Clinical Trials Coordinator

The Clinical Trials Coordinator utilises clinical expertise,experience and knowledge to promote and manage the Pinfold Medical Practice clinical trials team to secure and deliver clinical research projects and studies. This includes working in collaboration with the Primary Investigator to review feasibilities and to drive recruitment into studies.

Key responsibilities and duties
:

• Work with the Clinical Research Network and Pharmaceutical Companies to identify potential studies and research projects
• Help with marketing the Pinfold Trials Team in searching for new work
• Work with the Primary Investigator to review feasibilities of clinical studies
• Drive recruitment of potential participants identified through the clinical reporting process and other internal referrals
• Coordinate all aspects of the set-up and day-to-day conduct of clinical trials in accordance with ICH GCP and other relevant regulatory guidelines
• Review and negotiate Clinical trials Agreements and Financial Agreements
• Review of data and files in preparation for and prior to audits or site inspections
• Lead engagement with the CRDC on clinical trials and associated research initiatives, serving as the primary representative and point of contact
• Manage the activities of a small research team
• Being comfortable with face-to-face and telephone communication with patients
• Understanding of active protocols and tracking changes and amendments
• Competency with basic lab procedures and biological sample handling

Pinfold Medical Practice have an opportunity for you to be part of a developing research organisation in Primary Care. We have a long history of research activity and are now part of the Leicestershire, Northampton and Rutland CRDC. Also leading local GP practices in the Charnwood Primary Care Research Collaborative, we are building a research organisation capable of delivering trials s is your chance to be part of this exciting journey.

We offer:

• NHSpension
• Freeon-site parking
• A supportive,friendly and welcoming team environment.

To contribute to all aspects of the planning, conduct and reporting of all clinical trials for Pinfold Medical Practice.

To work on a daily basis with minimal supervision with Research Administrator, Lead GP Partner and Business Manager

Coordinate all aspects of the set-up and day-to-day conduct of clinical trials in accordance with ICH GCP and other relevant regulatory guidelines

To maintain a high standard of patient care in line with NHS/practice policies and protocols and in accordance with the Research Governance Framework.

To ensure that all data is collected and managed effectively and accurately

To contribute to all aspects of the planning, conduct and reporting of all clinical trials within the research speciality

Knowledge of clinical research including issues on ethics, law, drug development and management in clinical issues

Maintaining overall standard of care for patients at all times

Educational and developmental role

Ability to give advice on the organisation and management of research in progress

Liaison with sponsor companies and multi-disciplinary research teams

Key responsibilities

Work with the Clinical Research Network and Pharmaceutical Companies to identify potential studies and research projects

Lead engagement with the CRDC on clinical trials and associated research initiatives, serving as the primary representative and point of contact

Help with marketing the Pinfold Trials Team in searching for new work

Work with the Primary Investigator to review feasibilities of clinical studies

Drive recruitment of potential participants identified through the clinical reporting process and other internal referrals

Review and negotiate Clinical trials Agreements and Financial Agreements

Review of data and files in preparation for and prior to audits or site inspections

Manage the activities of a small research team

Being comfortable with face to face and telephone communication with patients

Understanding of active protocols and tracking changes and amendments

Competency with basic lab procedures and biological sample handling.

Provide ongoing advice and information to…