Clinical Research Associate: Neurology & Oncology (Global)

Worldwide Clinical Trials; Germany (OH); On-site; USD 75,000 - 105,000; Full time

Job summary

Worldwide Clinical Trials is seeking a Clinical Research Associate (CRA) to work across therapeutic areas such as Neuroscience, Oncology, Cardiovascular, Metabolic and Rare Diseases. You will handle regulatory submissions, TMF management, and site management support with experienced colleagues.

You will monitor sites, mentor junior CRAs, and ensure protocol adherence, safety reporting and data quality across studies. Travel to sites is required, and a 4-year degree or RN/BSN is expected.

Qualifications

• Excellent interpersonal, oral, and written communication skills in English.
• Proficiency in Microsoft Office, CTMS and EDC Systems.
• 2+ years of experience as a Clinical Research Associate.
• 4-year university degree or RN/BSN in Nursing.
• Experience in Neurology, Oncology and Hematology is required.
• Willingness to travel.

Responsibilities

• Responsible for site qualification, initiation, interim monitoring, site management, and study close‑out visits.
• Provide mentoring and guidance to less experienced CRAs and site staff when needed.
• Document site visit findings via written reports.
• Assess, monitor, and train study site staff on protocol adherence as required.
• Review study subject safety information and informed consent.
• Conduct source document verification for compliance, patient safety, and veracity of data.
• Review CRFs using paper or electronic data capture systems and assist sites with data query resolution.
• Provide applicable updates for site‑related documentation for filing in the TMF.
• Ensure site compliance with IP receipt, accountability and return or destruction.
• Conduct accompanied site visits for assessment or training of other CRAs as requested and appropriate.

Skills

Interpersonal communication

Oral communication

Written communication

Microsoft Office

CTMS

EDC Systems

Education

4-year degree or RN/BSN

Tools

Microsoft Office

CTMS

EDC Systems

Job description

Worldwide Clinical Trials is seeking a Clinical Research Associate (CRA) to work across therapeutic areas such as Neuroscience, Oncology, Cardiovascular, Metabolic and Rare Diseases. You will handle regulatory submissions, TMF management, and site management support with experienced colleagues.

You will monitor sites, mentor junior CRAs, and ensure protocol adherence, safety reporting and data quality across studies. Travel to sites is required, and a 4-year degree or RN/BSN is expected.