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Lead Data Manager, Abingdon



Abingdon, United Kingdom 

Job Category:



€40,000.00 - €50,000.00

EU work permit required:


Job Reference:

mc 23427_1531296559

Job Views:




Expiry Date:


Job Description:

An excellent opportunity has arisen to join a leading CRO company as a Lead Data Manager.

The scope of responsibilities will include:

Primary communication point for vendors, project teams and company departments with regard to clinical data management.

Data Management

Coordination of data management activities within clinical projects
Primary responsibility for clinical data management activities within clinical projects, including, but not limited to:
• Study documents review
• Data Management Plan and other project-specific guidelines and instructions development and review
• Co-ordinate/perform user acceptance testing
• Development of Data Validation Plan/Edit Check Specifications
• Data entry coordination and supervision, feedback to data entry personnel regarding quality of data entry and other data entry issues
• Data validation, including automatic and manual data inspections, data discrepancies/deficiencies review and resolution, query generation and resolution, feedback to clinical trial teams regarding the quality of data
• Non-CRF electronic data handling (receiving, archiving, loading into study database, review and resolution of reconciliation issues, feedback to vendors regarding the quality of data and other issues)
• Database edits (paper CRF studies)
• Manual CRF review (non-medical checks)
• Clinical database lock
• Coordination and supervision of processing, dispatch and archiving of CRFs/queries

Input into the design of CRFs and other data collection forms; review Case Report Form design for accuracy and adherence to protocol
Development of CRF completion guidelines
Coding medical data with coding dictionaries and coding listings review (Lead DMs with medical/biology background, additional training required)
SAE reconciliation
Electronic data transfer (import/export) specifications review and approval

• College or University degree, life sciences or medical background is a plus
• Prior experience in pharmaceutical/clinical trial industry
• Experience in a professional environment, preferably with clinical or medical data
• Experience in Clinical Data Management systems (Medidata Rave, Oracle InForm, ClinTrial)
• Good command of English, written and spoken
• Proficient user of standard MS Office applications and MS Access
• Strong organizational and time management skills
• Ability to work independently and perform multi-task activities
• Good attention to detail
• Good typing and document management skills

Key People is a specialist international recruitment consultancy with over 25 years’ experience of working within the life sciences, biotech, healthcare and CRO industries. Our experienced and dedicated clinical research related consultants have a long history of success, excellent technical knowledge and a flexible, consultative focussed approach to recruitment.

Please contact Mark Cussens, Clinical Research Recruiter on
Tel: +44 1727 817623 or email: mcussens@keypeople.co.uk
Tel: +41 4350 86620 or email: mark.cussens@keypeopleswitzerland.ch

Key People is a recruitment company with a reputation for providing good value that’s been built up over 20 years.
- We achieve results faster
- Our candidates really are a cut above
- We add greater value
We think it’s because we’re a private company driven by clients, not by shareholders.

For our candidates, we have developed relationships with thousands of clients nationwide and across Europe, who choose to recruit through Key People, so you’ll have a wide choice of opportunities to further your career.

Company Info
Key People
Catherine House
St Albans, United Kingdom
Phone: 441727811634
Web Site: www.keypeople.co.uk
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