Senior CRA - CNS & Rare Disease | Growth Path

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

Job summary

Worldwide Clinical Trials is seeking a seasoned Clinical Research Associate (CRA) based in the Midwest to support site management across diverse therapeutic areas. You'll collaborate with cross-functional teams to drive accurate data collection, regulatory submissions, and safety reporting throughout the study lifecycle.

The role emphasizes hands-on site management, regulatory compliance, and professional development within a supportive team culture. Travel regionally is required.

Qualifications

• 5+ years of experience as a Clinical Research Associate.
• 4-year university degree or Nursing degree.
• Experience in Rare Disease and CNS is required.
• Candidates must reside in the Midwest.
• Willingness to travel regionally required.

Responsibilities

• Manage research activities at sites participating in Worldwide’s clinical research projects.
• Involved in all stages of the clinical study, including site initiation, regulatory document collection, contract and budget support, training sites, and safety reporting, with study closeout.
• Conduct study initiation visits (SIVs).
• Ensure compliance with informed consent, safety reporting, and regulatory requirements.

Skills

Interpersonal communication

Organizational skills

Independent work

MS Office, CTMS, EDC

Education

Bachelor's degree or Nursing degree

Tools

CTMS

EDC

Microsoft Office

Job description

Worldwide Clinical Trials is seeking a seasoned Clinical Research Associate (CRA) based in the Midwest to support site management across diverse therapeutic areas. You'll collaborate with cross-functional teams to drive accurate data collection, regulatory submissions, and safety reporting throughout the study lifecycle.

The role emphasizes hands-on site management, regulatory compliance, and professional development within a supportive team culture. Travel regionally is required.