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[ICD], etc.) meet regulatory requirements and company policy and has been reviewed by IRB/IECs Provides medical input into country feasibility. Support study team Has oversight of clinical input
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Consent Document [ICD], etc.) meet regulatory requirements and company policy and has been reviewed by IRB/IECs. Provides medical input into country feasibility. Support study team Provides clinical input
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[ICD], etc.) meet regulatory requirements and company policy and has been reviewed by IRB/IECs Provides medical input into country feasibility. Support study team Has oversight of clinical input
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supporting the conduct of clinical trials in the PCRU. Additional responsibilities after acquisition of relevant experience in Phase 1 clinical research activities. Represents the PCRU on company-wide