Senior Oncology CRA – Remote Site Mgmt (Midwest/Central)

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

Job summary

Worldwide Clinical Trials is seeking a Clinical Research Associate to join our global CRO team. You will contribute across cardiovascular, metabolic, neuroscience, oncology, and rare diseases, with a focus on site management and regulatory support.

Requirements include 5+ years CRA experience, a 4-year degree or nursing degree, oncology experience, residency in the Midwest or Central regions, and willingness to travel regionally.

Qualifications

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

Responsibilities

• Manage research activities at sites participating in Worldwide’s clinical research projects.
• Involves identifying potential sites, start-up activities, regulatory documents, contracts and budgets, data collection training, and reporting safety events.
• Conduct study initiation visits (SIVs).
• Ensure compliance with informed consent and regulatory requirements, most site management is remote

Skills

Communication skills

Organizational skills

Independent work

Education

4-year bachelor’s degree

Nursing degree

Tools

Microsoft Office

CTMS

EDC Systems

Job description

Worldwide Clinical Trials is seeking a Clinical Research Associate to join our global CRO team. You will contribute across cardiovascular, metabolic, neuroscience, oncology, and rare diseases, with a focus on site management and regulatory support.

Requirements include 5+ years CRA experience, a 4-year degree or nursing degree, oncology experience, residency in the Midwest or Central regions, and willingness to travel regionally.