Clinical Research Associate II – Clinical Trial Services (Remote, United Kingdom)
Location: Remote – United Kingdom
Job Type: Full-time
Division: Precision for Medicine
Business Unit: Clinical Solutions
Requisition Number: 6319
About Precision for Medicine
Precision for Medicine is a leading, innovative contract research organization (CRO) specializing in precision oncology and rare diseases. Our team combines advanced biomarker analytics, adaptive trial designs, and deep scientific expertise to deliver actionable insights that optimize drug development pathways. With a culture centered on collaboration, growth, and work-life balance, Precision for Medicine consistently achieves high CRA retention rates and empowers employees to make meaningful contributions.
Role Overview
We are seeking a Clinical Research Associate II (CRA II) to join our Clinical Trial Services team. This fully remote UK-based role will provide oversight and monitoring of clinical trials, ensuring compliance with protocols, SOPs, ICH-GCP guidelines, and all applicable regulations. The CRA II will actively support study start-up, site initiation, monitoring, and close-out activities, serving as a key point of contact for investigative sites.
This position offers exposure to precision oncology trials, advanced clinical operations, and opportunities to develop into a protocol expert within a supportive, smaller CRO environment.
Key Responsibilities
Monitor and manage clinical study progress at investigative sites, ensuring trials are conducted in compliance with GCP, protocol, and regulatory requirements.
Coordinate study start-up activities, including site identification, regulatory submission support, pre-study visits, and initiation visits.
Identify potential study risks and proactively propose mitigation strategies.
Maintain high-quality study documentation, including source data verification, query resolution, and accurate reporting.
Act as a liaison between sites, sponsors, and cross-functional teams to ensure timely issue resolution.
Support early-phase and oncology-focused clinical trials as needed.
Contribute to continuous process improvements and knowledge sharing within the CRA team.
Required Qualifications
Bachelor’s degree or equivalent in life sciences or related field.
Minimum 1+ year of CRA experience within a CRO or pharmaceutical environment.
Proven ability to monitor and manage multiple clinical trial sites effectively.
Strong attention to detail with a proactive, problem-solving mindset.
Excellent communication skills in English.
Availability for domestic travel, including overnight stays (50–60% travel commitment); international travel may be required for senior-level roles.
Preferred Experience:
Oncology or early-phase clinical trial experience.
Familiarity with adaptive and targeted clinical trial designs.
Why Join Precision for Medicine?
Engage in cutting-edge oncology and rare disease research through precision medicine.
Work in a collaborative environment where your ideas and input are valued and can influence decision-making.
Maintain work-life balance with reasonable protocol loads and supportive management.
Access a culture that encourages professional growth, mentorship, and career development.
Precision for Medicine empowers employees to leverage biomarkers, advanced analytics, and scientific expertise to optimize clinical trial outcomes. Join a team that is transforming cancer treatment and advancing precision medicine globally.
Application Notes
Candidates should be cautious of fraudulent recruitment attempts. All formal offers from Precision for Medicine will be communicated directly through the official recruitment team following a structured interview process.
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Japan | Saitama |Tokyo :
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