Job Description
Job Title: Clinical Research Specialist Job ID: 22983
Duration: 24 Months Contract
Location: Mounds View, MN (Full-Time Onsite)
Pay Rate: $40/hr on W2
Job Summary: Medtronic is seeking a Clinical Research Specialist to support clinical study design, site management, data systems, and GCP-compliant trial execution. This role requires hands-on experience with clinical site oversight, CTMS/EDC/TMF systems, and daily operational management of clinical trials. The position is full-time onsite and contributes to protocol development, study management, and cross-functional project activities.
Key Responsibilities: - Oversee, plan, and support clinical evaluation studies
- Prepare protocols, forms, and documentation
- Manage clinical trial operations, site activities, and vendor coordination
- Ensure compliance with SOPs, GCP, and regulatory requirements
- Review and interpret clinical data
- Support clinical supply operations and site selection
- Work independently on moderately complex projects
Must-Have Skills & Requirements: - Minimum 2 years of clinical research or site management experience
- Strong site management experience (site or sponsor level)
- Hands-on experience with CTMS/EDC/TMF systems (Veeva Vault, RAD, Rave, Oracle, etc.)
- Working knowledge of Good Clinical Practice (GCP)
- Experience handling patient data and site documentation
- Proficiency in Microsoft Office applications
- Bachelor's degree in Life Sciences, Engineering, or related field
- Ability to work full-time onsite at the MN or CO location
Preferred: - Experience in clinical trial operations within medical device or pharmaceutical settings
- Ability to mentor junior team members
Job Tags
Full time, Contract work, Work at office,