Full-Time Senior Clinical Research Associate

We are seeking an experienced Clinical Research Associate to train and supervise junior CRAs on-site. This role offers opportunities for professional growth as a trainer, mentor, and leader.

We are committed to employee development and offer tailored courses and mentorship programs.

Only English CVs will be considered.

Home-based position in Mexico.

Your responsibilities will include:

• Conducting and reporting all types of on-site monitoring visits.
• Participating in study startup (if applicable).
• Performing CRF review, source document verification, and query resolution.
• Managing site communication and relationships.
• Serving as a point of contact for in-house support services and vendors.
• Communicating with internal project teams about study progress.
• Participating in feasibility research.
• Supporting the regulatory team in preparing study submission documents.

Qualifications:

• College/University degree in Life Sciences or equivalent.
• Independent on-site monitoring experience in Mexico.
• Experience with all types of monitoring visits in Phase II and/or IIIA.
• Availability to travel.
• Experience in Oncology or Infectious Diseases is a plus.
• Full working proficiency in English and Spanish.
• Proficient in MS Word, Excel, and PowerPoint.
• Strong planning, organizational, and problem-solving skills.
• Excellent communication and collaboration skills.

Join a supportive and knowledgeable team and develop a diverse skill set while working on challenging projects.

What is the last date for applying to the job?

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