To discuss more about this job opportunity, please reach out to Chitrank Rastogi (LinkedIn URL - https://www.linkedin.com/in/chitrank-rastogi-55119a102/), email your updated resume at Email - chitrank.rastogi@collabera.com or give me a call at (425) 523-1648. Thank you!

Job Description:
Job Roles & Responsibilities:

• 100% Onsite Role will ensure the integrity of study data by entering, reviewing, modifying, reconciling, and organizing data Testing and verification of clinical data management systems
• Discrepancy management (creating, routing, and resolving) Comply with FDA regulations
• Develop and maintain positive and trusting relationships with all levels of employees and customers
• A continuous Improvement mindset Will identify potential issues, this is very repetitive work
• Data will be studied and analyzed in Excel format so knowledge of pivot tables, search functions, and x-lookups is required at an intermediate level
• Nice to have - Medical Device experience Will need to have a minimum of 2 years of experience: comparable or closely related clinical research environment; HM is not opposed to 1 year of experience if all of the other requirements are met.

Education:

• H. S. Diploma or GED is required - will accept college graduates with at least one year of experience

Top Skills Needed:

• Strong communication - verbal and written
• Organizational skills
• Strong attention to detail
• Strong computer skills
• Ability to manage multiple projects.
• Prior experience working with Clinical Database Management Systems is preferred.