CRA II / SCRA II Midlands

CRA II / SCRA II Midlands

Full-Time 40000 - 50000 Β£ / year (est.) No working from home possible
Meeveem Limited

At a Glance

  • Tasks: Conduct site monitoring visits and ensure compliance with protocols in clinical research.
  • Company: Join Fortrea, a global leader in innovative clinical research.
  • Benefits: Flexible career progression, mentorship, and a collaborative team environment.
  • Other info: Exciting opportunities for growth in a supportive and dynamic workplace.
  • Why this job: Make a real impact on diverse studies while advancing your career.
  • Qualifications: Degree in life sciences and 2 years of relevant experience required.

The predicted salary is between 40000 - 50000 Β£ per year.

  • Description
  • Are you looking to grow your career in clinical research? Fortrea is hiring a

CRA II/SCRA to join our dynamic FSP team. We have opportunities across the UK, particularly in 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

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.

Learn more about our EEO & Accommodations request.

At Fortrea, we're all about turning the "impossible" into "I'm possible." Together, we break barriers to deliver exceptional service to our patients, fueled by a shared commitment to teamwork and excellence.

Regardless of your role, we're all family, working together to achieve extraordinary results.

At Fortrea, your career isn't just a job – it's a journey of making the exceptional possible, every day.

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CRA II / SCRA II Midlands employer: Meeveem Limited

Meeveem Limited is an exceptional employer that values its employees by fostering a collaborative and innovative work culture in the heart of Yorkshire. With a strong focus on professional development, employees are encouraged to grow their skills and advance their careers while enjoying competitive benefits and a supportive environment that prioritises work-life balance. Joining Meeveem means being part of a dynamic team dedicated to making a meaningful impact in the cardiovascular and endovascular sectors.

Meeveem Limited

Contact Details:

Meeveem Limited Recruitment Team

We think you need these skills to ace CRA II / SCRA II Midlands

Clinical Research
Site Monitoring
Regulatory Compliance
Good Clinical Practice (GCP)
Feasibility Assessments
Investigator Recruitment
Vendor Coordination