137 Clinical Research jobs in the United Kingdom

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.

Are you looking for an opportunity in Clinical Research? Do you want to work for an industry leading company. If so, come and join us - IQVIA are looking for a Clinical Research Coordinator.

This part-time role is to support a site in Halifax, West Yorkshire in conducting a clinical trial for 15 hours per week.

As a pivotal member of the site team, you will be involved with a variety of administrative tasks to support investigators and ensure the smooth running of clinical trials and assist with collecting patient data.

Day to day responsibilities will include:

• Support clinical research studies and maintain a safe study environment according to health and safety policies under the direction and delegation of the Principal Investigator
• Safeguard the well-being of subjects, act as a volunteer advocate, and address subject’s concerns
• Maintain up-to-date study protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems, and other study documents
• Plan and coordinate logistical activity for study procedures according to the study protocol
• Perform clinical set-up and preparation for the study including labeling specimen collection tubes and containers, inventory of required supplies, and setting up or troubleshooting equipment and/or study issues
• Assist with data entry, data quality checking, and query resolution to ensure adherence to study protocol and quality control for content accuracy and completeness
• Assist in study enrollment by recruiting, screening, and orienting volunteers according to the study protocol
• Correct custody of study drug according to site standard operating procedures
• Coordinate with study monitor on study issues and effectively respond to monitor-initiated questions.

We are looking for candidates with the following skills and experience:

• BS/BA in life sciences or educational equivalent and/or relevant work experience in a clinical environment or medical setting, e.g. clinical research coordinator, nurse, medical assistant, other medical profession
• Basic knowledge of clinical trials, combined with in-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and study schedules
• Basic knowledge of medical terminology
• Strong IT competence, skilled in using MS Windows and Office applications such as Access, Outlook, Excel, and Word
• Excellent interpersonal skills with the ability to establish and maintain effective working relationships with co-workers, managers and client
• Good organizational skills with the ability to pay close attention to detail.

Are you looking for an opportunity in Clinical Research? Do you want to work for an industry leading company. If so, come and join us - IQVIA are looking for a Clinical Research Coordinator.

This part-time role is to support a site in Oldham in conducting a clinical trial for 16 hours per week.

As a pivotal member of the site team, you will be involved with a variety of administrative tasks to support investigators and ensure the smooth running of clinical trials and assist with collecting patient data.

Day to day responsibilities will include:

• Support clinical research studies and maintain a safe study environment according to health and safety policies under the direction and delegation of the Principal Investigator
• Safeguard the well-being of subjects, act as a volunteer advocate, and address subject’s concerns
• Maintain up-to-date study protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems, and other study documents
• Plan and coordinate logistical activity for study procedures according to the study protocol
• Perform clinical set-up and preparation for the study including labeling specimen collection tubes and containers, inventory of required supplies, and setting up or troubleshooting equipment and/or study issues
• Assist with data entry, data quality checking, and query resolution to ensure adherence to study protocol and quality control for content accuracy and completeness
• Assist in study enrollment by recruiting, screening, and orienting volunteers according to the study protocol
• Correct custody of study drug according to site standard operating procedures
• Coordinate with study monitor on study issues and effectively respond to monitor-initiated questions.

We are looking for candidates with the following skills and experience:

• BS/BA in life sciences or educational equivalent and/or relevant work experience in a clinical environment or medical setting, e.g. clinical research coordinator, nurse, medical assistant, other medical profession
• Basic knowledge of clinical trials, combined with in-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and study schedules
• Basic knowledge of medical terminology
• Strong IT competence, skilled in using MS Windows and Office applications such as Access, Outlook, Excel, and Word
• Excellent interpersonal skills with the ability to establish and maintain effective working relationships with co-workers, managers and client
• Good organizational skills with the ability to pay close attention to detail.

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:

Our client, an innovative clinical research organisation (CRO) is currently looking for a Clinical Research Physician to join their team in London.

As a Clinical Research Physician, you will spearhead early stage clinical trials, manage study protocols and ensure ethical conduct and compliance at all stages. You will collaborate with an expert sponsor team and contribute to ground-breaking projects that advance healthcare and improve patient outcomes.

You will be driven to enhance patient safety, improve quality systems and ensure the data produced for the development of individual drugs is of the highest standard.

This role will offer tremendous scope for leadership and personal development. With this site being relatively new, this person will have the remit to grow and nurture a clinical research team around them as well as having significant involvement and influence with their sponsors.

Key Responsibilities

• Provide medical direction, oversee protocol compliance and ensure participant safety throughout clinical trials.
• Evaluate and interpret clinical data, performing necessary assessments to maintain data accuracy and integrity.
• Collaborate on scientific feasibility for new inquiries, assisting sponsors and guiding clinical operations teams as needed.
• Ensure adherence to regulatory requirements and Good Clinical Practice standards, maintaining rigorous documentation and participant confidentiality.

Requirements

• A medical degree (MD) - essential
• Full and current GMC registration - essential.
• Strong background in clinical research / clinical trials.
• Proven experience as a Clinical Research Physician.
• Strong knowledge of regulatory guidelines.
• Excellent organisational, communication and analytical skills.

Park Street People Ltd is an Equal Opportunities Employer. We do not discriminate on the grounds of age, race, gender, disability, creed or sexual orientation and comply with all relevant UK legislation. We are acting as an Employment Agency in relation to this role.

Our client, an innovative clinical research organisation (CRO) is currently looking for a Clinical Research Physician to join their team in London.

As a Clinical Research Physician, you will spearhead early stage clinical trials, manage study protocols and ensure ethical conduct and compliance at all stages. You will collaborate with an expert sponsor team and contribute to ground-breaking projects that advance healthcare and improve patient outcomes.

You will be driven to enhance patient safety, improve quality systems and ensure the data produced for the development of individual drugs is of the highest standard.

This role will offer tremendous scope for leadership and personal development. With this site being relatively new, this person will have the remit to grow and nurture a clinical research team around them as well as having significant involvement and influence with their sponsors.

Key Responsibilities

• Provide medical direction, oversee protocol compliance and ensure participant safety throughout clinical trials.
• Evaluate and interpret clinical data, performing necessary assessments to maintain data accuracy and integrity.
• Collaborate on scientific feasibility for new inquiries, assisting sponsors and guiding clinical operations teams as needed.
• Ensure adherence to regulatory requirements and Good Clinical Practice standards, maintaining rigorous documentation and participant confidentiality.

Requirements

• A medical degree (MD) - essential
• Full and current GMC registration - essential.
• Strong background in clinical research / clinical trials.
• Proven experience as a Clinical Research Physician.
• Strong knowledge of regulatory guidelines.
• Excellent organisational, communication and analytical skills.

Park Street People Ltd is an Equal Opportunities Employer. We do not discriminate on the grounds of age, race, gender, disability, creed or sexual orientation and comply with all relevant UK legislation. We are acting as an Employment Agency in relation to this role.