Clinical Research Associate II
Clinical Research Associate II
Posted on :
15-01-2025
Employer Active
1 Vacancy
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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.
You will:
- Conduct and report 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 inhouse 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 participate on audits and inspections
Qualifications :
- College/University Life Sciences Degree and a Masters Degree in Clinical Trials is required.
- At least 1 year of independent onsite monitoring experience in Spain
- Experience in all types of monitoring visits in Phase II and/or III
- Full working proficiency in English Spanish and Catalan
- Proficiency in MS Office applications
- Ability to plan multitask and work in a dynamic team environment
- Communication collaboration and problemsolving skills
- Ability to travel
Additional Information :
What We Offer:
- Stability longterm cooperation
- Permanent contract fulltime job
- 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
- Comfortable and well established 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.
Remote Work :
No
Employment Type :
Fulltime
Employment Type
Full-time
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