Clinical Research Associate II or Sr- Argentina

Parexel; Argentina; Remote; ARS 90,873,000 - 136,310,000; Full time

Benefits offered by this job

Home-based role

Buenos Aires preference

Job summary

Parexel is seeking an experienced Clinical Research Associate II/Sr to join our team in a home-based role. You will monitor sites (on-site and remote), build strong investigator relationships, and collaborate with cross-functional teams to keep projects on track. Travel and a valid driver’s license are required.

The role requires a bachelor’s degree in life sciences or related field, plus at least 1 year of CRA experience. Fluency in English and Spanish is essential to support global trials.

Qualifications

• Detail-oriented and a strong problem solver.
• Highly communicative, collaborative, and adaptable.
• Motivated, accountable, and able to work independently.
• Fluent in English and Spanish; able to support virtual and in-person teams.

Responsibilities

• Monitor clinical trial sites through on-site and remote visits.
• Build and maintain strong relationships with investigators and site staff.
• Collaborate with cross-functional teams to meet project timelines.
• Manage site-level study documentation, systems updates, and visit reports.
• Implement corrective actions to maintain study integrity.
• Ensure sites are audit- and inspection-ready.

Skills

Detail-oriented

Problem solving

Strong communication

Independent worker

Team collaboration

Education

Bachelor’s degree in life sciences/related field

Job description

At Parexel, we are a leading Clinical Research Organization (CRO) specializing in delivering life‑changing medicines to patients. We are seeking an experienced Clinical Research Associate II/Sr to join our team. As a CRA, you’ll be joining a fast‑paced, driven environment that’s helping to make a life‑changing difference to patients by ensuring high‑quality clinical trial execution, building strong site partnerships, and maintaining compliance across all phases of a study. Through the collaboration and diversity of our teams, CRAs are provided with multiple opportunities to excel and discover where their skills can take them.

Who We’re Looking For

• Detail‑oriented and a strong problem solver

• Highly communicative, collaborative, and adaptable

• Motivated, accountable, and able to work independently

• Positive, professional, and comfortable supporting virtual and in‑person teams

What You’ll Do

• Monitor clinical trial sites through on‑site and remote visits

• Build and maintain strong relationships with investigators and site staff

• Collaborate with cross‑functional teams to meet project timelines

• Manage site‑level study documentation, systems updates, and visit reports

• Implement corrective actions when needed to maintain study integrity

• Ensure sites are always audit- and inspection-ready

Additional Details

• Home‑based role; preference for candidates residing in Buenos Aires

• Must be fluent in English and Spanish

• Bachelor’s degree in life sciences, pharmacy, nursing, or related field is required

• A minimum of 1 year of CRA experience required

• Must be able to travel and hold a valid driver’s license

Why Join Us

• Be part of groundbreaking projects pushing the boundaries of clinical research

• Work in a collaborative and inclusive environment that values your expertise

• Unlock career growth and professional development opportunities

• Enjoy work‑life balance and flexible working arrangements

At Parexel, we embrace flexibility and understand the importance of balancing your career with your personal life. Come join us where learning is constant and you’re exposed to a world of experiences and open doors.

#LI-REMOTE

EEO Disclaimer

Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.