Mylene Paumier at CK Clinical is currently recruiting for a Clinical Data Manager for a leading Pharmaceutical organisation in the South-East of the UK.
As a Data Manager, you will help shape a small, growing team in the UK and it will be the perfect environment for your clinical research expertise and your knowledge of EDC. You will be an individual contributor performing complex data management tasks independently and managing external vendors on assigned studies. Besides reviewing clinical study protocols, you will develop eCRFs for new and complex projects, conduct the cross-functional Data Review and develop the Data Management study timeline. Another part of your brief will involve overseeing vendor DM activities, including timeliness and quality of deliverables, and also reviewing statistical tables and listings and Clinical Study Reports, ensuring study compliance with SOPs and regulations.
In addition, you will plan and oversee development of:
- Data Management Plans
- Data Entry Guidelines
- CRF Completion Guidelines
- Data Review Guidelines,
- eCRF help text
- plan, perform and oversee development of specifications for eCRFs, edit checks, electronic data handling, and manual review.
Qualifications and skills:
Interested applicants will hold a degree (OR Equivalent) in a Life Science, Computer Science or other related discipline, and you will have proven experience of working within the Biotechnology/CRO/Pharmaceutical field. You will hold excellent knowledge of Clinical Data Management and EDC (ideally InForm), and have well-developed communication skills to liaise with various stakeholders across the business.
For more information or to apply for this Clinical Data Manager position, please contact Mylene Paumier on 01438 743047 or email firstname.lastname@example.org. Please quote reference CL24392 in all correspondence.