedures (lower level data managers, but also providing training to and creating guidelines for monitors and site staff/ investigators)
- Ensure compliance with EMEA, FDA and ICH regulations and policies, including validation deliverables
Your personal qualifications:
- BS/BA degree in a biological science, health-related, or computer science field.
- 7-10 years related experience in pharmaceutical, clinical research or health services industry with at least 4 years of experience with Data Management in the pharmaceutical industry
- Demonstrated knowledge of medical terminology, personal computers, database structures and database management software
- Problem solving attitude and analytical skills
- Capable to work in multidisciplinary and international teams
- Excellent communication, planning & organizing skills
- Experience in working with EDC/ePRO tools
For more information, please contact Priya Mukherjee at CK Clinical on 01438 743 047 or email pmukherjee@ckclinical.co.uk.
