Senior Clinical Research Associate

🔥 0 minutes ago

🇵🇱 Poland – Remote

⏰ Full Time

🟠 Senior

🧪 Clinical Research

👻 Ghost score 20%

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 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, 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 • Handle appropriately sized clinical trials • Support Project Managers on larger-scope trials • Train and mentor junior staff members • Interact directly with clients • Initiate payments • Participate in proposal activities, including development and client presentations

🎯 Requirements

• 4-year college degree or equivalent experience • 3+ years of independent monitoring experience within the CRO or pharmaceutical industry • Experience managing oncology studies • Availability for domestic travel including overnight stays, approximately 50–60% travel commitment • International travel may be required for some senior-level positions • Fluency in Polish and English • Candidates must be legally authorized to work in the country of employment without employer sponsorship • Preferred: graduate or postgraduate degree in a scientific or healthcare discipline • Preferred: experience managing CAR-T/phase I studies • Preferred: study start-up activities experience • Preferred: understanding of financial management

🏖️ Benefits

• Fully home-based work option • Reasonable travel and improved work/life balance • Direct line management support • Opportunity to train and mentor junior staff members • Employee input and ideas valued and nurtured • Equal opportunity employment • Reasonable accommodation support during the application process