Junior CRA – Argentina

Planet Pharma; Argentina; Presencial; ARS 900.000 - 1.300.000; Jornada completa

Descripción de la vacante

Planet Pharma is seeking a motivated Junior Clinical Research Associate to support LATAM operations in Argentina. You will assist in managing site activities, ensuring compliance with ICH-GCP and local regulations, and coordinating regulatory documentation.

The role involves site initiation, routine monitoring, and close-out visits, with travel within the region as needed. A degree in life sciences or healthcare is preferred and English fluency is required.

Formación

• 1 year of CRA experience in Argentina.
• Solid knowledge of ICH-GCP and local regulations.
• Experience with site management and monitoring.
• Willingness to travel within the region.

Responsabilidades

• Manage site activities and ensure regulatory compliance.
• Conduct site initiation, routine monitoring, and close-out visits.
• Maintain regulatory and Ethics Committee documentation.
• Foster investigator/site relationships and cross-functional collaboration.

Conocimientos

CRA experience Argentina

ICH-GCP knowledge

Site management & monitoring

Site initiation & close-out visits

Regulatory & Ethics documentation

Investigator/site relationship mgmt

Risk management & mitigation

Communication & organization

Stakeholder management

English fluency

Educación

Degree in life sciences/healthcare

Descripción del empleo

We expand our LATAM operations and make a meaningful impact in the world of clinical research. We are seeking a motivated and detail-oriented Junior Clinical Research Associate (CRA) to support our efforts in Argentina. This is an excellent opportunity for individuals looking to develop their career in clinical trials, working alongside experienced professionals in a dynamic and innovative environment.

In this role, you will be pivotal in managing site activities, ensuring compliance with international standards, and facilitating the seamless execution of clinical trials. Your contributions will help accelerate access to innovative therapies and improve patient outcomes worldwide. If you’re eager to grow your expertise in clinical research within a collaborative team that values excellence, this could be the perfect fit.

Required Skills:

• Proven experience working as a CRA in Argentina
• Strong knowledge of ICH-GCP guidelines and local clinical research regulations
• Hands‑on experience with site management and monitoring activities
• Ability to conduct site initiation, routine monitoring, and close‑out visits
• Experience in regulatory and Ethics Committee documentation
• Skilled in investigator/site relationship management
• Proactive risk management and mitigation strategies
• Excellent communication, organizational, and problem‑solving skills
• Strong stakeholder management and cross‑functional collaboration abilities
• Fluency in English (written and verbal)

Nice to Have Skills:

• Proficiency in Spanish (especially beneficial for Brazilian candidates)
• Experience in fast‑paced, global clinical trial environments

Preferred Education and Experience:

• A degree in life sciences, healthcare, or a related field is preferred
• Approximately 1 year of relevant CRA experience in Argentina

Other Requirements:

• Ability and willingness to travel as needed within the region
• Knowledge of local and international clinical research standards
• Commitment to ethical conduct and regulatory compliance