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CRA II/Senior CRA

Precision Medicine Group

United Kingdom

Remote

GBP 60,000 - 80,000

Full time

7 days ago
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Job summary

An innovative and passionate company in the CRO sector is seeking a CRA II/Senior CRA to join their fully remote team in the UK. This role offers a unique opportunity to manage clinical studies with a focus on quality and detail, ensuring compliance with protocols and regulations. Enjoy a supportive work environment where your contributions are valued, and you can influence significant projects in the field of precision medicine. With a commitment to work-life balance and reasonable travel expectations, this position is perfect for those looking to make a meaningful impact in oncology research.

Qualifications

  • At least 2 years of CRA experience in CRO or pharmaceutical industry.
  • Fluency in English, with oncology experience preferred.

Responsibilities

  • Monitor and own the progress of clinical studies at investigative sites.
  • Coordinate activities required to set up and monitor a study.

Skills

Detail-oriented
Conflict resolution
Problem-solving
Project management
Communication

Education

4-year college degree
Graduate or postgraduate degree in scientific or healthcare discipline

Job description

Precision for Medicine is not your typical CRO. We are passionate about cultivating our culture and are proud to share extremely high CRA retention rates compared to industry averages.

CRAs join us, love their jobs, and stay because of the amazing people and enjoyable quality of life. You will have a lower than average number of protocols, setting you up to be a protocol expert. Travel is reasonable and your work/life balance will benefit as a result. Most meaningfully - your voice will be heard. Working in a smaller CRO allows you to have influence and impact when it matters most and support from direct line management.

We are hiring a CRA II/Senior CRA, this position will be fully home based working in the UK.

About you:
  • You are calm, thoughtful, and responsive when things don’t go as planned.
  • You are well-prepared, whether it be for an investigator meeting, site visit or project team update, always staying two steps ahead of the game.
  • You find quick and creative ways of overcoming difficulties.
  • You have an impeccable eye for detail.
  • You identify potential study risks and propose solutions on how to mitigate them.
  • You take responsibility in the quality and outcomes of your work.
  • You are adept at handling conflict by using tried and true resolution strategies.
How we will keep you busy and support your growth:

You will monitor and own the progress of clinical studies at investigative sites and ensure that clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations and standards. You will coordinate all necessary activities required to set up and monitor a study (i.e., identify investigators; helping prepare regulatory submissions, conducting pre-study and initiation visits, etc.).

Qualifications:
  • 4-year college degree or equivalent experience
Other Required:
  • Candidates should ideally have at least 2 years CRA experience within the CRO or pharmaceutical industry.
  • Oncology experience, early phase experience desirable although not essential.
  • Availability for domestic travel including overnight stays, which may constitute up to approximately 50-60% travel commitment (international travel may be required for some senior level positions)
  • Fluency in English
Preferred:
  • Graduate or postgraduate degree with a concentration in a scientific or healthcare discipline

Precision’s uniquely integrated offering enables the science of precision medicine by combining novel clinical trial designs, industry-leading operational and medical experts, advanced biomarker and data analytics solutions, and an unequivocal real passion for rare diseases and oncology.

Precision medicine is revolutionizing the attack on cancer—and we are passionate about helping you harness its power. We strike tumors on a molecular level using biomarkers to link specific mutations to specific treatments. We combine deep science with deep data from advanced technological platforms, then layer on specialized expertise in the design and execution of targeted, adaptive clinical trials. Ultimately, we deliver robust insights that inform real-time decisions—and optimize the oncology development pathway.

We invite you to learn more about our growing organization serving our clients that are researching groundbreaking cancer therapies. We strive to ensure employees feel appreciated for the contributions they make every single day. You will provide input and have your ideas valued and nurtured, impacting positive change for the company.

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