On-Site Clinical Research Specialist — 2-Year Contract

Redbock - an NES Fircroft company; Minneapolis (MN); On-site; USD 70,000 - 90,000; Full time

Job summary

A leading clinical research firm is seeking a Clinical Research Specialist for a 24-month contract available on-site in Minneapolis, MN or Lafayette, CO. The role requires managing clinical evaluation studies, overseeing site operations, and ensuring compliance with Good Clinical Practices. Ideal candidates will possess a Bachelor's or higher degree, with a minimum of 2 years of relevant experience, specifically in site management and knowledge of clinical systems. This position offers a comprehensive approach to clinical trial management.

Qualifications

• Minimum 2 years of site management experience with a Bachelor's degree.
• 1+ years of experience required if holding an advanced degree.
• Strong knowledge of clinical practices and management systems.

Responsibilities

• Oversee and manage clinical evaluation research studies.
• Prepare protocols and patient record forms.
• Conduct clinical studies ensuring they meet medical needs.
• Interpret clinical investigation results for drug applications.
• Manage operational aspects of clinical trials aligning with regulations.
• Handle clinical supply operations and site/vendor selection.

Skills

Site Management experience

Knowledge of CTMS/EDC/TMF

Experience with Good Clinical Practice (GCP)

Experience with CTMS and patient data management systems

Experience with Microsoft Office Applications

Education

Bachelor's degree

Advanced degree

Tools

Veeva Vault

RAD Rave

Oracle

Job description

A leading clinical research firm is seeking a Clinical Research Specialist for a 24-month contract available on-site in Minneapolis, MN or Lafayette, CO. The role requires managing clinical evaluation studies, overseeing site operations, and ensuring compliance with Good Clinical Practices. Ideal candidates will possess a Bachelor's or higher degree, with a minimum of 2 years of relevant experience, specifically in site management and knowledge of clinical systems. This position offers a comprehensive approach to clinical trial management.