Clinical Research Associate II or Senior

Parexel International; Ciudad de México; Presencial; MXN 500.000 - 700.000; Jornada completa

Descripción de la vacante

Parexel International is seeking an experienced Clinical Research Associate II/Sr to join our team. This home-based role supports oncology trials, conducting on-site and remote visits while building strong partnerships with investigators and site staff.

The ideal candidate holds a life sciences degree, 1+ year CRA experience, and is fluent in English and Spanish. Travel may be required, with preference for candidates in Mexico City, Mexico.

Formación

• Bachelor’s degree in life sciences, pharmacy, nursing, or related field.
• Minimum 1 year of CRA experience monitoring oncology trials.
• Fluent in English and Spanish.

Responsabilidades

• 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 audit- and inspection-ready

Conocimientos

Detail-oriented

Communication

Collaborative

Independent

Team player

Educación

Bachelor's degree in life sciences

Descripción del empleo

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 Mexico City
• 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 monitoring oncology trials is 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.