Senior Clinical Research Associate

Precision AQ; United Kingdom; Remote; GBP 54,000 - 76,000; Full time

Job summary

Precision for Medicine is seeking a Senior Clinical Research Associate who will work fully from home in the UK or Northern Ireland. The role requires monitoring clinical studies at investigative sites and ensuring compliance with protocol, SOPs, ICH-GCP, and regulations.

Ideal candidates have a 4-year degree and 3+ years of CRA experience within CRO/pharma; some travel may be required. Fluency in English is essential, with Phase I and FIH experience a plus.

Qualifications

• 4-year college degree or equivalent experience.
• Candidates should ideally have more than 3.5 years CRA experience within the CRO or pharmaceutical industry.
• Phase I experience desirable but not essential.
• First-In-Human (FIH) desirable but not essential.
• Availability for domestic travel up to 50-60% (international travel may be required for some senior positions).
• Fluency in English.

Responsibilities

• Monitor and own the progress of clinical studies at investigative sites.
• Ensure studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and applicable regulations.
• Coordinate activities to set up and monitor a study, identify investigators, assist with regulatory submissions, pre-study and initiation visits.

Skills

Fluency in English

Education

4-year college degree or equivalent experience

Job description

Location: Remote, United Kingdom
Category: Clinical Trial Services
Division: Precision for Medicine
Business Unit: Clinical Solutions
Requisition Number: 7330

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 Senior Clinical Research Associate, this position will be fully home based working in the UK or Northern Ireland.

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 more than 3,5 years CRA experience within the CRO or pharmaceutical industry.
• Phase I experience desirable although not essential
• First-In-Human (FIH) 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

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.

Candidates must be legally authorized to work in the country of employment without employer sponsorship.

If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process, or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at [e-mail] .