Analista PCP
Core
Facilitates and coordinates the execution of contracted clinical and laboratory studies (in vitro, in vivo, P&D) for life sciences clients, ensuring timely delivery and billing.
Role type
Project Coordinator / Study Administrator
Builds
Clinical trials, bioequivalence studies, quality control studies, and P&D projects
Domain
Life Sciences / Clinical Research / Pharmaceutical Testing
Deliverable
client delivery
Required skills
Project structuring, billing administration, document management, regulatory compliance tracking, client communication, system administration
Preferred skills
Intermediate Excel, negotiation, team collaboration
Technologies
Microsiga, Office Suite
Responsibilities
Create and structure study projects (in vitro, in vivo, P&D) within the system; Manage billing tasks and contract updates; Digitize and organize study documents; Track regulatory requirements (ANVISA) and coordinate responses; Coordinate study scheduling and material acquisition; Monitor study progress and communicate status to clients; Prepare internal procedures.
Seniority
Individual Contributor