Senior Clinical Research Associate - Rare Diseases

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

Job summary

Worldwide Clinical Trials is seeking a seasoned Clinical Research Associate (CRA) to support site management across diverse therapeutic areas, including Rare Diseases and Oncology. You will collaborate with sites, ensure regulatory compliance, collect essential documents, and assist with contracts and budgets.

The role emphasizes remote site oversight, travel regionally, and a clear path to more senior clinical operations leadership.

Qualifications

• 5+ years of CRA experience.
• Experience in Rare Disease or Oncology required.
• Must reside on East Coast or Central United States.
• Willingness to travel regionally.

Responsibilities

• Manage research activities at sites participating in Worldwide’s clinical research projects.
• Involve in all stages of the clinical study, including site identification, start-up docs, contracts/budgets, training, and site maintenance.
• Conduct study initiation visits (SIVs).
• Ensure regulatory compliance, informed consent, and safety reporting across sites.

Skills

Communication in English

Organizational skills

Independent / self-directed

Microsoft Office, CTMS, EDC

Education

4-year degree or nursing

Tools

CTMS

EDC Systems

Job description

Worldwide Clinical Trials is seeking a seasoned Clinical Research Associate (CRA) to support site management across diverse therapeutic areas, including Rare Diseases and Oncology. You will collaborate with sites, ensure regulatory compliance, collect essential documents, and assist with contracts and budgets.

The role emphasizes remote site oversight, travel regionally, and a clear path to more senior clinical operations leadership.