Senior Clinical Research Associate

Psicro; Ciudad de México; A distancia; MXN 200,000 - 400,000; Jornada completa

Descripción de la vacante

A leading Contract Research Organization is seeking an experienced CRA II to advance to a Senior CRA position. This role offers the chance to develop as a trainer and mentor while conducting onsite monitoring visits and managing site communication. Candidates should have a degree in Life Sciences and 3-4 years of independent monitoring experience, with proficiency in English and Spanish.

Formación

• 3 - 4 years of independent on-site monitoring experience in Mexico.
• Experience in all types of monitoring visits in Phase II and/or III.

Responsabilidades

• Conduct and report all types of onsite monitoring visits.
• Be responsible for site communication and management.
• Support regulatory team in preparing documents for study submissions.

Conocimientos

Communication

Collaboration

Problem Solving

Educación

College/University degree in Life Sciences

Herramientas

MS Word

Excel

PowerPoint

Descripción del empleo

PSI is a leading Contract Research Organization with more than 27 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications.

Job Description

We are looking for an experienced CRA II ready to take next step and become a Senior CRA. Here you will have the opportunity to develop yourself as a trainer, mentor and leader!

Only CVs in English will be considered
Home-based position in Mexico

You will:

• Conduct and report all types of onsite monitoring visits
• Be involved in study startup (if applicable)
• Perform CRF review, source document verification and query resolution
• Be responsible for site communication and management
• Be a point of contact for in-house support services and vendors
• Communicate with internal project teams regarding study progress
• Participate in feasibility research
• Support regulatory team in preparing documents for study submissions

Qualifications

• College/University degree in Life Sciences or an equivalent combination of education, training & experience
• 3 - 4 years of independent on-site monitoring experience in Mexico
• Experience in all types of monitoring visits in Phase II and/or III
• Availability to travel
• Experience inOncology orInfectious Diseases is a plus
• Full working proficiency in English and Spanish
• PC skills to be able to work with MS Word, Excel and PowerPoint
• Ability to plan, deal with different tasksand work in a dynamic team environment
• Communication, collaboration, and problem-solving skills

Additional Information

Become a full-fledged clinical research professional with the support of a knowledgeable and professional team.You will develop a variety of skills while progressing with the company and contributing to our full-scale challenging projects.