Clinical Research Associate – Oncology – West Coast – Remote
Posted 2025-08-26
Remote, USA
Part Time
Immediate Start
About the position
Responsibilities
• Manage the research activities at sites participating in Worldwide's clinical research projects, which are predominantly registries and other types of non-interventional / observational studies.
• Involved in all stages of the clinical study, including identifying potential sites to participate in the research effort.
• Perform various study start-up activities such as working with sites to collect appropriate regulatory documents and supporting the negotiation of contracts and budgets.
• Train the sites to collect data properly and report any potential safety-related events.
• Manage the site's activities during study maintenance.
• Close down research activities at the sites once the study has concluded.
• Conduct study initiation visits (SIVs).
• Ensure compliance with obtaining informed consent, reporting potential safety-related events, and adhering to all applicable regulatory requirements.
Requirements
• Excellent interpersonal, oral, and written communication skills in English.
• Superior organizational skills with attention to details.
• Ability to work with little or no supervision.
• 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 Oncology is required.
• Willingness to travel required.
Apply to This Job
Responsibilities
• Manage the research activities at sites participating in Worldwide's clinical research projects, which are predominantly registries and other types of non-interventional / observational studies.
• Involved in all stages of the clinical study, including identifying potential sites to participate in the research effort.
• Perform various study start-up activities such as working with sites to collect appropriate regulatory documents and supporting the negotiation of contracts and budgets.
• Train the sites to collect data properly and report any potential safety-related events.
• Manage the site's activities during study maintenance.
• Close down research activities at the sites once the study has concluded.
• Conduct study initiation visits (SIVs).
• Ensure compliance with obtaining informed consent, reporting potential safety-related events, and adhering to all applicable regulatory requirements.
Requirements
• Excellent interpersonal, oral, and written communication skills in English.
• Superior organizational skills with attention to details.
• Ability to work with little or no supervision.
• 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 Oncology is required.
• Willingness to travel required.
Apply to This Job