PSI CRO ยท 10 hours ago
Senior Clinical Research Associate
PSI CRO is a dynamic, global company focused on medical science and improving lives through new medicines. As a Senior Clinical Research Associate, you will ensure the successful execution of clinical research projects by managing timelines, building relationships with clinical sites, and ensuring compliance with safety and quality standards.
Business Information SystemsHealth CarePharmaceutical
Responsibilities
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
Supervise study activities, timelines, and schedules on the country level
Be a point of contact for in-house support services and vendors
Be involved in quality control, such as compliance monitoring and reports review
Participate in feasibility research
Support regulatory team in preparing documents for study submissions
Qualification
Required
College/University degree in Life Sciences or an equivalent combination of education, training & experience
Independent on-site monitoring experience in the USA (5 years minimum)
Experience in all types of monitoring visits in Phase I-III
Participation in clinical projects as a Senior Monitor
Experience monitoring complex Oncology trials required
Full working proficiency in English
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 up to 80%
Valid driver's license (if applicable)
Preferred
Experience with radiopharmaceuticals and/or breast cancer
Experience monitoring GI studies (IBD, Chron's, UC)
Company
PSI CRO
PSI is a leading full-service global Contract Research Organization whose key strength is predictable patient enrollment across multiple therapeutic areas.
Funding
Current Stage
Late StageRecent News
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