Medical Content Specialist (i)

Randstad Argentina; Victoria; Híbrido; ARS 1.200.000 - 1.800.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Contract via Randstad

Hybrid work model

Descripción de la vacante

Randstad Argentina is seeking a Medical Content Specialist for a major multinational company. This temporary position is based in CABA with a hybrid work model (2 days in office, 3 days remote).

You will lead medical review and regulatory checks of promotional and scientific materials, interpret clinical data, and align content with marketing strategies while collaborating with Medical, Marketing and Regulatory teams across LATAM.

Formación

• MD or life science degree required
• Minimum 3 years in pharmaceutical industry or related sectors
• Advanced English (oral and written) mandatory
• Familiarity with local regulations (ANMAT a plus)

Responsabilidades

• Medical review & approval: lead review/approval of promotional and scientific materials and translations
• Interpret clinical study data to support materials
• Align medical content with marketing strategies and promotional grid
• Collaborate with Medical, Marketing and Regulatory teams across LATAM
• Identify opportunities to improve processes and ensure governance compliance
• Provide expert oversight on high-level technical and regulatory reviews

Conocimientos

Medical content review

Regulatory compliance

English proficiency

Stakeholder management

Cross-functional collaboration

Clinical data interpretation

Educación

MD or life science degree

Descripción del empleo

From our Health & Pharma Unit, we are looking for aMedical Content Specialistfor 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.

educación

Universitario completo