Expert Clinical Data Management Professional

1 day ago

Kolhapur, India beBeeEDC Full time

Job Title: Expert Clinical Data Management ProfessionalAbout the JobWe are seeking an experienced Clinical Data Management expert to join our team. As a key member of our clinical technology group, you will be responsible for designing and developing eCRF specifications, creating edit check specifications, implementing UAT scripts, and ensuring seamless integration of various modules within the EDC ecosystem.Key Responsibilities:eCRF Design and Development: Design and develop eCRF specifications for clinical trials, ensuring efficient setup processes.Edit Check Configuration: Create edit check specifications and configure edit checks at the trial level to maintain data integrity.UAT Script Implementation: Implement UAT scripts to test clinical study setups and ensure seamless integration.Study Setup and Management: Set up multiple instances of study URLs (e.g., UAT, production, testing) for streamlined management.User Account Management: Configure user accounts for study teams and manage access permissions accordingly.Blinded and Unblinded Study Configurations: Establish and manage blinded and unblinded study configurations to protect sensitive information.Subject Matter Expertise: Serve as the subject matter expert for EDC database-related activities, providing guidance and support.Module Integration: Integrate various modules within the EDC ecosystem, including coding, IRT, safety systems, and local labs, to enhance functionality.Custom Function Implementation: Understand when custom functions are required within EDC systems and implement them accordingly.Troubleshooting and Problem-Solving: Troubleshoot database setup issues and adapt solutions based on study needs.Post-Production Changes: Prepare, test, and implement post-production changes as needed to meet evolving study requirements.Requirements:Bachelor's degree in Computer Science, Information Technology, or related field.Minimum 5 years of experience in clinical data management, preferably with Veeva EDC.Strong understanding of eCRF design, edit check configuration, and UAT script implementation.Excellent problem-solving skills and ability to work independently.Effective communication and collaboration skills.Benefits:Competitive salary and benefits package.Ongoing training and professional development opportunities.Collaborative and dynamic work environment.Others:Please note that this is a unique opportunity to work with a leading organization in the clinical technology space. If you are passionate about clinical data management and want to make a meaningful contribution, we encourage you to apply.

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