Verification Associate
| Company | Suvoda |
|---|---|
| Location | Conshohocken, PA, USA |
| Salary | $Not Provided – $Not Provided |
| Type | Full-Time |
| Degrees | Bachelor’s |
| Experience Level | Junior, Mid Level |
Requirements
- Bachelor’s Degree or equivalent work experience and/or training
- 2+ 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
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
Preferred Qualifications
- 2+ years in the pharmaceutical or CRO industry preferred with contract management and/or data management related experience