Senior Clinical Research Associate

🔥 1 minute ago

🇵🇱 Poland – Remote

⏰ Full Time

🟠 Senior

🧪 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, 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 with 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 with a concentration 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 • Support from direct line management • Opportunity to train and mentor junior staff members • Input and ideas valued and nurtured • Equal opportunity employment • Reasonable accommodation available for applicants with disabilities