Clinical Research Associate II

Remote: 
Full Remote
Contract: 
Work from: 

Offer summary

Qualifications:

College/University degree in Life Sciences or equivalent education and experience, At least 2 years of independent on-site monitoring experience in Portugal, Experience in Phase II and/or III monitoring visits, Full working proficiency in English and Portuguese, with MS Office proficiency..

Key responsibilities:

  • Conduct and report onsite monitoring visits including SSV, SIV, RMV, and COV
  • Perform CRF review, source document verification, and query resolution
  • Manage site communication and act as a point of contact for support services
  • Communicate study progress with internal project teams and participate in feasibility research.

PSI CRO AG  logo
PSI CRO AG Pharmaceuticals Large http://www.psi-cro.com
1001 - 5000 Employees
See all jobs

Job description

Company Description

PSI is a leading Contract Research Organization with almost 30 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 II 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.

You will:

  • Conduct and report SSV, SIV, RMV, COV onsite monitoring visits
  • 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
  • Prepare and particiapte on audits and inspections

Qualifications

 

  • College/University degree in Life Sciences or an equivalent combination of education, training & experience
  • At least 2 years of independent on-site monitoring experience in Portugal
  • Experience in all types of monitoring visits in Phase II and/or III
  • Therapeutic area experience in Oncology /Hematology /Gastroenterology (IBD) /Infectious Diseases /Neurology is a plus
  • Full working proficiency in English and Portugeese 
  • Proficiency in MS Office applications
  • Ability to plan, multitask and work in a dynamic team environment
  • Communication, collaboration, and problem-solving skills
  • Ability to travel

Additional Information

What We Offer:

  • Stability, long-term cooperation
  • Permanent contract, full-time job
  • Hybrid or home-based work setting
  • Competitive salary and benefit package
  • Career development 
  • Unique combination of team collaboration and independent work
  • Friendly and supportive colleagues
  • Onboarding courses about clinical research industry
  • Mentoring and on-the job training
  • Comfortable and well-established modern office

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

Industry :
Pharmaceuticals
Spoken language(s):
EnglishPortuguese
Check out the description to know which languages are mandatory.

Other Skills

  • Microsoft Office
  • Collaboration
  • Communication
  • Multitasking
  • Problem Solving

Research Assistant Related jobs