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Senior Clinical Research Associate (Contractor)

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

Offer summary

Qualifications:

College/University degree in Life Sciences or equivalent, Independent on-site monitoring experience in Peru, Experience in Phase II and III monitoring visits, Full working proficiency in English and Spanish, PC skills for MS Word, Excel, PowerPoint.

Key responsabilities:

  • Conduct and report onsite monitoring visits
  • Be involved in study startup if applicable
  • Perform CRF review and source document verification
  • Manage site communication and liaison with services
  • Support regulatory team in submission preparation
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

We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 2,500 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.

    Job Description

    We are looking for a temporary freelancer Clinical Research Associate to work on the frontline of communication with project stakeholders, ensuring timelines, targets and standards of clinical research projects in a variety of therapeutic indications. 

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

    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 Peru
    • Experience in all types of monitoring visits in Phase II and/or III
    • Availability to travel
    • 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
    • Planning
    • Teamwork
    • Microsoft Word

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