What is your mission? 

You will provide the best service to our partner brands by performing these tasks:

• Understand and comply with study protocols, ensuring accurate data collection and entry.
• Track study timepoints to ensure timely objective completion.
• Conduct internal audits for data completeness, validity, and accuracy.
• Perform data validation checks and monitor for missing or inconsistent entries.
• Test and validate new data forms and registries prior to launch.
• Input test data to support platform validation and ensure functionality.
• Manage patient follow-up processes, including communication and documentation.
• Maintain PHI security and adhere to HIPAA regulations.
• Collaborate with internal and external stakeholders to support data integrity and compliance.
• Other duties as assigned.

Who are we looking for?

• Bachelor’s degree in Life Sciences, Nursing, Pharmacy, or a related medical or scientific field.
• 1–2 years of experience in medical or drug coding within a clinical research or healthcare setting.
• Hands-on experience with MedDRA and WHODrug coding systems.
• Strong understanding of clinical data management and medical terminology.
• Knowledge of PHI security and HIPAA compliance.
• Proficiency in using clinical databases or EDC systems.
• Excellent attention to detail and commitment to data accuracy.
• Effective communication and collaboration skills with cross-functional teams.
• Positive work attitude and adaptability in a fast-paced research environment.