What is your mission? 

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

• Understand and comply with study protocols, utilizing available resources effectively.

• Apply appropriate methods for quality survey conduct and assurance to ensure accurate data collection and entry.

• Accurately track current timepoints to support timely completion of study objectives.

• Adhere to protocols for conducting internal audits on data completeness, validity, and accuracy.

• Perform data validation checks, monitoring for missing data and discrepancies in data entry.

• Conduct validation and user functionality checks on newly created forms before they go live in the database.

• Perform user acceptance testing (UAT) on new registries and platforms prior to deployment.

• Input tester data to support project validation.

• Perform other duties as assigned.

Who are we looking for?

• 2–3 years of experience in medical coding and drug coding

• Experience with clinical trial data management

• Familiarity with medical terminology

• Knowledge and understanding of PHI security standards (HIPAA compliance)

• Familiarity with coding systems such as MedDRA and WHO Drug