CRA – Argentina

Planet Pharma

Argentina

Presencial

ARS 45.349.000 - 81.628.000

Jornada completa

Hace 8 días
Generador de candidaturas

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Descripción de la vacante

Planet Pharma is expanding its LATAM operations and seeking a motivated Clinical Research Associate (CRA) to support clinical trials in Argentina. You will manage site activities, ensure compliance with ICH-GCP and local regulations, and drive the smooth execution of monitoring visits and regulatory submissions.

The role emphasizes site relationship management, risk mitigation, and cross-functional collaboration, with English fluency required.

Formación

  • 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).

Responsabilidades

  • Support LATAM operations and contribute to the execution of clinical trials.
  • Manage site activities ensuring compliance with international standards.
  • Facilitate timely initiation, monitoring, and close-out visits across sites.
  • Assist in regulatory submissions and Ethics Committee documentation.
  • Maintain investigator/site relationships and proactive risk mitigation.
  • Collaborate with cross-functional teams and communicate effectively.

Conocimientos

CRA experience in Argentina
ICH-GCP knowledge
Site management
Monitoring visits
Regulatory documentation
Investigator/site relationships
Risk management
Communication and problem-solving
Stakeholder collaboration
English fluency

Educación

Life sciences degree
4 years CRA experience in Argentina

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 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 4year 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

This is your chance to be part of a dedicated global team committed to innovation, excellence, and making a difference.

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