{"id":172685,"date":"2026-04-05T05:44:41","date_gmt":"2026-04-05T05:44:41","guid":{"rendered":"https:\/\/www.whitehattoolbox.com\/jobs\/were-hiring-clinical-research-coordinator\/"},"modified":"2026-04-05T05:44:41","modified_gmt":"2026-04-05T05:44:41","slug":"were-hiring-clinical-research-coordinator","status":"publish","type":"post","link":"https:\/\/www.whitehattoolbox.com\/jobs\/were-hiring-clinical-research-coordinator\/","title":{"rendered":"We\u2019re Hiring Clinical Research Coordinator"},"content":{"rendered":"

Pier Health Group Research Team were established in 2022 and are designated as the NIHR North Somerset Clinical Research Delivery Centre (Primary Care), part of the national network of CRDCs across the UK.<\/span>We are expanding our research team and have an opening for a Clinical Research Coordinator to join our dynamic PCN research team on a full-time basis.<\/span>Main duties of the job<\/b><\/span>As a Clinical Research Coordinator, you will work within a multi-professional team to organise and support the delivery of multiple studies for the local population. You will develop skills across the full lifecycle of research studies, act as a key liaison with study teams and monitors and be supported by a Research Administrator.<\/span>Joining our team means being part of a supportive and collaborative environment that values your expertise and contributions. We foster a culture of learning and innovation and provide ongoing training and mentorship to empower you to reach your full potential.<\/span>About us<\/b><\/span>Founded in 2019, Pier Health Group is committed to delivering top-quality healthcare to over 100,000 patients across Weston-Super-Mare, Worle, and surrounding villages. Our goal is to provide consistent, high-quality primary care across all our practices, enhance patient outcomes, and improve the working lives of our staff. As both a Super-partnership and a Primary Care Network, we are uniquely positioned to drive transformative care in our community.<\/span>Details<\/b><\/span>Date posted<\/span>02 April 2026<\/span>Pay scheme<\/span>Other<\/b><\/span>Salary<\/b><\/span>Depending on experience<\/span>Contract<\/span>Permanent<\/span>Working pattern<\/span>Full-time<\/span>Reference number<\/span>A3508-26-0008<\/span>Job locations<\/span>168 Parklands Medical Group<\/span>Anson Road<\/span>Weston Super Mare<\/span>BS24 7PS<\/span>Job description<\/b><\/span>Job responsibilities<\/b><\/span>We are seeking a highly motivated and detail-oriented Clinical Research Coordinator to join our multi-professional team, focusing on both active participation in research studies and providing essential administrative support. This dual-role position is designed for an individual who can seamlessly balance hands-on involvement in research activities with the efficient management of study delivery. The ideal candidate will possess strong organisational and communication skills, along with a proactive approach to ensuring the smooth operation of research projects within our primary care research team.<\/span>1. Research Involvement<\/span>Collaborate and support research team members to ensure seamless execution of study protocols and delivery of delegated duties.<\/span>Conduct population health searches and identify suitable cohorts of potential recruits for current studies.<\/span>Actively contribute to research studies by providing engagement and support to participants, assisting in data collection, and study tasks under the guidance of the research team or as delegated by the Principal Investigator.<\/span>Manage site equipment, maintenance, calibration and capacity for study delivery.<\/span>Create and utilise research tools for studies such as patient tracker, visit plans, participant activity and travel expenses.<\/span>Support clinical team members with preparations for clinics and documentation including consumables, biological sample processing and despatch.<\/span>Arrange and support vendor platform access for team members.<\/span>Manage financial activities associated with all studies.<\/span>2. Administrative Support<\/span>Provide comprehensive administrative support for research projects, including scheduling meetings and clinics, booking participants, managing calendars, and coordinating study timelines with the team.<\/span>Maintain accurate and organised documentation of research activities, records and communications, archiving.<\/span>Manage associated logistics for clinics and studies, including consumables.<\/span>Support to Administrative Functions (Backup)<\/span>Documenting SOPs and Notes to Files as required.<\/span>3. Communication and Collaboration<\/span>Be the key point of contact for study teams, questions and queries.<\/span>Facilitate effective communication between Participant, research team members, study teams, clinical research network, NIHR and regulatory bodies.<\/span>Support Clinical Research Associate visits on site, coordinating the site team to aid completion of data queries, adverse event reports, preparations for data locks and sign off, documentation for audit and inspection.<\/span>Engage with website, social media and Patient Representatives to support trial participation, site visibility and share news of research studies.<\/span>Participate in meetings to forge new collaborations and opportunities which will attract more research studies for the local population.<\/span>Compile monthly reports as required and update study activity on various platforms.<\/span>4. Compliance<\/span>Monitor and maintain compliance by the team with study protocols and regulatory guidelines throughout the research process.<\/span>Support the collection, verification, security and monitoring of trial data, ensuring accuracy, completeness, and adherence to sponsor and regulatory requirements throughout the lifecycle of the trials.<\/span>Collaborate with team members to support data-related activities, including monitoring checks (e.g. temperature monitoring), policies, protocols, communication tools to support study delivery.<\/span>Regularly review findings from site audits to improve SOPs, conducting annual reviews of SOPs, forms etc.,<\/span>Manage acceptance, implementation and communication of Protocols and subsequent Amendments<\/span>Manage training, Delegation Logs and staff records for all studies and site processes.<\/span>5. Additional Responsibilities<\/span>Participate in training, development, and professional activities to maintain up-to-date knowledge of clinical trial regulations and best practices.<\/span>Provide expert support to the research team to ensure high-quality trial delivery and positive participant experience. Job description<\/span>Job responsibilities<\/b><\/span>We are seeking a highly motivated and detail-oriented Clinical Research Coordinator to join our multi-professional team, focusing on both active participation in research studies and providing essential administrative support. This dual-role position is designed for an individual who can seamlessly balance hands-on involvement in research activities with the efficient management of study delivery. The ideal candidate will possess strong organisational and communication skills, along with a proactive approach to ensuring the smooth operation of research projects within our primary care research team.<\/span>1. Research Involvement<\/span>Collaborate and support research team members to ensure seamless execution of study protocols and delivery of delegated duties.<\/span>Conduct population health searches and identify suitable cohorts of potential recruits for current studies.<\/span>Actively contribute to research studies by providing engagement and support to participants, assisting in data collection, and study tasks under the guidance of the research team or as delegated by the Principal Investigator.<\/span>Manage site equipment, maintenance, calibration and capacity for study delivery.<\/span>Create and utilise research tools for studies such as patient tracker, visit plans, participant activity and travel expenses.<\/span>Support clinical team members with preparations for clinics and documentation including consumables, biological sample processing and despatch.<\/span>Arrange and support vendor platform access for team members.<\/span>Manage financial activities associated with all studies.<\/span>2. Administrative Support<\/span>Provide comprehensive administrative support for research projects, including scheduling meetings and clinics, booking participants, managing calendars, and coordinating study timelines with the team.<\/span>Maintain accurate and organised documentation of research activities, records and communications, archiving.<\/span>Manage associated logistics for clinics and studies, including consumables.<\/span>Support to Administrative Functions (Backup)<\/span>Documenting SOPs and Notes to Files as required.<\/span>3. Communication and Collaboration<\/span>Be the key point of contact for study teams, questions and queries.<\/span>Facilitate effective communication between Participant, research team members, study teams, clinical research network, NIHR and regulatory bodies.<\/span>Support Clinical Research Associate visits on site, coordinating the site team to aid completion of data queries, adverse event reports, preparations for data locks and sign off, documentation for audit and inspection.<\/span>Engage with website, social media and Patient Representatives to support trial participation, site visibility and share news of research studies.<\/span>Participate in meetings to forge new collaborations and opportunities which will attract more research studies for the local population.<\/span>Compile monthly reports as required and update study activity on various platforms.<\/span>4. Compliance<\/span>Monitor and maintain compliance by the team with study protocols and regulatory guidelines throughout the research process.<\/span>Support the collection, verification, security and monitoring of trial data, ensuring accuracy, completeness, and adherence to sponsor and regulatory requirements throughout the lifecycle of the trials.<\/span>Collaborate with team members to support data-related activities, including monitoring checks (e.g. temperature monitoring), policies, protocols, communication tools to support study delivery.<\/span>Regularly review findings from site audits to improve SOPs, conducting annual reviews of SOPs, forms etc.,<\/span>Manage acceptance, implementation and communication of Protocols and subsequent Amendments<\/span>Manage training, Delegation Logs and staff records for all studies and site processes.<\/span>5. Additional Responsibilities<\/span>Participate in training, development, and professional activities to maintain up-to-date knowledge of clinical trial regulations and best practices.<\/span>Provide expert support to the research team to ensure high-quality trial delivery and positive participant experience.<\/span>Person Specification<\/b><\/span>Experience<\/b><\/span>Essential<\/b><\/p>\n