Senior CRA - CNS Trials | Remote Midwest Travel

Worldwide Clinical Trials; United States; Remote; USD 97,000 - 193,000; Full time

Job summary

Worldwide Clinical Trials is seeking a Senior Clinical Research Associate to lead site monitoring and ensure data integrity across studies in the Midwest United States. You will travel regularly (8–10 days per month) and oversee activities from site qualification through closeout, collaborating with global teams.

You will work with investigative sites, sponsors, and study teams to drive data quality, patient safety, and study success while ensuring protocol adherence and regulatory compliance.

Qualifications

• Bachelor’s Degree or a Nursing Degree required.
• 5+ years as a regional traveling Clinical Research Associate.
• Required CNS clinical trials monitoring experience.
• Willingness to travel within the Midwest region; 8–10 days per month.
• Experience in full-service monitoring preferred.

Responsibilities

• Manage clinical research activities at investigative sites participating in Worldwide clinical studies.
• Identify and assess potential research sites to support study execution.
• Coordinate study start-up activities including regulatory documentation and contract/budget support.
• Conduct monitoring visits (PSSVs, SIVs, IMVs, COVs).
• Train site personnel on protocols, data collection, and safety reporting expectations.
• Monitor site performance and provide ongoing support throughout study maintenance.

Skills

CRA experience

Site management

Regulatory knowledge

Travel willingness

CNS trials experience

Education

Bachelor’s or Nursing degree

Job description

Worldwide Clinical Trials is seeking a Senior Clinical Research Associate to lead site monitoring and ensure data integrity across studies in the Midwest United States. You will travel regularly (8–10 days per month) and oversee activities from site qualification through closeout, collaborating with global teams.

You will work with investigative sites, sponsors, and study teams to drive data quality, patient safety, and study success while ensuring protocol adherence and regulatory compliance.