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Dear AllStat,
CK Clinical is recruiting for a Snr Data Manager to join a Leading Pharmaceutical Company in Switzerland on a Permanent basis.
As Snr Data Manager you will have the following responsibilities:
Provide timely and professional ongoing management of project & clinical trial data by identifying and resolving errors and inconsistencies in eCRF
data to ensure consistently high standard database(s) with respect to cost, quality and timelines.
1. Serve as Project Data Manager for large projects or multiple smaller projects providing professional Data Management input on ICT(s).
2. Responsible for ensuring consistency of protocols, Validation and Analysis Plans (VAPs) & Project eCRFs for all trials within assigned projects.
3. Business understanding of the compound profile (CDP/TPP) to identify and assist in successful application of data management processes.
4. Respond to Health Authority requests for data management issues.
5. Support and assist Assistant Data Managers and other Data Managers for allocated trials within assigned project(s).
6. Provide input, review, and maintenance of global working practices and standards.
7. Contribute to the development of the Data Management organization through his/her leadership role within the DM Group.
8. Track and report status and progress of data management for allocated trials and be proactive to ensure smooth and successful timely locking
of databases. Ensure appropriate the Organisation tracking systems are up to date and accurate.
9. Lead and support clinical & non-clinical special projects.
10. May deputize for Data Management Group Head and assist in coaching, training and mentoring of Data Management staff
As Snr Data Manager, you will have the following education, skills and experience:
University or college degree in life science, computer science, pharmacy, nursing or equivalent relevant degree. Fluent English (oral and written).
1. experience in drug development, with experience in Data Management activities. 2. Project team leadership experience required. 3. Good technical and problem solving skills. 4. Thorough understanding of clinical trial methodology, GCP and medical terminology.
5. Ability to work independently, under pressure, demonstrating initiative and flexibility. 6. Attention to detail and quality focused. 7. Good organizational, planning and project management skills. 8. Good interpersonal and communication skills and ability
to operate effectively in an international environment. 9. Good negotiation skills. 10. Thorough understanding of physiology, pharmacology, clinical study objectives and the drug development process. 11. Ability to mentor, coach within Data Management and
cross functionally, and train internal and external partners
For more information or to apply for this position, please contact Mylene Paumier on
+44 (0)207 470 5672 or email:
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Best regards,
Mylene Paumier CertRP
Senior European Recruitment Consultant
CK Clinical Limited
Crown House
72, Hammersmith Road
London
W14 8TH
DD: +44 (0)207 470 5672
Tel: +44 (0)207 470 5670
We are part of CKA Group – Winner of Kelly Services 2012 Global Supplier Excellence Award
CK Clinical, CK IT, CK Regulatory and CK Science are trade names of CK Associates Limited
Registered in England No 2611749
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