Medical Director – Rheumatology

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

📋 Description

• Oversees medical aspects of clinical trials to ensure adherence to SOPs, client instructions, and regulations.

• Participates in and presents at investigator and sponsor meetings.

• Offers medical consultation to clients, investigators, and project team members.

• Conducts medical reviews and analyses of serious adverse events in clinical trials and client deliverables.

• Ensures proper execution of tasks assigned to Pharmacovigilance (PV) in compliance with relevant regulations.

• Monitors all safety parameters of clinical studies.

• Engages in discussions regarding medical issues with principal investigators and clients.

• Manages signal detection activities and assists with updates to labels.

⛳️ Requirements

• An MD or equivalent is required.

• Active medical licensure is preferred.

• Clinical experience in patient treatment within the specialty or sub-specialty (approximately 2 years).

• Relevant clinical trial experience in a Contract Research Organization, pharmaceutical company, or as a principal investigator (around 1-2 years).

• Direct experience in safety/Pharmacovigilance (approximately 2 years).

• Strong decision-making, problem-solving, organizational, and analytical skills.

• Excellent verbal and written communication abilities.

• Familiarity with relevant safety databases (e.g., Medra).

• Willingness to travel both domestically and internationally.

• Proficiency in basic computer applications.

• Fluent in both spoken and written English.

• Capability to act as a mentor/trainer for other staff within the PV team.

🏝️ Benefits

• Health insurance.

• Retirement plans.

• Paid time off.

• Flexible working arrangements.

• Opportunities for professional development.

• Wellness programs.