Senior CNS/Rare Disease CRA — Central U.S.

Worldwide Clinical Trials; Minnesota; On-site; USD 97,000 - 193,000; Full time

Benefits offered by this job

Competitive benefits package

Pay transparency

Job summary

Worldwide Clinical Trials is seeking an experienced Clinical Research Associate to oversee site activities across CNS/Neurology trials. The role emphasizes regulatory compliance, site training, and data integrity, with opportunities for career progression into Clinical Trial Management.

You will collaborate with cross-functional teams, travel regionally as needed, and participate in a transparent compensation framework.

Qualifications

• 5+ years of experience as a Clinical Research Associate.
• 4-year university degree OR Nursing Degree.
• Experience in CNS/Neurology and Rare Disease is required.
• Candidates must reside in the Central United States.
• Willingness to travel regionally required.

Responsibilities

• Manage the research activities at sites participating in Worldwide’s clinical research projects.
• Involve in all stages of the clinical study, including site identification, start-up activities, regulatory documents, contracts/budgets, training sites, data reporting, and safety event reporting.
• Conduct study initiation visits (SIVs).
• Ensure compliance with informed consent, safety reporting, and regulatory requirements, even when site activities are remote.

Skills

Interpersonal communication

Organizational skills

Independent work

MS Office

CTMS

EDC Systems

Education

Bachelors degree

Nursing Degree

Tools

CTMS

EDC Systems

MS Office

Job description

Worldwide Clinical Trials is seeking an experienced Clinical Research Associate to oversee site activities across CNS/Neurology trials. The role emphasizes regulatory compliance, site training, and data integrity, with opportunities for career progression into Clinical Trial Management.

You will collaborate with cross-functional teams, travel regionally as needed, and participate in a transparent compensation framework.