Principal Clinical Data Manager - Late Phase

Principal Clinical Data Manager - Late Phase

13 oct
|
Labcorp Drug Development
|
España

13 oct

Labcorp Drug Development

España

Description



- You will be permanently employed by Labcorp Drug Development working in our Clinical Development Services (CDS) division working across multiple Sponsors and multiple therapeutic areas in Phases IIb to IV.

- Office based or home based anywhere in Europe or South Africa.

- You must have previous experience of working in a lead clinical data management role within clinical research.

- Candidates must be fluent in English language (both verbal and written).



Join our growing team and discover your extraordinary potential by working as a Principal Data Manager within our Global Clinical Development department.



As Principal Data Manager, you will:









- Lead multiple studies and take responsibility for the development of the project documentation, system set-up, data entry and data validation.

- Assign processes to junior staff.

- Assume responsibility for all Data Management activities (from study start up to database lock) according to client expectations.

- Work with leadership team, providing guidance, mentoring, training to the Data Management team.

- Join bid defenses, capabilities presentations and other client engagements regarding budget, scope or DM processes.

- Support budget development process for DM opportunities.



Education/Qualifications:



- University/college degree (life science, pharmacy or related subject preferred), or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing certification, medical or laboratory technology).

- Additional relevant work experience will be considered in lieu of formal qualifications.



Experience:



- Extensive work experience in data management, including direct sponsor management and technical mentoring experience.

- Proven ability to lead by example on project strategies and achievement of department goals, objectives and initiatives to encourage team members to seek solutions.

- Demonstrated skill for technical management of staff.

- Financial management of gross revenues in excess of $250K per year.

- In depth knowledge of clinical trial process and data management, clinical operations, biometrics, quality management, and systems applications to support operations.

- Experience representing DM in bid defense meetings, providing innovative solutions.

- Working knowledge of the relationship and regulatory obligation of the CRO industry with pharmaceutical / biotechnological companies.

- Ability to lead by example teams on project strategies and achievement of department goals, objectives, and initiatives and to encourage team members to seek solutions.

- Demonstrated managerial and interpersonal skills.



MORE INFORMATION AVAILABLE ON REQUEST



For a confidential discussion about this opportunity, please phone Antony McAteer on +44 (0) 7800 913 717. To apply, please click on the APPLY button.



Keywords:



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