Worldwide Clinical Trials
1001 - 5000 employees
🧬 Biotechnology
💊 Pharmaceuticals
⚕️ Healthcare Insurance
Biotechnology • Pharmaceuticals • Healthcare Insurance
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 Manager
🕒 June 5
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Worldwide Clinical Trials
1001 - 5000 employees
🧬 Biotechnology
💊 Pharmaceuticals
⚕️ Healthcare Insurance
Biotechnology • Pharmaceuticals • Healthcare Insurance
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
• Oversee, lead, manage, and provide technical expertise within the assigned projects to ensure they are executed efficiently, accurately, and timely. • Provide fully independent and autonomous leadership of data management services across multiple complex global projects/programs. • Ensure appropriate resources are allocated to complete all DM activities on time and within budget. • Prepare DM trial documentation (DMP, DB Specifications, Edit check specifications, CCGs, DTAs). • Write external vendor reconciliation specifications for programming reconciliation outputs. • Monitor project scope, budgets and risks and alert DM Management of any concerns.
🎯 Requirements
• Bachelor’s degree or higher in biomedical sciences, life sciences, computer science, or related discipline — or equivalent relevant experience. • Min of 5 years of experience in clinical data management or a related role within the pharmaceutical, biotechnology, or medical device industries. • Strong knowledge of data management best practices & technologies as applied to clinical trials. • Excellent communication and interpersonal skills to collaborate with cross-functional internal and external teams.
🏖️ Benefits
• Health insurance • Equal employment opportunities • Professional development opportunities • Flexible work environment
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