If you are currently a CRA I looking forward to the next step of your career this might be the right position for you!
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 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
- 1 - 2 years of independent on-site monitoring experience in Argentina
- 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.
Remote Work :
No
Employment Type :
Full-time
If you are currently a CRA I looking forward to the next step of your career this might be the right position for you!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...
If you are currently a CRA I looking forward to the next step of your career this might be the right position for you!
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 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
- 1 - 2 years of independent on-site monitoring experience in Argentina
- 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.
Remote Work :
No
Employment Type :
Full-time
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