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Clinical Research Monitor

extra holidays - extra parental leave
Remote: 
Full Remote
Contract: 
Experience: 
Mid-level (2-5 years)
Work from: 

Offer summary

Qualifications:

College/University degree in Life Sciences, Independent on-site monitoring experience in Mexico, Experience with Phase II / III monitoring visits, Full working proficiency in English and Spanish, Proficiency in MS Office applications.

Key responsabilities:

  • Conduct and report onsite monitoring visits
  • Involved in study startup and feasibility research
  • Perform CRF review, source document verification
  • Responsible for site communication and management
  • Support regulatory team in study submission documents
PSI CRO AG  logo
PSI CRO AG Large https://www.psi-cro.com/
1001 - 5000 Employees
See more PSI CRO AG offers

Job description

Company Description

PSI is a leading Contract Research Organization with more than 25 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

As a Clinical Research Associate at PSI you will enjoy a variety of monitoring tasks and work on clinical studies in different therapeutic indications, maintaining the highest quality standards in the industry. We are committed to develop our employees in their careers by providing tailored courses and mentoring. 

You will:

  • Conduct and report all types of onsite monitoring visits
  • Be involved in study startup and feasibility research
  • 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
  • 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 Mexico
  • Experience in all types of monitoring visits in Phase II / III
  • Full working proficiency in English and Spanish
  • Proficiency in MS Office applications
  • Ability to plan and work in a dynamic team environment
  • Communication, collaboration, and problem-solving skills
  • Ability to travel

Additional Information

This is a great opportunity for you to further develop your skills, widen your therapeutic area experience, and become an expert in clinical research.

Required profile

Experience

Level of experience: Mid-level (2-5 years)
Industry :
Pharmaceuticals
Spoken language(s):
EnglishEnglishSpanish
Check out the description to know which languages are mandatory.

Other Skills

  • Problem Solving
  • Collaboration
  • Communication
  • Planning
  • Teamwork

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