Key Responsibilities:
Supporting the coordination and management of trial activities
Submitting applications for relevant Regulatory Ethics and Governance permissions to conduct Clinical Trials within the Trust/University.
Identifying screening and assessing the suitability of local patients to take part in research according to specified inclusion/exclusion criteria.
Providing specialist information to patients about taking part in Clinical Trials including the risks and benefits of participation in specific protocols. Initiating and facilitating the process of gaining their informed consent.
Ensuring trial specific investigations and sampling are undertaken as per the Protocol to establish eligibility and to ensure safe entry into trials.
Maintaining accurate documentation in an auditable format and accurately record data as required by each project.
Identifying barriers to recruitment and performance communicating these to the wider team and help facilitate their resolution.
Ensuring all activities undertaken meet the standards set out in the Principles of Good Clinical Practice and National Research Governance Framework for Health & Social Care (DH 2005).
Actively participate in team meetings including research fellows research nurses and department consultants and University staff.
Promote a culture of academic excellence through peer-peer learning and education sessions and journal club
Identifying barriers to recruitment and performance communicating these to the wider team and help facilitate their resolution.
Qualifications :
Qualifications
Full GMC registration with a licence to practice
Good Clinical Practice
Experience
Prior NHS experience in a medical specialty
Prior engagement with research
Development of documents for regulatory approval submission
Clinical Skills
Understanding of clinical risk management
Knowledge
Able to demonstrate appropriate level of clinical knowledge
Knowledge and use of evidence based practice
IT skills
Effective confident presentation ability
Other
The ability to interact well intellectually and personally with colleagues students and patients
Ability to motivate others and engage different staff in activities
Self-motivation initiative and the ability to work both independently and as part of a busy team
Evidence of prioritising and organisational skills and the ability to meet tight deadlines
Excellent written and verbal communication skills including presentation and report writing skills
Good attention to detail
Evidence of participation in audit
Publications
Prizes and honours
Logical thinking problem solving and decision making
Additional Information :
We welcome the unique contributions that you can bring in terms of your education opinions culture ethnicity race sex gender identity and expression nation of origin age languages spoken veterans status colour religion disability sexual orientation and beliefs.
For more information please see our People and OD Strategy 2026
Remote Work :
No
Employment Type :
Full-time
Clinical Research Fellow • Portsmouth, England, UK
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