Job Location: 100% remote from Romania
Recruitment process:
- HR discussion
- Technical interview
Role description:
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.
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