Venesco, LLC

Medical Coder Location: Remote/Hybrid Job Type: Full-Time Position Overview Venesco is seeking a detail-oriented Medical Coder to support clinical trials through accurate coding and reconciliation of medical data. Key Responsibilities Code medical terminology using MedDRA and WHO Drug dictionaries Ensure consistency and quality of coded clinical trial data Review case report forms (CRFs) for accuracy Maintain coding conventions and documentation Generate coding reports and support data reconciliation activities Minimum Qualifications Bachelor’s degree in life sciences or related field 3–5 years of medical coding experience Knowledge of MedDRA and WHO Drug coding systems Preferred Qualifications Medical coding certification Experience supporting clinical trials #J-18808-Ljbffr

Venesco, LLC is seeking a detail-oriented Medical Coder to support clinical trials from a remote/hybrid location. The role involves coding medical terminology using MedDRA and WHO Drug dictionaries, ensuring the quality of coded clinical data, and reviewing case report forms for accuracy. Candidates should have a Bachelor’s degree in life sciences and 3–5 years of experience in medical coding. Preferred qualifications include medical coding certification and experience with clinical trials. #J-18808-Ljbffr

Venesco, LLC is seeking a Medical Coder to perform clinical coding activities for adverse events, medical histories, procedures, and concomitant medications for FDA-regulated clinical trials, ensuring accuracy and regulatory compliance. The ideal candidate will hold MedDRA and WHO-Drug certifications, have at least 7 years of medical coding experience, and be proficient with MedDRA and dictionaries. You will develop coding conventions, review CRFs, support data review and regulatory submissions. #J-18808-Ljbffr

Description Medical Coder Venesco LLC is seeking a Medical Coder to perform clinical coding activities for adverse events, medical histories, procedures, and concomitant medications for FDA-regulated clinical trials, ensuring consistency, accuracy, and regulatory compliance. Requirements Duties and Responsibilities Code adverse events using MedDRA terminology. Code medications using WHO Drug Dictionary. Develop coding conventions and coding guidelines. Review CRFs and contribute to data review activities. Perform coding reconciliation activities. Generate coding reports and quality control reviews. Support database testing and validation activities. Conduct coding-related training for study personnel. Maintain coding documentation and audit trails. Support regulatory submissions and database lock activities. Minimum Qualifications Bachelor's degree in Health Sciences, Clinical Research, Nursing, Pharmacy, or related discipline. MedDRA Certified and WHO-Drug Certified. Minimum 7...