Clinical Research Associate II/Senior Clinical Research Associate

Precision for Medicine; United Kingdom; Remote; GBP 40,000 - 60,000; Full time

Job summary

A leading clinical research organization in the UK is seeking a Clinical Research Associate II/Senior Clinical Research Associate for a fully remote position. The ideal candidate will have a minimum of 2 years of CRA experience, with a focus on oncology preferred but not essential. Responsibilities include monitoring clinical studies and ensuring adherence to regulatory standards. This role offers a balanced work/life environment and opportunities for professional growth.

Qualifications

• Minimum 2 years CRA experience within the CRO or pharmaceutical industry.
• Availability for domestic travel including overnight stays.
• Early phase experience is desirable but not essential.

Responsibilities

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

Skills

CRA experience

Oncology experience

Fluency in English

Education

4-year college degree or equivalent experience

Job description

Overview

Clinical Research Associate II/Senior Clinical Research Associate – Remote, United Kingdom. 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.

Responsibilities

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, including:

• Identify investigators
• Help prepare regulatory submissions
• Conduct pre-study and initiation visits

Qualifications

• 4-year college degree or equivalent experience
• Candidates should have at least 2 years CRA experience within the CRO or pharmaceutical industry
• Oncology experience and/or early phase experience desirable but not essential
• Availability for domestic travel including overnight stays, up to approximately 50–60% travel commitment (international travel may be required for some senior level positions)
• Fluency in English

Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law.