Join the LLR family of private equity-backed growth companies.

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

Responsibilities

• 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

Qualifications

• Bachelor’s Degree or equivalent work experience and/or training
• Minimum of 3-4 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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