EMPREGO CLINICAL TRIALS REGULATORY SUBMISSION SÃO PAULO, SÃO PAULO
(22 vagas de emprego)
Listado de trabajos de Clinical trials regulatory submission en São paulo, São paulo
• awareness of applicable clinical research regulatory requirements, i... essential functions • assist clinical research associates (cras) and regulatory and start-up...
Clinical research coordinator in sao bernardo de campo, sao paulo - part time & fixed term
As a pivotal member of the site team, you will be involved with a variety of administrative tasks to support investigators and ensure the smooth running of clinical...
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You will: interpret clinical trial protocols to create and execute an effective clinical trial supply chain solution... 2-3 years experience in clinical trial supply...
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This is an excellent opportunity if you have experience working as a nurse! as a pivotal member of the site team, you will be involved with a variety of administrative...
Sr country site activation lead in brazil
Determine regulatory strategy/expectations and parameters for submissions and all necessary authorizations... • provide specialist functional and technical scientific...
With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our ppd clinical research portfolio, our...
Pharmacovigilance manager ii - vaga exclusiva para pessoas com deficiencia (pcd)
Experienced in interacting with regulatory agencies, presenting company´s projects, defining product´s safety monitoring strategy and responding to regulatory inquiries...
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Home-based in brazil responsibilities: advise clients, project teams, sites, data safety monitoring boards, regulatory agencies and third-party vendors on medical...
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• advanced level of english • knowledge of clinical trials - knowledge of clinical trial conduct and skill in applying applicable clinical research regulatory requirements...
Crie um alerta e não perca nenhuma nova oferta do seu interesse!
Req • good knowledge of, and skill in applying, applicable clinical research regulatory requirements (i... good clinical practice (gcp) and international conference...
Fsp - (sr.) site activation specialist in brazil
• inform team members of completion of regulatory contractual... #li-nrj #li-remote iqvia is a leading global provider of clinical research services, commercial...
Req • good knowledge of, and skill in applying, applicable clinical research regulatory requirements... good clinical practice (gcp) and international conference...
Crie um alerta e não perca nenhuma nova oferta do seu interesse!
Crie um alerta e não perca nenhuma nova oferta do seu interesse!