Senior Oncology CRA: Lead Site Operations & Trials

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

Job summary

Worldwide Clinical Trials is seeking a seasoned Clinical Research Associate to join our Clinical Operations team in the Central United States. You will oversee site activities, support regulatory submissions, TMF management, and ensure data integrity across multiple therapeutic areas, with a focus on Oncology.

Ideal candidates bring 5+ years of CRA experience, a 4-year degree or nursing credential, and the ability to travel regionally.

Qualifications

• 5+ years of experience as a Clinical Research Associate.
• 4-year university degree or Nursing degree.
• Experience in Oncology.
• Candidates must reside in the Central United States.
• Willingness to travel regionally.

Responsibilities

• Manage research activities at sites participating in Worldwide’s clinical research projects.
• Involved in all stages of the clinical study, including site startup activities, regulatory documents, and contracts/budgets.
• Train sites to collect data properly and report any potential safety-related events.
• Manage the site’s activities during study maintenance and close-down.
• Conduct study initiation visits (SIVs).
• Ensure compliance with informed consent and regulatory requirements.

Skills

English communication

Organizational skills

Self-motivation

Education

4-year university degree or Nursing degree

Tools

Microsoft Office

CTMS

EDC Systems

Job description

Worldwide Clinical Trials is seeking a seasoned Clinical Research Associate to join our Clinical Operations team in the Central United States. You will oversee site activities, support regulatory submissions, TMF management, and ensure data integrity across multiple therapeutic areas, with a focus on Oncology.

Ideal candidates bring 5+ years of CRA experience, a 4-year degree or nursing credential, and the ability to travel regionally.