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.

• Identify potential sites for participation in research activities.

• Execute study start-up tasks, which include gathering regulatory documents from sites.

• Assist in negotiating contracts and budgets.

• Provide training to sites on proper data collection and reporting of safety-related events.

• Manage site operations throughout the study maintenance phase.

• Conclude research activities at sites following the completion of the study.

• Conduct study initiation visits (SIVs).

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

⛳️ Requirements

• Exceptional interpersonal, oral, and written communication skills in English.

• Strong organizational abilities with a keen attention to detail.

• Capability to work independently with minimal supervision.

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

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

• Bachelor’s degree or Nursing Degree required.

• Experience in Oncology is mandatory.

• Fluent in written and spoken English is essential.

• Candidates must be residents of Argentina.

• Willingness to travel regionally is necessary.

🏝️ Benefits

• A diverse and inclusive workplace.

• Supportive and collaborative teams.

• Accessible leadership.

• Opportunities for professionals from various backgrounds and experiences to thrive.

• Equal employment opportunities.

• Regional travel opportunities.