Senior Clinical Research Associate

This is a fully remote position, open to applicants in Argentina.

📋 Description

• Oversee research operations at sites involved in Worldwide's clinical research initiatives.

• Assist in all phases of clinical trials, from identifying potential sites to executing study start-up tasks.

• Gather necessary regulatory documentation from participating sites.

• Facilitate the negotiation of contracts and budgets.

• Educate sites on accurate data collection and the reporting of safety-related incidents.

• Supervise site activities throughout the maintenance phase of the study.

• Finalize research operations at sites upon the conclusion of studies.

• Conduct study initiation visits (SIVs).

• Ensure adherence to informed consent, safety-event reporting, and relevant regulatory standards.

⛳️ Requirements

• Exceptional interpersonal, verbal, and written communication abilities in English.

• Strong organizational skills with a keen attention to detail.

• Capability to work independently with minimal supervision.

• Proficient in Microsoft Office, CTMS, and EDC Systems.

• A minimum of 5 years of experience as a Clinical Research Associate.

• Bachelor's degree or a Nursing degree.

• Experience in Oncology is mandatory.

• Fluency in both written and spoken English is essential.

• Candidates must be residents of Argentina.

• Willingness to travel within the region is required.

🏝️ Benefits

• A diverse and inclusive workplace.

• Supportive and collaborative teams.

• Accessible and hands-on leadership.

• Equal employment opportunities for all.