Medical Director – Cardiology

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

📋 Description

• Oversee all medical responsibilities related to contracted tasks throughout the pharmaceutical product life-cycle.

• Offer medical consultation to team members and address all study-related medical inquiries.

• Deliver therapeutic and protocol training for assigned studies upon request.

• Assist in drafting (interpreting safety and efficacy data) and/or reviewing CSR, IND/NDA reports, ICSR, signal detection reports, periodic reports, RMP, REMS, CTD modules, etc., to ensure accuracy and completeness of medical content.

• Track all safety variables (AE, laboratory abnormalities, changes in patient medical status).

• Discuss all medical issues with principal investigators and clients.

• Conduct medical reviews of adverse events of special interest, serious adverse events, and clinical outcomes events reported by study sites.

⛳️ Requirements

• MD or equivalent is required.

• Clinical experience in treating patients in the relevant specialty or sub-specialty associated with the applicant's training (approximately 2 years).

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

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

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

• Proficient in spoken and written English.

🏝️ Benefits

• Flexible work arrangements.

• Professional development opportunities.