CRA II - South West

PharmiWeb.jobs: Global Life Science Jobs; Maidenhead; On-site; GBP 60,000 - 80,000; Full time

Job summary

An innovative global organization is seeking Clinical Research Associates (CRAs II) to join their dynamic team in clinical research. This exciting role offers the opportunity to work on diverse studies while ensuring compliance with regulatory guidelines and company SOPs. You will conduct site monitoring visits, manage site activities, and mentor junior team members, all while contributing to groundbreaking advancements in clinical research. If you are ready to take the next step in your CRA career and thrive in a collaborative environment that values mentorship and growth, this opportunity is perfect for you.

Qualifications

• 2+ years of experience in clinical research or related roles.
• Basic knowledge of regulatory guidelines and clinical trial processes.

Responsibilities

• Conduct site monitoring visits to ensure compliance with protocols.
• Manage site activities including initiation, monitoring, and closeouts.

Skills

communication skills

organizational skills

problem-solving skills

Education

University/college degree in life sciences

Tools

GCP guidelines

Job description

Are you looking to grow your career in clinical research?
Fortrea is hiring CRAs II to join our dynamic team. We have opportunities based in South West, offering an exciting chance 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:

• University/college degree in life sciences or a relevant allied health field.
• At least 2 years of experience in a related role (e.g., Site Management, CRA).
• Basic knowledge of Regulatory Guidelines and the clinical trial process.
• Strong communication, organizational, and problem-solving skills.
• A valid driver’s license and willingness to travel.

Ready to take the next step in your CRA career? Apply now and be part of groundbreaking clinical research at Fortrea!