Remote Clinical Research Specialist - 24-Month Contract

Redbock - an NES Fircroft company

United States

Remote

USD 55,000 - 75,000

Full time

2 days ago
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Job summary

Redbock - an NES Fircroft company is seeking a Clinical Research Specialist for a 24-month remote contract with a team based in Minnesota. The role supports planning and execution of clinical studies, including site management, documentation, data review, and stakeholder coordination.

The ideal candidate has 1-2+ years in clinical trials and site management, and will work under the Clinical Study Manager to ensure compliance with SOPs, GCP, and regulatory requirements across activities such as

Qualifications

  • 1-2+ years of clinical trial and site management experience.

Responsibilities

  • Oversees, designs, plans and develops clinical evaluation research studies.
  • Prepares and authors protocols and patient record forms.
  • Conducts registered and non-registered clinical studies of products that have been determined to satisfy a medical need and/or offer a commercial potential.
  • Oversees and interpret results of clinical investigations in preparation for new drug device or consumer application.
  • Oversees and resolves operational aspects of clinical trials in conjunction with project teams and in accordance with standard operating procedures (SOP), good clinical practice (GCP) and specific country regulations, and may prepare clinical trial budgets.
  • May be responsible for clinical supply operations, site, and vendor selection.

Skills

Site management
CTMS
EDC
TMF
GCP & Regulatory

Job description

Redbock - an NES Fircroft company is seeking a Clinical Research Specialist for a 24-month remote contract with a team based in Minnesota. The role supports planning and execution of clinical studies, including site management, documentation, data review, and stakeholder coordination.

The ideal candidate has 1-2+ years in clinical trials and site management, and will work under the Clinical Study Manager to ensure compliance with SOPs, GCP, and regulatory requirements across activities such as

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