What are the responsibilities and job description for the Clinical Research Associate I position at PSI CRO?
As a Clinical Research Associate you will work on the frontline of communication with project stakeholders ensuring timelines targets and standards of clinical research projects in a variety of therapeutic indications. You will build and maintain relationships with clinical sites and investigators. You will focus on subjects rights safety and wellbeing and quality of data compliance.
HomeBased anywhere in the United States
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 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
Qualifications :
Additional Information :
Become a fullfledged 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 fullscale challenging projects.
Remote Work : Employment Type :
Fulltime
Key Skills
CSS,Cloud Computing,Health Education,Actuary,Building Electrician
Vacancy : 1
