Experienced CRAs

Fortrea; Remote; GBP 40,000 - 60,000; Full time

Job summary

A global innovative organization in clinical research is hiring experienced Clinical Research Associates (CRAs) to join their team. This remote role offers exciting opportunities to manage clinical trials while ensuring regulatory compliance. Ideal candidates will have 3 years of clinical research experience and 2 years of independent monitoring experience. This position allows for flexible career advancement in a collaborative team environment. Apply now to be part of groundbreaking clinical research!

Qualifications

• At least 2 years of previous monitoring experience.
• 3 years of relevant clinical research experience.
• Basic knowledge of regulatory guidelines and the clinical trial process.

Responsibilities

• Conduct and oversee study site monitoring visits.
• Manage all aspects of site activities.
• Ensure patient safety data integrity and adherence to GCP guidelines.
• Support feasibility assessments and vendor coordination.
• Mentor junior team members.

Skills

Independent monitoring experience

Strong communication skills

Organizational skills

Problem-solving skills

Education

Bachelors or Masters degree in Life Sciences

Job description

Are you looking to grow your career in clinical research

Fortrea is hiring experienced CRAs ( minimum of 2 years of independent monitoring experience ) on different levels of seniority to join our client-dedicated team. This role is remote 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 2 years 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 .

Required Experience :

Senior IC

Employment Type : Full-Time

Experience : years

Vacancy : 1