Senior Clinical Research Associate – Global Site Management

Worldwide Clinical Trials; California; Remote; USD 70,000 - 110,000; Full time

Job summary

Worldwide Clinical Trials is seeking a Clinical Research Associate to join our global CRO, supporting site management across therapeutic areas from cardiovascular to oncology. You will coordinate regulatory documents, training, budgets, and data collection with remote collaboration.

We value independence, strong English communication, travel regionally, and a clear path to clinical trial management. The company emphasizes pay transparency and equal opportunity employment for a diverse workforce.

Qualifications

• Excellent interpersonal, oral, and written communication skills in English.
• Ability to work with little or no supervision.
• Proficiency in Microsoft Office, CTMS, and EDC Systems.
• 5+ years of experience as a Clinical Research Associate.
• ~4-year university degree OR Nursing Degree.
• ~ Experience in CNS/Neurology OR Rare Disease are required.
• ~ Willingness to travel regionally required.

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.
• 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

Interpersonal skills

Oral communication

Written communication

Independence

Microsoft Office

CTMS

EDC Systems

Willingness to travel

Education

4-year university degree

Nursing degree

Tools

CTMS

EDC Systems

Microsoft Office

Job description

Worldwide Clinical Trials is seeking a Clinical Research Associate to join our global CRO, supporting site management across therapeutic areas from cardiovascular to oncology. You will coordinate regulatory documents, training, budgets, and data collection with remote collaboration.

We value independence, strong English communication, travel regionally, and a clear path to clinical trial management. The company emphasizes pay transparency and equal opportunity employment for a diverse workforce.