About the facility
SCRI is the first UK trials unit outside of the NHS that has the ability to offer new anti-cancer drugs in clinical trials. As a dedicated trials unit, we are focused on fast study set-ups to offer patients’ rapid access to new investigational drug therapies. Most importantly we are open for both private and NHS patients.
Sarah Cannon Research Institute UK aims to provide precision medicine for cancer patients through the development of targeted therapies that are not only directed towards the cancer cell, but a specific alteration within the cancer cell.
Job Description
As the Data Entry Associate, you will provide support for SCRI UK’s Drug Development Unit (DDU) through the completion of data entry using various Electronic Data Capture (EDC) systems and resolution of data queries.
Salary: Up to £25,000 (Dependent on candidate experience)
Duties & Responsibilities
- Assist with clinical trial eCRF/EDC data entry using clinical data management tools eg: Medidata RAVE, Inform
- Perform- advanced reviews of Case Report forms and electronic Case Report forms
- Resolve discrepancies and reduce data queries by actively reviewing source documents
- Facilitate monitoring visits through data query resolution and data entry and discussion with monitors to meet data entry requirements
- Assist with uploading of clinical trial data eg, scan CDs to Sponsor/CRO secure websites
- To understand the relevant study specific protocol items, identify and bring to the attention of the SCRUK DDU staff study non-compliance that becomes apparent in the process of carrying out their duties.
- Perform ad hoc duties/projects as directed
- To gain a full understanding of the relevant SCRI UK SOPs
- Maintain awareness of HCA policy and procedures relating to the post holder’s role
- Maintain up to date mandatory training and attend other training as relevant to the position.
Skills and Experience
- Preferably degree educated in a biological science or related discipline
- Practical experience using clinical data management tools. Candidates MUST have experience using Medidata RAVE and Inform
- Effective oral and written communication skills
- Knowledge and experience with clinical data and ICH Good Clinical Practices
- Strong attention to detail
- Good organisational, planning and time management skills
About the Individual
The successful candidate will have excellent interpersonal skills, using their strong communication skills to liaise effectively with consultants, colleagues, medical secretaries. They must have strong Data skills and have exposure to both Medidata Rave and Inform.
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About HCA
HCA (Hospital Corporation of America) operates more than 160 acute care, psychiatric, and rehabilitation hospitals in the US and…
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