Data Entry, Study Coordinator

Job not on LinkedIn

🔥 2 minutes ago

🇪🇸 Spain – Remote

⏰ Full Time

🟢 Junior

⬇️ Data Entry

👻 Ghost score 22%

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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Humaneva Group

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

🏥 Healthcare

💊 Pharmaceuticals

🤝 B2B

💰 $50M Private Equity Round - Humaneva on 2024-09

Healthcare • Pharmaceuticals • B2B

Humaneva Group is a clinical-research-focused organization that integrates patient care, scientific innovation, and data-driven approaches to provide reliable clinical research data to the medical community. The Group comprises three interrelated companies: a research site network, a contract research organization (CRO), and a technology platform that together create a connected data stream between patients, investigators, research centers, and data standards. Humaneva emphasizes integration of clinical operations with technology and appears to support therapeutic areas such as oncology, according to its site navigation.

📋 Description

• Coordinate the activities of clinical trials • Manage and maintain study documentation and records • Enter and review data in the trial’s electronic systems (eCRF) • Manage and resolve queries • Provide support during monitoring visits, audits and inspections • Ensure compliance with applicable procedures and regulations • Coordinate the dispatch and management of biological samples • Collaborate with investigators, CRAs, sponsors and other professionals involved in the study

🎯 Requirements

• A university degree in Health Sciences, Nursing, Pharmacy, Biology, Medicine or a related discipline • Previous experience in clinical research or similar roles within the healthcare sector • Minimum 6 months of experience; work placements count as experience • English language proficiency at B2 level or above • Strong organisational skills and the ability to prioritise • Attention to detail and a focus on quality • Communication and teamwork skills • A proactive attitude and a patient-centred approach • Specific training in clinical research is a plus • Knowledge of Good Clinical Practice (ICH-GCP) and the regulations applicable to clinical trials is a plus

🏖️ Benefits

• Be part of a leading international network in clinical research • Contribute directly to patients’ access to innovative treatments • Work alongside professionals with extensive experience in clinical research • Take part in studies across different therapeutic areas and innovative projects • Enjoy a collaborative, dynamic environment focused on professional development