Senior Clinical Research Associate

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

Descripción de la vacante

Join a dynamic and innovative Contract Research Organization as a Clinical Research Associate. In this exciting role, you will have the opportunity to mentor and lead junior CRAs while conducting essential onsite monitoring visits. This position offers a unique chance to develop your skills and advance your career in a supportive environment. You'll be involved in study startup, site management, and collaboration with internal teams, contributing to impactful projects in the healthcare sector. If you're passionate about clinical research and ready to take the next step in your career, this role is perfect for you.

Formación

• Independent on-site monitoring experience in Mexico is essential.
• Full working proficiency in English and Spanish is required.

Responsabilidades

• Conduct and report onsite monitoring visits and manage site communication.
• Support regulatory team in preparing documents for study submissions.

Conocimientos

On-site monitoring

Communication skills

Problem-solving skills

Collaboration skills

Planning and multitasking

Educación

College/University degree in Life Sciences

Herramientas

MS Word

MS Excel

MS PowerPoint

Descripción del empleo

Company Description

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 ready to train and coordinate junior CRAs on site. Here you will have the opportunity to develop yourself as a trainer, mentor and leader. We are committed to develop our employees in their careers by providing tailored courses and mentoring.

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
• Independent on-site monitoring experience in Mexico
• Experience in all types of monitoring visits in Phase II and/or III
• Availability to travel
• Experience in Oncology or Infectious 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 tasks and 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.