Clinical Data Specialist

3 weeks ago


Minneapolis, Minnesota, United States GForce Life Sciences Full time

Clinical Data Coordinator Job Summary

At GForce Life Sciences, we are seeking a highly skilled Clinical Data Coordinator to oversee data management activities for clinical studies. As a key member of our team, you will ensure the integrity of study data by entering, reviewing, modifying, reconciling, and organizing data. This role requires working onsite and involves testing and verifying clinical data management systems, managing discrepancies, and complying with FDA regulations.

Key Responsibilities:

• Develop and maintain Case Report Forms and Edit Check specifications
• Create and update Data Management Plans
• Perform data quality checks and manage discrepancies (creating, routing, and resolving)
• Analyze data and prepare reports, with intermediate-level knowledge of Excel functions such as pivot tables, search functions, and XLOOKUP
• Test database setups and Edit Check programming
• Handle external data and device reconciliation
• Participate in Post Market Surveillance reporting as needed
• Ensure compliance with FDA regulations, ICH guidelines, ISO 14155, and company policies

Qualifications:

• Minimum of 2 years in a comparable or closely related clinical research environment. 1 year of experience may be considered if all other requirements are met. Medical device experience is a plus.
• Proficiency in computer skills, including Excel (pivot tables, search functions, XLOOKUP)
• Ability to manage multiple projects
• Experience with clinical databases (Oracle preferred but not required)

If you are a detail-oriented and organized individual with a passion for data management, we encourage you to apply for this exciting opportunity to join our team at GForce Life Sciences.



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