**Clinical Project Manager (CPM) / Drive Excellence in Clinical Research!**
Are you a seasoned clinical trial leader with expertise in LATAM regulations? Ready to make an impact in global drug development? This is your opportunity to lead groundbreaking clinical research!
**About the Company**
Our client is a leading clinical research organization (CRO) transforming the clinical trial landscape. Partnering with global biopharma companies, investigators, and healthcare institutions, they drive cost-effective, high-quality trials that bring life-changing therapies to market. With a strong footprint in Latin America, they ensure regulatory excellence and accelerated drug development.
**Your Role**
- Oversee clinical trials from initiation to completion, ensuring seamless execution
- Ensure compliance with ICH/GCP guidelines and LATAM regulatory bodies (COFEPRIS, ANVISA, INVIMA, DIGEMID)
- Manage budgets, vendors, and stakeholders, optimizing trial efficiency
- Act as the key liaison with sponsors and cross-functional teams
- Proactively identify risks and implement mitigation strategies
- Support the development of Clinical Study Reports (CSRs)
What You Bring
- Bachelor’s degree in Life Sciences or a related field




- 4+ years of experience managing clinical trials in biopharma or CRO environments
- Proven track record in LATAM regulatory submissions & compliance
- Strong leadership and project management skills
- Expertise in EDC and eTMF platforms (Veeva or similar)
- In-depth knowledge of LATAM regulatory agencies (COFEPRIS, ANVISA, INVIMA, DIGEMID)
Why Join Us?
- Be part of a fast-growing, innovative organization
- Work on cutting-edge treatments addressing unmet medical needs
- Collaborate with top industry professionals
- Competitive salary & benefits
Tipo de puesto: Tiempo completo
Sueldo: $80,000.00 - $90,000.00 al mes
Beneficios:
- Aumentos salariales
- Descuento de empleados
- Días de maternidad superiores a los de la ley
- Días de paternidad superiores a los de la ley
- Días por enfermedad
- Horarios flexibles
- Opción a contrato indefinido
- Seguro de gastos médicos
- Confiable de gastos médicos mayores
- Seguro de vida
- Trabajo desde casa
- Vacaciones adicionales o permisos con goce de sueldo
- Vales de despensa
Pago complementario:
- Bono de productividad
Tipo de jornada:
- Lunes a viernes
- Turno de 8 horas
Lugar de trabajo: Empleo presencial

📌 Clinical Project Manager (Cpm) / Clinical Trials (Polanco)
🏢 Otos Group para un Cliente CRO
📍 Polanco