CRA II Midlands

PharmiWeb.jobs: Global Life Science Jobs; Maidenhead; On-site; GBP 30,000 - 50,000; Full time

Job summary

Fortrea is seeking CRAs at various seniority levels to join their dynamic team in London and the Midlands. As part of a global organization, you will conduct site monitoring visits, manage site activities, and support compliance with regulatory requirements. The role offers career progression and a collaborative environment focused on mentorship. Candidates should possess a relevant degree, experience in clinical research, and strong communication skills.

Benefits

Flexible career progression

Collaborative team environment

Qualifications

• 1+ year of experience in a related role (e.g., Site Management, CRA).
• Basic knowledge of Regulatory Guidelines and clinical trial process.
• Valid driver's license and willingness to travel.

Responsibilities

• Conduct and oversee study site monitoring visits to ensure compliance.
• Manage all aspects of site activities, including initiation and monitoring.
• Mentor junior team members and contribute to quality control efforts.

Skills

Communication

Organizational

Problem-Solving

Education

University/college degree in life sciences

Job description

Are you looking to grow your career in clinical research? Fortrea is hiring CRAs at various seniority levels to join our dynamic team. We have opportunities based in London and the Midlands, 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 1 year 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!

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