Senior Oncology CRA — Remote Site Lead & Trial Execution

Worldwide Clinical Trials; Durham (NC); Hybrid; USD 900,000 - 1,100,000; Full time

Job summary

Worldwide Clinical Trials is seeking a Clinical Research Associate (CRA) in the United States with oncology experience. You will oversee site management, regulatory submissions, and TMF processes, working with a global team to advance clinical research.

The role emphasizes travel regionally, strong communication, and collaboration with cross-functional teams. Candidates must reside in the United States and have 5+ years of CRA experience, with a 4-year degree or nursing background.

Qualifications

• Excellent interpersonal, oral, and written communication skills in English.
• Superior organizational skills with attention to detail.
• Ability to work with little or no supervision.
• Proficiency in Microsoft Office, CTMS, and EDC Systems.

Responsibilities

• Manage research activities at sites participating in Worldwide’s clinical research projects.
• Involved in study start-up activities, regulatory documents, and site training.
• Conduct study initiation visits (SIVs) and ensure regulatory compliance.
• Coordinate site activities remotely while maintaining informed consent and safety reporting.

Skills

English proficiency

Communication

Organizational skills

Self-motivation

MS Office

CTMS

EDC

Education

Bachelors degree or Nursing

Tools

CTMS

EDC

MS Office

Job description

Worldwide Clinical Trials is seeking a Clinical Research Associate (CRA) in the United States with oncology experience. You will oversee site management, regulatory submissions, and TMF processes, working with a global team to advance clinical research.

The role emphasizes travel regionally, strong communication, and collaboration with cross-functional teams. Candidates must reside in the United States and have 5+ years of CRA experience, with a 4-year degree or nursing background.