Senior Clinical Data Coordinator

Job not on LinkedIn

🔥 6 minutes ago

🇮🇳 India – Remote

⏰ Full Time

🟠 Senior

✨ Clinical Data Coordinator

👻 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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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 Endpoint Adjudication Committee (EAC) activities, including case initiation, review, voting, and decision form distribution • Review and reconcile clinical trial data for completeness, accuracy, and protocol compliance • Manage adjudication case packets and ensure timely collection and submission of source documents • Generate, track, and resolve clinical data and adjudication-related queries • Prepare and maintain adjudication documents, forms, reports, listings, and study materials • Develop and maintain CRFs, data management plans, tracking logs, and study documentation • Perform data review, quality control, and data cleaning to ensure data integrity • Monitor case status, study metrics, and operational performance reporting • Serve as a liaison between sponsors, sites, committee members, vendors, and external stakeholders • Coordinate data transfers and exchanges with vendors, laboratories, and imaging review partners • Support the development and implementation of EAC processes, workflows, and operational tools • Ensure compliance with ICH-GCP, regulatory requirements, study protocols, and SOPs • Participate in study meetings, training activities, and cross-functional collaborations

🎯 Requirements

• Minimum Master's/Pharm D degree in any discipline; Life Sciences preferred • At least 4–6 years’ experience in Clinical Data Management or related industry experience in Pharmacovigilance, Clinical Research Coordinators, pharmaceutical or medical device companies • Strong organizational, communication, and time management skills • Knowledge of FDA, ICH and GCP guidelines as they apply to clinical studies and clinical data management • Experience with one or more Data Management/Data Collection Systems/Vendors; some EDC application experience preferred • Ability to function effectively in a fast-paced environment

🏖️ Benefits

• Employee employment status