Precision Medicine Group
Clinical Research Associate II
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Clinical Research Associate II
Clinical Research Associate II – Home-Based (UK/Northern Ireland)
Precision for Medicine is not your typical CRO. We are passionate about cultivating a supportive culture with extremely high CRA retention rates compared to industry standards.
Why Join Us? CRAs thrive here for:
- Lower protocol load, helping you build deep protocol expertise
- Reasonable travel (domestic, ≤50-60% commitment; international only required for rare senior roles)
- Superior work-life balance, aligning with our business model
- Meaningful influence—smaller team size means active participation in critical decisions
- Exclusive focus on precision medicine, rare disease, and oncology
- Collaborative culture with strong direct line-manager support
The Role: Clinical Research Associate II
Location: Home-based in the UK or Northern Ireland Purpose: You will own and advance clinical trial progress by ensuring flawless conduct, documentation, and reporting of studies across multiple investigative sites. Key tasks include:
- Monitoring adherence to protocol, SOPs, ICH-GCP, and regulatory standards
- Overseeing all study setup activities (e.g., investigator identification, regulatory submissions, pre-study visits)
- Conducting high-quality, impactful site visits
Your Impact: About You
We seek a naturally proactive, detail-oriented professional who:
- Remains calm and solution-oriented during unforeseen challenges
- Proactively manages risks, anticipating and mitigating potential issues
- Resolves conflict with measured, solutions-driven approaches
- Leverages creativity to overcome hurdles the moment they arise
- Delivers outstanding quality work, taking personal ownership
- Prepares meticulously—anticipating preparatory tasks for meetings, visits, or project updates
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How We’ll Support Your Growth
Core Responsibilities
- Act as the study voice at investigator sites, ensuring protocol compliance and high-integrity data collection
- Collaborate with investigators, biostatistics teams, and medical safety assessors to optimise trial execution
- Provide substantive input at protocols’, medical, and regulatory review meetings
- Assess study risk-management strategies across all study phases, from design to conclusion
Your Qualifications: Minimum (Non-Negotiable)
✅ 4-year college degree (or equivalent work experience navigating clinical trial contexts) ✅ GCP certification recommended (BATNA 10+ hours) to support your expertise
Mandatory Industry Experience (Essential to baseline competence.)
✅ Demonstratable CRA experience of >1 year either in a CRO or pharma setting ✅ Up-to-date understanding of ICH-GCP, COGA (File Cloning), and FDA/NICE standards
Highly Valued Competences (Challenges characteristic of Oncology/Rare Diseases will likely arise; role-accelerating advantage to have.)
✅ Oncology or early-phase trial experience (preferred but not mandatory) ✅ Advanced responsibilities within a world-class CRO, peer networks, and oncology client environments
What They’re Saying About Precision Medicine
“Precision Medicine Group’s uniquely integrated offering transforms oncology—we revolutionise by combining: + Cutting-edge trial design + Agile biomarker solutions + Advanced data analytics + Rare-disease focus through single company expertise Our work enables personalised, molecular attack on tumours, driving scientific innovation and real-time decision-making in drug development.”
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Why Princess Crossroad May Be the Right Move for You:
Benefits and Culture
- Robust consultations—clinical expertise often translates to peer recognition, with integral input at company’s growth milestones
- Ownership of projects: unlike large CROs, priorities are collaborative, empowering you to directly drive outcomes
- Unprecedented freedom within accountability: Managing your time to balance UK/IE work-life expectations in a "smaller player" system
Delivery of Purpose
*“By pioneering precision therapy from biomarker through patient benefit, we ensure long term genuine value in our clients’ pipelines. Join us to foster change.”
DUAL BECAUSE? (Our Commitment to Valuing You)
Precision Medicine Group prohibits any unacceptable bias. Instead, we prioritise a philosophy grounded in fair, transparent hiring practices:
- Equal opportunity regardless of race, age, religion, sexual orientation, disability (including diversity in experience upon hiring).
- Providing reasonable accommodation to qualified applicants adhering to accessibility requirements. Request your reasonable accommodations, inclusive of alternative application processes, to myHR@precisionmedicinegrp.com as early as possible.
- Transparent application commitments: No fraudulent scams or unjust requests (e.g., no recruitment-stage demands for bank details or pre-paid employment ‘fees’).
Contact Us Directly
Outer Shepherd Care Workforce includes our focal point, myHR@precisionmedicinegrp.com, should you need to discuss requests for adjusted formats necessary for effective application or accessibility.
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