Join CareLyft Technologies as a detail-oriented Clinical Research Associate to support site monitoring and clinical trial oversight across multiple therapeutic areas. The ideal candidate brings hands-on experience in site management, ICH-GCP compliance, and source data verification.
CareLyft Technologies is seeking an Experienced Medical Affairs Trainer to design and deliver structured training programmes across medical communications, scientific engagement, and regulatory-aligned content development. The ideal candidate combines strong medical affairs domain expertise with a demonstrated ability to build field and cross-functional capability.
CareLyft Technologies is seeking an Experienced Medical Reviewer (MBBS) to provide clinical oversight and medical assessment across pharmacovigilance case processing, narrative writing, and safety signal evaluation. The ideal candidate brings strong medical judgement with a thorough understanding of global drug safety regulations and ICH guidelines.
CareLyft Technologies is seeking an Experienced Pharmacovigilance Trainer to design and deliver high-impact training programmes across drug safety operations and regulatory compliance. The ideal candidate brings deep PV domain knowledge with a proven ability to build capability across cross-functional teams.
We are looking for a detail-driven Product Complaint Management Data Analyst (Investigation) to oversee complaint lifecycle management, data trending, and regulatory reportability assessments for our clients' product portfolios. This role is critical in identifying safety signals, driving CAPA initiation, and ensuring compliance with global post-market surveillance requirements.