Senior CRA | Home-based CNS Trials (Midwest)

Worldwide Clinical Trials

Lake Michigan Beach (MI)

Remote

USD 90,000 - 120,000

Full time

7 days ago
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Job summary

Worldwide Clinical Trials is seeking a Senior Clinical Research Associate to lead monitoring across CNS studies from sites in the Midwest. This home-based role requires travel and regional responsibilities to ensure protocol adherence, patient safety, and high-quality data throughout the trial lifecycle.

You will foster strong site relationships, train staff on protocol requirements, and collaborate with study teams and sponsors worldwide.

Qualifications

  • Bachelor’s degree or nursing degree required.
  • 5+ years as a regional traveling CRA.
  • Experience monitoring CNS clinical trials.
  • Strong knowledge of clinical trial processes, site management and regulatory requirements.

Responsibilities

  • Manage clinical research activities at investigative sites participating in Worldwide clinical studies.
  • Identify and assess potential research sites to support successful study execution.
  • Coordinate start-up activities including regulatory documentation and contract/budget support.
  • Conduct monitoring visits: PSSVs, SIVs, IMVs and COVs.
  • Train site personnel on protocol requirements, data collection, and safety reporting expectations.
  • Monitor site performance and provide ongoing support during study maintenance.
  • Ensure informed consent, safety reporting, and regulatory compliance.
  • Partner with sites and study teams to drive data quality and participant safety.
  • Support site closeout activities and complete study requirements.

Skills

Site management
Regulatory knowledge
CNS trials experience
Clinical trial processes
Traveling/Regional CRA

Education

Bachelor's Degree
Nursing Degree

Job description

Worldwide Clinical Trials is seeking a Senior Clinical Research Associate to lead monitoring across CNS studies from sites in the Midwest. This home-based role requires travel and regional responsibilities to ensure protocol adherence, patient safety, and high-quality data throughout the trial lifecycle.

You will foster strong site relationships, train staff on protocol requirements, and collaborate with study teams and sponsors worldwide.

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