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.