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Résumé du poste
A prestigious research university in New Haven seeks a Clinical Research Associate to monitor clinical trials, ensuring compliance with protocols and regulations. Responsibilities include conducting site visits, reviewing medical records, and collaborating with leadership to maintain research integrity. Candidates should possess strong communication skills, a Bachelor’s degree, and at least 5 years of clinical research experience. This full-time position allows for a hybrid working model and is crucial for conducting research ethically and effectively.
Qualifications
5 years of related clinical research experience.
GCP training required within 3 months of hire.
Master’s degree or equivalent preferred.
Responsabilités
Conduct monitoring for clinical trials for YCCI and external sites.
Review medical records for study participants.
Develop Data and Safety Monitoring Plans.
Connaissances
Advanced knowledge of monitoring techniques and practices
Understanding of clinical research processes
Professionalism and good judgment
Ability to work with confidential material
Strong written and verbal communication skills
Formation
Bachelor’s Degree in related field
SOCRA/ACRP Certification
Description du poste
A prestigious research university in New Haven seeks a Clinical Research Associate to monitor clinical trials, ensuring compliance with protocols and regulations. Responsibilities include conducting site visits, reviewing medical records, and collaborating with leadership to maintain research integrity. Candidates should possess strong communication skills, a Bachelor’s degree, and at least 5 years of clinical research experience. This full-time position allows for a hybrid working model and is crucial for conducting research ethically and effectively.
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