1,266 Clinical Positions jobs in the United Kingdom

Job Title: Clinical Research Coordinator (Band 6 Nurse)

Contract Type: Part-Time (2–3 days/week)

Overview:

We are seeking a skilled and motivated Band 6 Nurse to support clinical research activities as a Clinical Research Coordinator. This part-time role offers an excellent opportunity to contribute to impactful research while maintaining a flexible schedule.

Key Responsibilities:

• Identify and recruit eligible patients for clinical trials.
• Perform accurate and timely data entry into study databases.
• Collaborate with research and clinical teams to ensure protocol compliance.
• Maintain high standards of documentation and regulatory adherence.

Requirements:

• Registered Band 6 Nurse with relevant clinical experience.
• Demonstrated experience in patient identification and data entry.
• Strong attention to detail and organizational skills.
• Must be available to work every Wednesday, plus two additional weekdays.

Please submit your CV or get in touch via email:

Job Title: Junior Clinical Research Associate (CRA)

Location: London, UK (Field-based with regular site visits)

Employment Type: Full-time

About the Role:

We are seeking a motivated Junior Clinical Research Associate (CRA) with a minimum of 2 years of independent monitoring experience to join our London-based team. The successful candidate will play a vital role in ensuring the quality and integrity of clinical trials across multiple therapeutic areas. You will conduct 4–6 monitoring visits per month , providing oversight of study sites while maintaining compliance with ICH-GCP, local regulations, and study protocols.

Key Responsibilities:

• Perform routine monitoring visits (site initiation, interim, and close-out) across assigned sites in London and surrounding regions.
• Ensure adherence to protocol, ICH-GCP, and applicable regulatory requirements.
• Verify accuracy and completeness of case report forms (CRFs) against source data.
• Identify and resolve data discrepancies and protocol deviations in collaboration with site staff.
• Maintain effective communication with investigators, site personnel, and internal study teams.
• Prepare and submit timely monitoring reports and follow-up documentation.
• Support investigators and sites in resolving queries and ensuring readiness for audits and inspections.
• Contribute to trial start-up activities when required (e.g., site feasibility, essential document collection).

Requirements:

• Bachelor’s degree in Life Sciences, Nursing, Pharmacy, or related field.
• Minimum 2 years of independent monitoring experience within a CRO, pharmaceutical, or biotech environment.
• Strong knowledge of ICH-GCP and UK clinical trial regulations.
• Excellent organizational and time management skills with the ability to manage multiple sites.
• Willingness to travel frequently (4–6 site visits per month).
• Strong interpersonal and communication skills, both written and verbal.

What We Offer:

• Competitive salary and benefits package.
• Professional development opportunities within a growing clinical operations team.
• Exposure to diverse therapeutic areas and phases of clinical development.
• Supportive work environment with mentorship from senior CRAs.

Job Title: Junior Clinical Research Associate (CRA)

Location: London, UK (Field-based with regular site visits)

Employment Type: Full-time

About the Role:

We are seeking a motivated Junior Clinical Research Associate (CRA) with a minimum of 2 years of independent monitoring experience to join our London-based team. The successful candidate will play a vital role in ensuring the quality and integrity of clinical trials across multiple therapeutic areas. You will conduct 4–6 monitoring visits per month , providing oversight of study sites while maintaining compliance with ICH-GCP, local regulations, and study protocols.

Key Responsibilities:

• Perform routine monitoring visits (site initiation, interim, and close-out) across assigned sites in London and surrounding regions.
• Ensure adherence to protocol, ICH-GCP, and applicable regulatory requirements.
• Verify accuracy and completeness of case report forms (CRFs) against source data.
• Identify and resolve data discrepancies and protocol deviations in collaboration with site staff.
• Maintain effective communication with investigators, site personnel, and internal study teams.
• Prepare and submit timely monitoring reports and follow-up documentation.
• Support investigators and sites in resolving queries and ensuring readiness for audits and inspections.
• Contribute to trial start-up activities when required (e.g., site feasibility, essential document collection).

Requirements:

• Bachelor’s degree in Life Sciences, Nursing, Pharmacy, or related field.
• Minimum 2 years of independent monitoring experience within a CRO, pharmaceutical, or biotech environment.
• Strong knowledge of ICH-GCP and UK clinical trial regulations.
• Excellent organizational and time management skills with the ability to manage multiple sites.
• Willingness to travel frequently (4–6 site visits per month).
• Strong interpersonal and communication skills, both written and verbal.

What We Offer:

• Competitive salary and benefits package.
• Professional development opportunities within a growing clinical operations team.
• Exposure to diverse therapeutic areas and phases of clinical development.
• Supportive work environment with mentorship from senior CRAs.

Job Title: Freelance Clinical Research Associate – Associate Level (Oncology)

Location: Hybrid UK Based

Employment Type: Freelance

Function: Clinical Operations

Therapeutic Area: Oncology

Reports To: Clinical Operations Manager

About the Role

We are seeking a motivated and detail-oriented Freelance Clinical Research Associate (Associate Level) with a passion for oncology clinical trials. This is an exciting opportunity for an early-career CRA to gain hands-on experience in a dynamic, cross-functional research environment. You will support clinical trial activities across multiple oncology study sites, ensuring compliance with regulatory guidelines, ICH-GCP, and study protocols.

Key Responsibilities

• Conduct site monitoring visits (pre-study, initiation, routine, and close-out) for oncology clinical trials in accordance with study protocols and regulatory requirements.
• Assist in site selection and feasibility assessments.
• Ensure proper documentation and timely resolution of site issues.
• Support site staff in understanding and complying with study protocols and GCP guidelines.
• Verify source data and case report forms (CRFs) for accuracy, completeness, and consistency.
• Ensure timely collection and review of essential regulatory documents.
• Track patient recruitment and retention efforts at assigned sites.
• Participate in CRA training sessions, project team meetings, and sponsor meetings as required.
• Maintain high-quality communication with clinical sites and sponsor/CRO teams.
• Escalate site performance or compliance issues as needed.

Required Qualifications

• Bachelor’s degree or higher in Life Sciences, Nursing, Pharmacy, or a related field.
• Minimum of 1–2 years of clinical research experience (internships or study coordinator experience may be considered).
• Exposure to oncology trials (academic, site, or CRO experience).
• Understanding of ICH-GCP guidelines and regulatory requirements.
• Strong organizational skills with attention to detail.
• Ability to manage multiple tasks and priorities independently.
• Excellent communication and interpersonal skills.
• Proficiency with clinical trial management systems (CTMS), EDC systems, and Microsoft Office.

• Initiate, monitor, and close-out clinical trial sites according to study protocols and regulatory guidelines.
• Ensure the accurate and timely collection, verification, and reporting of clinical data.
• Conduct site visits (qualification, initiation, monitoring, and close-out) to assess patient safety, data integrity, and protocol compliance.
• Train and support site staff on study-specific procedures, data entry, and regulatory requirements.
• Resolve data discrepancies and outstanding issues with investigators and site staff.
• Prepare and present study progress reports to project teams and management.
• Maintain communication with investigators, site personnel, and study sponsors.
• Ensure all study-related documentation is maintained accurately and comprehensively.
• Participate in the development of study protocols and other trial-related documents.
• Adhere to company policies and procedures, as well as GCP and relevant regulatory standards.

• Bachelor's degree in a life science, nursing, or a related field.
• Previous experience as a Clinical Research Associate or in a similar clinical research role.
• Thorough understanding of GCP, ICH guidelines, and relevant regulatory requirements.
• Proficiency in using clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
• Excellent organizational, analytical, and problem-solving skills.
• Strong communication and interpersonal skills, with the ability to build rapport with site personnel.
• Ability to manage multiple priorities and work effectively under pressure.
• Willingness to travel to clinical trial sites as required.
• Proficiency in English, both written and spoken.

• Design, develop, and manage clinical trial protocols.
• Oversee the execution of clinical studies, ensuring compliance with GCP and regulatory guidelines.
• Analyze and interpret clinical trial data to assess drug safety and efficacy.
• Prepare comprehensive study reports, scientific publications, and regulatory submissions.
• Collaborate with internal teams (e.g., R&D, regulatory, medical affairs) and external stakeholders (e.g., investigators, CROs).
• Manage budgets and timelines for assigned clinical trials.
• Identify and evaluate potential clinical investigators and sites.
• Provide scientific and technical expertise throughout the drug development process.
• Stay abreast of scientific advancements and therapeutic area developments.
• Contribute to the strategic direction of clinical development programs.