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,

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