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Clinical Data Manager Opportunity

Clinical Data Manager Opportunity

Job Title: Clinical Data Manager Opportunity
Contract Type: Permanent
Location: Horsham
Industry:
Salary: £35000 per annum
Start Date: 2018-06-22
Reference: 15916a BT
Contact Name: Brian Tappy
Contact Email: pharma.jobs@nextphaserecruitment.com
Job Published: June 22, 2018 10:39

Job Description

To be based in Horsham, West Sussex; as an experienced Clinical Data Manager or Data Coordinator you will have an excellent insight into the process and procedures associated with running clinical trials. This is a great opportunity to utilise your skills to develop a career in Clinical Supply Chain Management. We are sure you will appreciate how vital the supply chain is to the success of any study. Central to all clinical trials is ensuring the correct doses are available for the correct patients and that they are transported under the correct conditions. Without a robust supply chain there would be no clinical trial be it a single center phase 1 or a global phase 3 study.

If you would be interested in exploring a career change within clinical trials, with full training, we would welcome an application from you.

The Company
The company is the global market leader and innovator in the provision of clinical supply chain solutions meeting the requirements of studies across the world. As clinical trials require increasingly complex supply chain support, the company’s integrated solutions provide the global presence and flexibility to integrate into clients own operational and quality processes. The company has operations in across the globe backed by a global distribution infrastructure.

The Role
Based on your clinical trial expertise this role is to join the Clinical Supply Chain Optimisation team as a Clinical Supply Chain Manager at Associate level. The role focuses on supporting external clients and internal Clinical Supply Chain Managers in translating study needs into supply chain strategies. This includes the interpretation of protocols and client’s operating procedures that will be successfully interpreted into robust plans. You will assist in developing processes and procedures ensuring supply availability which will be achieved by forecasting, scheduling, operational coordination and risk management. You will have the ability to work with cross-functional teams for study management activities including internal Project Management colleagues and external CROs, IxRS providers, client clinical supply teams and client clinical operations teams.

Based on your clinical trial experience full training and mentoring will be provided with an ongoing commitment to your development and a clear, structured career path for future progression.    

Benefits
- Highly competitive salary to £35,000
- Full training in Clinical Supply Chains based on clinical trial expertise
- On going development and clear, structured career path for progression
- Contributory pension scheme
- Bonus scheme
- Private health cover
- Childcare vouchers

Experience
The successful candidate will have a good understanding of clinical trial processes and procedures including regulatory standards. You could have gained your expertise working as a Clinical Data Manager or Clinical Data Associate plus this could suit a Clinical Trial Administrator, Clinical Trial Associate, Clinical Research Coordinator, Clinical Research Associate, IxRS Project Coordination, Clinical Supplies Pharmacy Technician or other role with broad clinical trial exposure. This experience could have been gained in a pharmaceutical / sponsor, service provider / CRO or NHS environment.