ClinChoice is a leading global full-service CRO with three decades of experience in pharmaceutical, biotechnology, medical device, and consumer health sectors. Specializing in clinical development, post-marketing and real-world evidence, quality and compliance, and technology solutions, ClinChoice offers comprehensive support worldwide with its deep regulatory expertise, robust pharmacovigilance, and project management capabilities.
ClinChoice is seeking a medical review consultant to assist in the review and verification of non-serious and serious Clinical Trial Adverse Events (ICSRs). The role involves medical review, compliance ensuring quality, and providing expert guidance to case processors. Experience in various therapeutic areas, such as Oncology, Respiratory, and Immunology, is required.
ClinChoice is a leading global full-service CRO with three decades of experience in pharmaceutical, biotechnology, medical device, and consumer health sectors. Specializing in clinical development, post-marketing and real-world evidence, quality and compliance, and technology solutions, ClinChoice offers comprehensive support worldwide with its deep regulatory expertise, robust pharmacovigilance, and project management capabilities.
Signant Health