Clinical Research Associate II – Senior Clinical Research Associate

🔥 15 minutes ago

🇬🇧 United Kingdom – Remote

⏰ Full Time

🟠 Senior

🧪 Clinical Research

👻 Ghost score 21%

What it means: the chance that no one is really hiring for this job.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

Apply Now

Find Similar Remote Jobs

Precision Medicine Group

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

Founded 2012

💼 Consulting

🏥 Healthcare

📦 Logistics

💰 $35.2M Venture Round on 2021-03

Consulting • Healthcare • Logistics

Precision Medicine Group is a global team of experts that specializes in precision medicine, which combines advanced lab sciences, translational informatics, regulatory affairs, payer insights, and marketing communications. The company focuses on overcoming product development and commercialization challenges for pharmaceutical and life sciences clients. Their services include biomarker-driven research and development, as well as commercialization support for life science organizations from launch to product maturity. Precision Medicine Group operates through two main arms: Precision for Medicine and Precision AQ, specializing in clinical and commercial solutions respectively.

📋 Description

• Monitor and own the progress of clinical studies at investigative sites • Ensure clinical studies are conducted, recorded, and reported according to protocol, SOPs, ICH-GCP, and applicable regulations and standards • Coordinate activities required to set up and monitor studies • Identify investigators • Help prepare regulatory submissions • Conduct pre-study and initiation visits • Attend investigator meetings, site visits, and project team updates • Identify study risks and propose mitigation solutions • Handle conflicts using resolution strategies • Support the execution of targeted, adaptive clinical trials in oncology and rare diseases

🎯 Requirements

• 4-year college degree or equivalent experience • More than 1 year of CRA experience within the CRO or pharmaceutical industry (ideally) • Oncology experience essential • Phase I experience desirable, although not essential • First-In-Human (FIH) experience desirable, although not essential • Availability for domestic travel, including overnight stays, of approximately 50–60% • Fluency in English • Must be legally authorized to work in the country of employment without employer sponsorship

🏖️ Benefits

• Extremely high CRA retention rates and supportive culture • Lower than average number of protocols • Reasonable travel and improved work/life balance • Direct line management support • Opportunity for influence and impact in a smaller CRO • Growth support • Fully home-based working

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Upload Resume