PSI CRO
Healthcare
SeniorClinicalResearchAssociate
“Senior Clinical Research Associate at PSI CRO. Skills: Clinical research, Onsite monitoring, Site management. Conduct onsite monitoring visits. Report onsite monitoring visits”
Industry & Context.
Query resolution
Ability to travel up to 80%, No work visa required
What They're Looking For.
Must Have
College/University degree in Life Sciences, 5 years minimum on-site monitoring experience, Experience in all monitoring visits, Full working proficiency in English, Proficiency in MS Office applications, Valid driver’s license
Nice to Have
Experience monitoring complex Oncology trials, Experience with radiopharmaceuticals, Experience with breast cancer, Experience monitoring GI studies, Experience with IBD, Experience with Chron's, Experience with UC
What You'll Do.
Conduct onsite monitoring visits
Report onsite monitoring visits
Involved in study startup
Perform source document verification
Perform query resolution
Responsible for site communication
Responsible for site management
Supervise study activities
Supervise study timelines
Supervise study schedules
Point of contact for support
Point of contact for vendors
Involved in quality control
Participate in feasibility research
Support regulatory team
Prepare documents for submissions
How You'll Work.
Team & Collaboration
Project stakeholders; Clinical sites; Investigators; In-house support services; Vendors; Regulatory team
Process & Methodology
Study startup, Study activities, Study timelines, Study schedules
Applying for this Senior Clinical Research Associate role?
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