What is your mission? 

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

• Understand and comply with study protocols: Effectively utilize available resources; Use appropriate methods for quality survey conduct and quality assurance measures for accurate data collection and entry.
• Adhere to protocols for internal audits on data completeness, validity and accuracy.
• Perform data validation checks monitoring for missing data as well as data entry discrepancies.
• Perform validation and user functionality checks on newly created forms prior to those forms going live in a database.
• Perform UAT on new registries and platforms prior to those going live in the database.
• Input tester data to enable project validation.
• Adhere to protocols for internal audits on data completeness, validity and accuracy. 
• Other duties as assigned.
• Accurately track current timepoints to ensure timely completion of study objectives.

Who are we looking for?

• At least 1 to 2 years of experience in data coordination or data management.
• Clinical trial data management experience.
• Knowledge of medical terminology.
• Experience with PHI security (HIPAA).
• Strong attention to detail and high accuracy in data entry and coding.
• Excellent verbal and interpersonal communication skills, with strong English writing skills.
• Ability to work independently and complete tasks and projects with minimal supervision.
• Strong problem-solving skills and a keen eye for detail.
• Ability to manage multiple priorities and meet deadlines effectively.
• Available to start ASAP.