Clinical Research Associate II

🔥 0 minutes ago

🇪🇸 Spain – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

🧪 Clinical Research

👻 Ghost score 21%

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, and applicable regulations and standards • Coordinate activities required to set up and monitor studies • Identify investigators • Help prepare regulatory submissions • Conduct pre-study visits and initiation visits • Provide input and have ideas valued to impact positive change for the company

🎯 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, which may constitute up to approximately 50-60% travel commitment • Fluency in English and for non-English speaking countries the local language of country where position based • Candidates must reside in Madrid or Barcelona • Please, apply in English only • 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

• High CRA retention rates and enjoyable quality of life • Lower than average number of protocols • Reasonable travel and improved work/life balance • Support from direct line management • Opportunity to have influence and impact • Employee input and ideas valued and nurtured