Clinical Research Associate

🕒 August 4

🇩🇪 Germany – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

🧪 Clinical Research

👻 Ghost score 18%

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 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 • Focus on an average of one to two studies and become a protocol expert • Identify potential study risks and propose mitigation solutions

🎯 Requirements

• Graduate or postgraduate degree with a concentration in a scientific or healthcare discipline • At least one year as a CRA in a CRO or pharmaceutical/biotech industry, or equivalent relevant experience and/or demonstrated competencies • Site management or equivalent experience in clinical research • Excellent communication and organizational skills • Team-player capability • Evidence of a client-focused approach • Availability for domestic travel, including overnight stays, up to approximately 50–60%; international travel may be required for some senior positions • Fluency in English and German • Experience in oncology, CAR-T, or FIH studies (phase III)

🏖️ Benefits

• Reasonable travel and improved work/life balance • Support from direct line management • Opportunity for influence and impact in a smaller CRO • Employee contributions and ideas valued and nurtured