From our Health & Pharma Unit, we are looking for a Medical Content Specialist for a major multinational company. This is a temporary position based in CABA with a hybrid work model.
The Challenge
...
medical content specialist (i).
- ciudad autónoma de buenos aires
- posted 7 days ago
- closes 16 october 2026
job details
summary
- ciudad autónoma de buenos aires
- temporary
- job categoryhealth & social care, practitioner & technician
job details
As a Medical Content Specialist, you will be a key player in the medical review process, ensuring that all scientific and promotional materials meet the highest standards of accuracy and regulatory compliance. You will interact with diverse stakeholders across LATAM, acting as a technical bridge between Medical, Marketing, and Regulatory areas.
Key Responsibilities
- Medical review & approval: Lead the review and approval of promotional, non-promotional, and scientific materials. Ensure accuracy in translations, medical content, and compliance with local regulations.
- Scientific data interpretation: Accurately interpret clinical study data to support generated materials, ensuring a balanced view of product risks and benefits.
- Strategic alignment: Align medical content with marketing strategies and the promotional grid.
- Cross-functional collaboration: Partner with other areas inside the company.
- Process excellence: Identify process improvement opportunities, develop CAPAs when required, and ensure full compliance with governance principles.
- Expert oversight: Handle high-level technical and regulatory reviews.
Requirements
- Education: Medical Doctor (MD) or equivalent life science degree (Pharmacists, Biochemists, Nutritionists, Nurses).
- Experience: Minimum of 3 years of experience in the pharmaceutical industry or related sectors. Previous experience in medical review and regulatory affairs is highly valued.
- Languages: Advanced English (Oral and Written) is mandatory.
- Technical Knowledge: Strong understanding of clinical study results, risk/benefit profiles, and therapeutic area strategies. Familiarity with ANMAT regulations is a plus.
Working conditions
- Contract: Excellent contracting conditions through Randstad.
- Format: Hybrid (2 days in office / 3 days remote).
- Schedule: Monday to Thursday, 8:30 AM to 5:30 PM (flexible). Fridays until 2:00 PM.
- Location: CABA. Nos esforzamos todos los días en crear un entorno diverso y nos enorgullece ser una empresa con igualdad de oportunidades para todas las personas, independientemente de su raza, color, religión, sexo, identidad sexual u orientación sexual, país de origen, genética, discapacidad o edad.
show moreKey Responsibilities
- Medical review & approval: Lead the review and approval of promotional, non-promotional, and scientific materials. Ensure accuracy in translations, medical content, and compliance with local regulations.
- Scientific data interpretation: Accurately interpret clinical study data to support generated materials, ensuring a balanced view of product risks and benefits.
- Strategic alignment: Align medical content with marketing strategies and the promotional grid.
- Cross-functional collaboration: Partner with other areas inside the company.
- Process excellence: Identify process improvement opportunities, develop CAPAs when required, and ensure full compliance with governance principles.
- Expert oversight: Handle high-level technical and regulatory reviews.
Requirements
- Education: Medical Doctor (MD) or equivalent life science degree (Pharmacists, Biochemists, Nutritionists, Nurses).
- Experience: Minimum of 3 years of experience in the pharmaceutical industry or related sectors. Previous experience in medical review and regulatory affairs is highly valued.
- Languages: Advanced English (Oral and Written) is mandatory.
- Technical Knowledge: Strong understanding of clinical study results, risk/benefit profiles, and therapeutic area strategies. Familiarity with ANMAT regulations is a plus.
Working conditions
- Contract: Excellent contracting conditions through Randstad.
- Format: Hybrid (2 days in office / 3 days remote).
- Schedule: Monday to Thursday, 8:30 AM to 5:30 PM (flexible). Fridays until 2:00 PM.
- Location: CABA. Nos esforzamos todos los días en crear un entorno diverso y nos enorgullece ser una empresa con igualdad de oportunidades para todas las personas, independientemente de su raza, color, religión, sexo, identidad sexual u orientación sexual, país de origen, genética, discapacidad o edad.
From our Health & Pharma Unit, we are looking for a Medical Content Specialist for a major multinational company. This is a temporary position based in CABA with a hybrid work model.
The Challenge
As a Medical Content Specialist, you will be a key player in the medical review process, ensuring that all scientific and promotional materials meet the highest standards of accuracy and regulatory compliance. You will interact with diverse stakeholders across LATAM, acting as a technical bridge between Medical, Marketing, and Regulatory areas.
Key Responsibilities
- Medical review & approval: Lead the review and approval of promotional, non-promotional, and scientific materials. Ensure accuracy in translations, medical content, and compliance with local regulations.
- Scientific data interpretation: Accurately interpret clinical study data to support generated materials, ensuring a balanced view of product risks and benefits.
- Strategic alignment: Align medical content with marketing strategies and the promotional grid.
- Cross-functional collaboration: Partner with other areas inside the company.
...
- Process excellence: Identify process improvement opportunities, develop CAPAs when required, and ensure full compliance with governance principles.
- Expert oversight: Handle high-level technical and regulatory reviews.
Requirements
- Education: Medical Doctor (MD) or equivalent life science degree (Pharmacists, Biochemists, Nutritionists, Nurses).
- Experience: Minimum of 3 years of experience in the pharmaceutical industry or related sectors. Previous experience in medical review and regulatory affairs is highly valued.
- Languages: Advanced English (Oral and Written) is mandatory.
- Technical Knowledge: Strong understanding of clinical study results, risk/benefit profiles, and therapeutic area strategies. Familiarity with ANMAT regulations is a plus.
Working conditions
- Contract: Excellent contracting conditions through Randstad.
- Format: Hybrid (2 days in office / 3 days remote).
- Schedule: Monday to Thursday, 8:30 AM to 5:30 PM (flexible). Fridays until 2:00 PM.
- Location: CABA. Nos esforzamos todos los días en crear un entorno diverso y nos enorgullece ser una empresa con igualdad de oportunidades para todas las personas, independientemente de su raza, color, religión, sexo, identidad sexual u orientación sexual, país de origen, genética, discapacidad o edad.
show more- Expert oversight: Handle high-level technical and regulatory reviews.
Requirements
- Education: Medical Doctor (MD) or equivalent life science degree (Pharmacists, Biochemists, Nutritionists, Nurses).
- Experience: Minimum of 3 years of experience in the pharmaceutical industry or related sectors. Previous experience in medical review and regulatory affairs is highly valued.
- Languages: Advanced English (Oral and Written) is mandatory.
- Technical Knowledge: Strong understanding of clinical study results, risk/benefit profiles, and therapeutic area strategies. Familiarity with ANMAT regulations is a plus.
Working conditions
- Contract: Excellent contracting conditions through Randstad.
- Format: Hybrid (2 days in office / 3 days remote).
- Schedule: Monday to Thursday, 8:30 AM to 5:30 PM (flexible). Fridays until 2:00 PM.
- Location: CABA. Nos esforzamos todos los días en crear un entorno diverso y nos enorgullece ser una empresa con igualdad de oportunidades para todas las personas, independientemente de su raza, color, religión, sexo, identidad sexual u orientación sexual, país de origen, genética, discapacidad o edad.
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