Review and interpret global customer documentation related to study activities, including but not
Identify areas of quality risk and/or need in pursuit of a best-in-class customer, site, and
Apply best practices to extract and configure customer data into applicable study activities from
Collaborate and communicate with business partners to verify interpretation of study requirements.
Adhere to auditing and monitoring checklists and procedures.
Adhere to both internal KPIs and customer-driven SLAs.

🎯 Requirements

At least 1 year of previous experience in the pharmaceutical or CRO industry with contract
Experience with Microsoft Word and Excel required
Strong attention to detail required
Ability to dissect the key elements of clinical trial financial documents and identify payable
Ability to handle high volume in a fast-paced environment
Excellent writing skills

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