PSI CRO
pharmaceutical
ClinicalResearchAssociateII
“Clinical Research Associate II at PSI CRO. Skills: Clinical monitoring, Site management, Regulatory support. Conduct onsite monitoring visits. Report onsite monitoring visits”
Industry & Context.
Query resolution
Ability to travel, Valid driver’s license
What They're Looking For.
Must Have
College/University degree in Life Sciences, 2 years independent on-site monitoring experience in Portugal, Full working proficiency in Portuguese, Full working proficiency in English, Full working proficiency in MS Office applications, Ability to plan, Ability to multitask, Ability to work in a dynamic team environment, Ability to travel, Valid driver’s license
Nice to Have
Experience in Oncology, Experience in Hematology
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
Point of contact for support services
Point of contact for vendors
Communicate with project teams
Involved in site identification process
Support regulatory team
Prepare documents for study submissions
Participate in audits
Prepare for inspections
Participate in inspections
How You'll Work.
Team & Collaboration
Internal project teams; Support services; Vendors
Applying for this Clinical Research Associate II role?
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ANONYMOUS · UNFILTERED
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