Clinical Data Manager II - Permanent
Pharmaceutical Company based neat Oxford
Broad and challenging leadership role for a capable Lead Clinical Data Manager who has been involved with projects from database design to reporting and worked with global stakeholders to enable prompt analysis and decision making. Our client is an employer of choice, a global pharmaceutical company which is creating a buzz and achieving breaking new ground in medical intervention in key disease areas including oncology, infection, respiratory disease and immunology.
We are only considering candidates who have developed eCRFs and completed UAT testing with RDE vendors and those who have acted as Data Project Lead on R&D studies throughout most parts of the^project life cycle from database design stage to database lock.
This position will suit a candidate who has led data management inputs for clinical studies in at least one Phase. If you have outsourced components to vendors and assessed bids and^managed contract and scope then all the better as this role will focus on studies placed with vendors.
Perform complex data management tasks independently
Develop Data Management study timelines
Review clinical study protocols, and develop eCRFs^for new and complex projects
Management of external vendors
Monitor compliance with SOPs and regulations
Develop study-specific training
Execute User Acceptance Testing (UAT)
Essential Skills & Qualifications Required
Life science degree or equivalent
Thorough knowledge of Clinical Data Management and EDC across project lifecycle in Phase I-III
Project management skills
Excellent communication skills
Software Competence Required: InForm knowledge and application
Employer: Pharmaceutical Company
Hours: Full time
Location: Office Based, M40/A34 access
Data Manager, Coding, Clinical Data Management,RDE, EDC, eCRF, SOPs, Compliance, UAT, Inform
Assigned Consultant:^Matthew Pike at CSL on 01932 228 928
Please fee free to call for a detailed Job Description or additional information