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unsolicited medical requests from HCPs in a manner that complies with all applicable Pfizer guidelines, policies, and procedures. Field relevant inbound queries from HCPs via established triage process. In
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unsolicited medical requests from HCPs in a manner that complies with all applicable Pfizer guidelines, policies, and procedures. Field relevant inbound queries from HCPs via established triage process. In
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s, including identification of sites serving under-represented patient populations in trials. Appropriately provide Medical support throughout the Investigator Sponsored Research (ISR) process
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s, including identification of sites serving under-represented patient populations in trials. Appropriately provide Medical support throughout the Investigator Sponsored Research (ISR) process
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s, including identification of sites serving under-represented patient populations in trials. Appropriately provide medical support throughout the Investigator Sponsored Research (ISR) process
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s, including identification of sites serving under-represented patient populations in trials. Appropriately provide medical support throughout the Investigator Sponsored Research (ISR) process
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, and procedures. Field relevant inbound queries from HCPs via established triage process In collaboration with Global Medical Affairs colleagues, partner with Worldwide Research & Development and Medical
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productive working relationships with team members. Ability to collaborate with other medical writers across therapeutic areas for template or medical writing process creation/improvement. Extensive knowledge
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quality of assigned laboratory projects in the Brussels PCRU in accordance with scientific, medical and ethical principles and with GxP requirement guidelines. Also accountable for training of data cache
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triage process. In collaboration with Global Medical Affairs colleagues, partner with Worldwide Research & Development and Medical (WRD) and Global Product Development (GPD) in the identification