Start Date
Immediate
Expiry Date
15 Sep, 25
Salary
30570.0
Posted On
15 Jun, 25
Experience
0 year(s) or above
Remote Job
Yes
Telecommute
Yes
Sponsor Visa
No
Skills
Good communication skills
Industry
Pharmaceuticals
Please see the attached Job Description and Person Specification. The post-holder will be responsible for the entry of all allocated commercial and not commercial trial related data into the relevant electronic and paper data capture systems in compliance with the study protocol. The maintenance of accurate and comprehensive records is an essential aspect of this post. The post-holder will work within a research team and work closely with the research nurses, research coordinator and wider research team to manage the Case Report Forms data entry, to liaise with clinical trials units, prepare for audit inspections, to ensure compliance with Research Governance, create source data worksheets and assist with the creation of study specific patient pathways.
As part of the team you will have the opportunity for personal and professional development and ongoing education with access to the Kent, Surrey and Sussex Clinical Research Network. Potential candidates should be able to demonstrate: A good understanding of data collection or clinical audit Good interpersonal and communication skills. For further details / informal visits contact: Louisa Zouita : l.zouita@nhs.net Tel No 01483 571122 ext 4515/349
Please refer the Job description for details