Senior Clinical Research Associate

🕒 September 21

🇪🇸 Spain – Remote

⏰ Full Time

🟠 Senior

🧪 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 studies are conducted, recorded, and reported according to protocol, SOPs, ICH-GCP, applicable regulations and standards • Coordinate study setup and monitoring activities, including investigator identification, regulatory submissions, pre-study visits and initiation visits • Handle appropriately sized clinical trials • Support larger clinical study teams • 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 • Holder of CRA certificate • Minimum 5 years of CRA/SCRA experience within a CRO, pharmaceutical, biotechnology, or medical device environment • Extensive experience in IVD (In Vitro Diagnostics), oncology, infectious diseases and gastrointestinal studies • Proven experience monitoring studies across multiple European countries • Availability for domestic travel including overnight stays, up to approximately 50–60% travel commitment • International travel may be required for some senior-level positions • Fluency in Spanish and English is required • Apply in English

🏖️ Benefits

• Employees are empowered to make an impact • Meaningful client relationships • Career growth opportunities • Professional development • Collaborative and quality-focused environment • Equal opportunity employer • Reasonable accommodation available during the application process