CRA II North West

Fortrea; Maidenhead; On-site; GBP 30,000 - 45,000; Full time

Job summary

A global clinical research organization is seeking a CRAII to join their team in the North West of England. This role offers an exciting opportunity to work on diverse clinical studies while ensuring compliance with regulatory guidelines. The ideal candidate will have a degree in Life Sciences, three years of relevant clinical research experience, including monitoring, and possess strong communication skills. The position requires regular travel, and the organization values career growth within the field.

Benefits

Flexible career progression

Collaborative team environment

Mentorship opportunities

Qualifications

• 3 years of relevant clinical research experience with at least 1 year of previous monitoring experience.
• Ability to work independently and manage multiple priorities.
• Strong communication, organizational and problem‑solving skills.

Responsibilities

• Conduct and oversee study site monitoring visits to ensure compliance.
• Manage all aspects of site activities including site initiation monitoring visits.
• Ensure patient safety data integrity and adherence to GCP guidelines.

Skills

Business Development

Customer Service

Project Management

Ensure Compliance

Education

Bachelors or Masters degree in Life Sciences or equivalent

Job description

Are you looking to grow your career in clinical research

Fortrea is hiring a CRAII to join our client-dedicated team. This role is based in the North West offering an exciting opportunity to work on diverse studies while ensuring compliance with regulatory guidelines and company SOPs.

Why Join Fortrea

• Be part of a global innovative organization driving advancements in clinical research.
• Work on cutting‑edge trials across a range of therapeutic areas.
• Enjoy flexible career progression with opportunities at different CRA levels.
• Benefit from a collaborative team environment that values mentorship and growth.

Key Responsibilities

• Conduct and oversee study site monitoring visits to ensure compliance with protocols and regulatory requirements.
• Manage all aspects of site activities including site initiation monitoring visits and closeouts.
• Ensure patient safety data integrity and adherence to GCP guidelines.
• Support feasibility assessments, investigator recruitment and vendor coordination.
• Mentor junior team members and contribute to quality control efforts.
• Track and report Serious Adverse Events (SAEs) as required.

Qualifications

• Bachelors or Masters degree in Life Sciences or equivalent.
• 3 years of relevant clinical research experience with at least 1 year of previous monitoring experience.
• Ability to work independently and manage multiple priorities.
• Basic knowledge of regulatory guidelines and the clinical trial process.
• Strong communication, organizational and problem‑solving skills.
• Valid drivers license and willingness to travel nationally (68 visits / month).

Ready to take the next step in your CRA career

Apply now and be part of groundbreaking clinical research at Fortrea!

Learn more about our EEO & Accommodations request here .

Key Skills

• Business Development
• Company Policies
• Customer Service
• Financial Performance
• Revenue Growth
• Oversight
• Regional Sales
• Account Management
• Project Management
• Product Line
• Ensure Compliance
• Human Resources
• Procedures
• Sales Goals
• Direct Reports

Employment Type : Full-Time

Experience : years

Vacancy : 1