study coordinator jobs in Cambridgeshire

You will act as the primary contact for study management tasks, providing strategic leadership and ensuring high-quality delivery in line with ethical and regulatory standards.

You will take pride in producing exceptionally high-quality work and will relish the opportunity to build successful relationships with clients, as well as internal colleagues.

You will be part of creating presentations for team meetings to ensure everyone is up to date with the latest.

Job Type: Full-time, non-exempt Reports to: Executive Director, Head of Site Operations Join Us at Civia Health At Civia Health, our Clinical Research Coordinators are essential to deliver trials that are efficient, ethical, and patient-centered. We’re seeking an organized and motivated CRC who thrives in a fast-paced, collaborative research setting. You’ll be the primary point of contact for...

You will work closely with the Senior Team Leader, CCIO and the Design Authority, requiring in-depth technical knowledge of both the Epic application and the business and clinical processes across the organization.

You will manage a complex caseload and deliver expert physiotherapy interventions, applying advanced clinical judgement and initiative to guide rehabilitation decisions. The complexity of care within our regional Major Trauma Centre provides a stimulating setting with scope for innovation and service development.

You must have appropriate UK professional registration.

Patient Experience Booking Coordinator The Patient Experience Booking Coordinator provides professional administrative support within Outpatients, ensuring a high standard of service to patients, relatives, and colleagues. The role supports interpreting, accessibility, and main reception services, helping to deliver an efficient and positive patient experience across the department. Key...

About the Role The Research Governance Coordinator is a predominantly in‐office role located within the Windsor Research Unit at Fulbourn Hospital. The position requires 30 hours per week, spread over 4‐5 days (Monday‐Friday). The Coordinator leads a portfolio of studies across a range of specialties, providing consistent and competent expertise to researchers, clinicians and the research...

You will support audit readiness by ensuring files are reviewed on schedule detailed in the organization's WPD and department guidance document. If you are pursuing a career as a Clinical Research Associate (CRA), consider taking the first step with Thermo Fisher Scientific by applying for the position of Clinical Trial Coordinator.

We are supporting a growing clinical research site network seeking a Clinical Research Coordinator to support the day-to-day delivery of clinical trials at our Peterborough site. This is a hands-on, on-site role working closely with investigators, patients, and sponsors to ensure studies are run to GCP and protocol. Key Responsibilities Coordinate and support clinical trials from start-up to...

You will manage a complex caseload and deliver expert physiotherapy interventions, applying advanced clinical judgement and initiative to guide rehabilitation decisions. The complexity of care within our regional Major Trauma Centre provides a stimulating setting with scope for innovation and service development.

You must have appropriate UK professional registration.

Medicines Management Specialist - Neurodiversity Team Location: Remote Contract: Permanent | Full-time Are you an experienced Pharmacist and Independant Prescriber looking to take the next step in your career? Our client, a large Mental Health Provider, is looking for a Medicines Management Specialist to join their Neurodiversity team. What You’ll Do: - Provide clinical input on side effects...

Lead Electrical Protection Engineer 6 month contract initially Inside IR35 – Remote working 40 hours per week Job Summary: The preferred candidate is responsible for design preparation based on customer specification, conduct engineering activities from design stage until site commissioning and acts as a technical interface between customer and technical community. In-depth hands-on...

Contract – 8 Months Inside IR35 Remote – UK Power Systems Consultant (EMT & RMS Studies) The consultant will support power system projects across multiple phases by delivering high-quality electrical studies and technical documentation. Key Responsibilities - Develop and validate EMT and RMS models for assets such as WTGs, PPCs, and STATCOMs. - Plan and execute design and Grid Code...

INTERNATIONAL RECRUITMENT & HR EXPERTS ACROSS THE PLASTICS, PACKAGING, SPECIALITY CHEMICALS, LIFE SCIENCES, BIOPOLYMER, FOOD ADDITIVES & INGREDIENTS, ENERGY AND RECYCLING SECTORS SINCE 1975. Key Account Manager, Industrial & Electrical Polymer raw materials (Polyamides) Location: United Kingdom Job ref: CST/64702 Salary: Highly attractive – commensurate with experience The Company: Our...

GVP QA Auditing Manager Our client, a global Biopharma company, now have approval to hire a GVP QA Auditing Manager working as part of the Clinical Quality Assurance group within Global Quality Assurance in an entrepreneurial and fast-paced environment. This position has flexibility for remote work in Ireland or the UK. Some travel maybe required. The successful candidate will ensure the PV...

You will oversee a range of administrative, coordination and scientific tasks related to client projects, as well as contribute to company and team initiatives - Salary: £35,000 per annum

You will primarily work on Publications or Medical Affairs projects in this role. Key responsibilities will include:

You will manage a complex caseload and deliver expert physiotherapy interventions, applying advanced clinical judgement and initiative to guide rehabilitation decisions. The complexity of care within our regional Major Trauma Centre provides a stimulating setting with scope for innovation and service development.

Medicines Management Specialist - Neurodiversity Team Location: Remote Contract: Permanent | Full-time Are you an experienced Pharmacist and Independant Prescriber looking to take the next step in your career? Our client, a large Mental Health Provider, is looking for a Medicines Management Specialist to join their Neurodiversity team. What You’ll Do: - Provide clinical input on side effects...

You will work closely with the Senior Team Leader, CCIO and the Design Authority, requiring in‐depth technical knowledge of both the Epic application and the business and clinical processes across the organization.

You will work on a range of projects involving the set-up and management of de novo, global real-world evidence (RWE) studies, including ethics applications and site support

You will act as the primary contact for study management tasks, providing strategic leadership and ensuring high-quality delivery in line with ethical and regulatory standards.