CRA – ARGENTINA

Planet Pharma; Buenos Aires; Presencial; ARS 1.200.000 - 2.400.000; Jornada completa

Descripción de la vacante

Planet Pharma in Argentina is seeking a motivated Clinical Research Associate to support LATAM operations. The role focuses on site management, monitoring visits, and regulatory compliance in Argentina, with travel within the region and on-site collaboration with global teams.

The successful candidate will ensure ICH-GCP adherence, manage site relationships, and drive trial execution in a dynamic, collaborative environment, contributing to patient safety and data integrity.

Formación

• Proven CRA experience in Argentina with site management and monitoring.
• Strong knowledge of ICH-GCP and local regulations.
• Experience with regulatory and EC documentation.
• Experience in site initiation, visits and close-out activities.
• Excellent communication and stakeholder management skills.

Responsabilidades

• Manage site activities, monitoring and data integrity.
• Ensure compliance with ICH-GCP and local regulations.
• Conduct site initiation, routine monitoring and close-out visits.
• Prepare regulatory and Ethics Committee documentation.
• Cultivate investigator/site relationships and mitigate risks.

Conocimientos

CRA experience Argentina

ICH-GCP knowledge

Site management

Monitoring visits

Regulatory documentation

Investigator relationship

Risk management

Communication & org skills

Stakeholder management

English fluency

Educación

Bachelor's in life sciences

Descripción del empleo

CRA – Argentina

Location: Barcelona, Buenos Aires

Category: Clinical Development and Operations

Salary: Apply for details

Country: Argentina

Employment: Direct Hire/Perm

Worksite: On-Site

Job Description

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.

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

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 4 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

Equal Opportunity Employer

We are proud to be an equal opportunity employer. We welcome and encourage applications from all qualified candidates regardless of race, sex, gender identity or expression, disability, age, religion or belief, sexual orientation, or any other characteristic protected by applicable laws and regulations. It is our policy not to discriminate against any applicant or employee, and we are committed to fostering a diverse, inclusive, and respectful work environment across all locations in which we operate. We believe that diversity, equity, and inclusion are fundamental to our mission and enhance our ability to serve clients globally. If you have a disability or require any reasonable accommodations during the application or interview process, please inform your recruiter or contact us directly so that we can explore the appropriate arrangements.

Fraud Alert

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The Planet Group of Companies is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.