Match score not available

Senior Clinical Research Associate

extra holidays - extra parental leave
Remote: 
Full Remote
Contract: 
Experience: 
Senior (5-10 years)
Work from: 

Offer summary

Qualifications:

Degree in Life Sciences or equivalent, On-site monitoring experience in Mexico, Experience in Phase II and/or III monitoring, Fluency in English and Spanish, PC proficiency in MS Word, Excel, PowerPoint.

Key responsabilities:

  • Conduct onsite monitoring visits
  • Manage site communication and support services
  • Participate in study startup and feasibility research
  • Perform CRF review and query resolution
  • Support regulatory team for study submissions
PSI CRO AG  logo
PSI CRO AG Pharmaceuticals 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

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.

Required profile

Experience

Level of experience: Senior (5-10 years)
Industry :
Pharmaceuticals
Spoken language(s):
EnglishEnglishSpanish
Check out the description to know which languages are mandatory.

Other Skills

  • Problem Solving
  • Collaboration
  • Communication
  • Microsoft Excel
  • Microsoft PowerPoint
  • Leadership
  • Planning
  • Training And Development
  • Teamwork
  • Mentorship
  • Microsoft Word

Related jobs