Job Description

Job Location: 100% remote from Romania

Recruitment process:

• HR discussion
  
• Technical interview

The Verification Associate's primary role entails verifying that data is accuratelyconfigured prior to being uploaded into the software to allow for payment to the intended parties.

• Perform quality review on system configurations completed internally to ensure that data is extracted accurately from the contract, budget, or informed consent prior to being uploaded into the software
• Ensure that client specifications are met during implementation within configurations
• Establish auditing and monitoring checklists and procedures
• Ensure compliance in process and appropriate documentation is captured
• Collaborate internally to design, develop, and deliver a training program to support the configuration process
• Collaborate internally as needed to produce metrics and analytics to identify gaps in process, training, etc.
• Perform other duties, assignments, and/or special projects as time or circumstances necessitate

Profile:

• 2-5 years in the pharmaceutical or CRO industry preferred with contract management and/or data management related experience
• Foundational background on global clinical trial design, contracts and budget
• Ability to understand and interpret global clinical contracts, budgets, amendments, and informed consents
• Ability to dissect the key elements of trial budgets, including therapeutic phase and country-specific variances
• Ability to handle high volume of contract activity in a fast-paced environment with attention to detail
• Excellent writing skills Must have excellent analytical, organizational, interpersonal and time management skills
• Experience with Microsoft Word and Excel - required.