Worldwide Clinical Trials
1001 - 5000 employees
🏥 Healthcare
💼 Consulting
📦 Logistics
Healthcare • Consulting • Logistics
Worldwide Clinical Trials is a global contract research organization (CRO) that provides comprehensive clinical trial services. They specialize in supporting studies across diverse therapeutic areas such as oncology, cardiology, and rare diseases. With over 30 years of experience, Worldwide Clinical Trials emphasizes personalized support and customized solutions throughout the entire lifecycle of drug development. Their services include clinical monitoring, data management, patient recruitment, and regulatory consulting, ensuring precision and tailored attention for each clinical trial.
Clinical Data Management Associate II
🔥 1 minute ago
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Worldwide Clinical Trials
1001 - 5000 employees
🏥 Healthcare
💼 Consulting
📦 Logistics
Healthcare • Consulting • Logistics
Worldwide Clinical Trials is a global contract research organization (CRO) that provides comprehensive clinical trial services. They specialize in supporting studies across diverse therapeutic areas such as oncology, cardiology, and rare diseases. With over 30 years of experience, Worldwide Clinical Trials emphasizes personalized support and customized solutions throughout the entire lifecycle of drug development. Their services include clinical monitoring, data management, patient recruitment, and regulatory consulting, ensuring precision and tailored attention for each clinical trial.
📋 Description
• Manage ClinSpark, an electronic source system for Phase I clinical research • Design study databases, eSource systems, and electronic case report forms for data collection • Monitor, manage, quality-check, export, and archive clinical trial data and documents • Assist with database lock/unlock procedures and study building • Review study protocols and supporting documents • Attend study initiation visits and study planning meetings • Develop and update eSource databases, data management plans, database specifications, and eCRF guidelines • Perform verification and acceptance testing of configured databases • Perform medication and medical history coding • Identify and resolve data discrepancies and data integrity issues • Provide eSource system support and training to staff, monitors, and sponsor representatives • Liaise with internal and external data management or biostatistics teams • Manage the data collection library and participate in system upgrades and validation testing • Identify process improvements and provide recommendations to management • Present ClinSpark capabilities to prospective clients during bid defense and business development efforts • Plan and manage workload to meet study timelines and coordinate priorities with clinical staff • Request, schedule, and complete required training
🎯 Requirements
• Bachelor’s degree with at least three to five years of data management experience • Strong troubleshooting, error identification, and process-training ability • Ability to manage multiple tasks and deadlines in a fast-paced environment • Strong computer skills, including database management knowledge • Excellent written and oral communication skills • Comfortable presenting to internal and external stakeholders • Exceptional attention to detail • Knowledge of the clinical research process, including Good Clinical Practice • Familiarity with medical terminology • Previous supervisory experience managing small or large teams • Prior customer-facing experience required • Preferred: one to three years of clinical research experience • Preferred: three to five years of supervisory experience • Preferred: one to three years of general quality control experience • Data management certification and/or previous ClinSpark study design experience preferred • Must adhere to ICH-GCP guidelines and CDISC standards
🏖️ Benefits
• Competitive benefits package depending on location • Transparent compensation and pay equity • Salary information discussed during the interview process
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