Senior Clinical Research Associate - Oncology - Midwest/Central

Worldwide Clinical Trials; Springfield (IL); On-site; USD 97,000 - 193,000; Full time

Job summary

Worldwide Clinical Trials is seeking a Senior Clinical Research Associate to manage oncology trial sites across the Midwest and Central regions. You will oversee site identification, initiation visits, and regulatory compliance while coordinating with study teams.

The ideal candidate has 5+ years of CRA experience, a 4-year degree or nursing degree, oncology experience, and proficiency with MS Office, CTMS, and EDC systems. Willingness to travel regionally is essential.

Qualifications

• 5+ years clinical research associate experience.
• 4-year university degree or nursing degree required.
• Oncology experience required.
• Proficiency in Microsoft Office, CTMS, and EDC systems.
• Excellent written and oral communication skills.
• Superior organizational skills and attention to detail.
• Must reside in Midwest or Central regions and be willing to travel.

Responsibilities

• Manage research activities at participating study sites
• Conduct site identification, initiation visits, and contract negotiations
• Train sites on data collection and safety event reporting procedures
• Monitor site compliance with regulatory requirements and informed consent
• Oversee site activities during maintenance and study closeout phases

Skills

Clinical Research Experience

Communication skills

Organizational skills

Oncology Experience

Travel readiness

Education

Bachelor's degree or Nursing degree

Tools

Microsoft Office

CTMS

EDC systems

Job description

Worldwide Clinical Trials seeks a Senior Clinical Research Associate to manage oncology trial sites across the Midwest and Central regions. The role involves site selection, study initiation, regulatory compliance, and remote site monitoring with periodic regional travel.

Responsibilities

• Manage research activities at participating study sites
• Conduct site identification, initiation visits, and contract negotiations
• Train sites on data collection and safety event reporting procedures
• Monitor site compliance with regulatory requirements and informed consent
• Oversee site activities during maintenance and study closeout phases

Requirements

• 5+ years clinical research associate experience
• 4-year university degree or nursing degree
• Oncology experience required
• Proficiency in Microsoft Office, CTMS, and EDC systems
• Excellent written and oral communication skills
• Superior organizational skills and attention to detail
• Reside in Midwest or Central regions; willingness to travel

Compensation: $97,000-$193,000 annually