Clinical Research Associate II

🕒 5 days ago

🇪🇸 Spain – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

🧪 Clinical Research

👻 Ghost score 10%

What it means: how likely this posting is sitting open without active hiring.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.

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Precision For Medicine

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

🏥 Healthcare

💼 Consulting

📦 Logistics

💰 $75M Private Equity Round on 2015-12

Healthcare • Consulting • Logistics

Precision For Medicine is a leading organization that specializes in supporting the development and commercialization of innovative therapies, particularly in oncology, rare diseases, and autoimmune conditions. With a comprehensive range of services including clinical trial management, lab services, and biospecimen collection, they integrate advanced biomarker capabilities and manufacturing solutions to streamline the complex clinical development processes. Their mission is to accelerate research and bring life-changing medical solutions to patients by overcoming traditional inefficiencies typically found in the pharmaceutical development landscape.

📋 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 all 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 • Participate in investigator meetings, site visits, and project team updates • Identify potential study risks and propose mitigation solutions • Manage conflict using resolution strategies • Provide input and ideas to support positive company change

🎯 Requirements

• 4-year college degree or equivalent experience • 2 (two) years or more as a CRA in either a CRO or pharmaceutical/ biotech industry or equivalent, relevant experience and/or demonstrated competencies • Site management or equivalent experience in clinical research • Oncology monitoring experience • Availability for domestic travel including overnight stays, up to approximately 50–60% travel commitment • Fluency in English and, for non-English speaking countries, the local language of the country where the position is based • Candidates must reside in Madrid or Barcelona • Application must be submitted in English • Graduate or postgraduate degree with a concentration in a scientific or healthcare discipline preferred • Phase I experience preferred • Experience managing CAR-T/FIH studies preferred

🏖️ Benefits

• Extremely high CRA retention rates compared to industry averages • Lower than average number of protocols • Reasonable travel commitment • Improved work/life balance • Direct line management support • Opportunities to influence and impact company decisions • Employee input and ideas valued and nurtured