Senior CRA – Oncology & Rare Disease (Remote-friendly)

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

Job summary

Worldwide Clinical Trials is seeking a Clinical Research Associate in the United States to manage site activities, ensure regulatory compliance, and support TMF processes. You’ll conduct study visits, coordinate with centralized teams, and help train sites. The role offers a clear career path, mentorship, and opportunities to contribute to global trials in oncology and rare disease.

5+ years CRA experience, fluent English, and willingness to travel regionally are required.

Qualifications

• Excellent interpersonal, oral, and written 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

• Responsible for managing the research activities at sites participating in Worldwide’s clinical research projects.
• Typically involved in all stages of the clinical study, including identifying potential sites to participate in the research effort, performing various study start‑up activities such as working with sites to collect appropriate regulatory documents and supporting the negotiation of contracts and budgets, training the sites to collect data properly and report any potential safety‑related events, managing the site’s activities during study maintenance, and closing down research activities at the sites once the study has concluded
• Conduct study initiation visits (SIVs)
• While most of the site management efforts will be performed remotely, you will be required to ensure compliance with obtaining informed consent, reporting potential safety‑related events, and adhering to all applicable regulatory requirements

Skills

English

Interpersonal skills

Organizational skills

Autonomy

Microsoft Office

CTMS

EDC Systems

Education

Universitary degree (4-year) or Nursing degree

Tools

Microsoft Office

CTMS

EDC Systems

Job description

Worldwide Clinical Trials is seeking a Clinical Research Associate in the United States to manage site activities, ensure regulatory compliance, and support TMF processes. You’ll conduct study visits, coordinate with centralized teams, and help train sites. The role offers a clear career path, mentorship, and opportunities to contribute to global trials in oncology and rare disease.

5+ years CRA experience, fluent English, and willingness to travel regionally are required.