Lead Regulatory Compliance Specialist

Job Title: Process Control Compliance ManagerJob SummaryAs a key member of the team, you will be responsible for ensuring compliance with process standards by overseeing audit and inspection readiness, participating in client and regulatory audits, and implementing corrective actions as needed.

The Clinical Team Lead (CTL) is the leader for the clinical team in our Clinical Operations **CTL** group. The Clinical Team Lead (CTL) is responsible and accountable for the execution of the clinical operations component of the project, at the global or regional level, as assigned. The CTL is responsible for working cross functionally, within a matrix...

Manage the receipt and processing of all adverse event reports reported either spontaneously from any source or from a clinical trial. This includes, but is not limited to: - entry of safety data onto adverse event database(s) and tracking systems - review of adverse events for completeness, accuracy and appropriateness for expedited reporting - write...

Clinical Research Associate JobAre you a detail-oriented and organized professional seeking a challenging role in clinical research? Do you have excellent communication and problem-solving skills? We are looking for a Clinical Research Associate to join our team!The successful candidate will be responsible for monitoring and managing clinical trial sites,...

**Main activities** - Oversee audit/inspection readiness and participate in audits from client and inspections from regulatory authorities. - Liaise with QA and regulatory in development of CAPA actions for CQIs and audit/inspection findings - Contribute and oversee implementation of CAPA actions as per the timelines - Ensure PSS teams’ compliance to...

**Main activities** - Ensures Labcorp systems accuracy, reflecting site readiness to enroll. - Ensures clinical sites are ready for the first day that the drug trial begins. The jobholder performs the above with some supervision. - Maintains allocated site’s information and associated regulatory documents throughout the duration of the clinical trial. -...

Labcorp Drug Development is a leading global drug development services company and we provide support to the Pharmaceutical and Biotechnology industries. Are you ready for the next step in your career? We are currently recruiting for a Clinical Research Associate II in Brazil. Role description: - Ensure the study staff who will conduct the protocol have...

Job Title: Clinical Research Associate II RoleThis role is responsible for site monitoring, data management and regulatory compliance. The ideal candidate will have a strong background in clinical research, excellent communication skills and the ability to work independently.Responsibilities:- Conduct site initiation and routine visits to ensure study...

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...

Nos encontramos en la búsqueda de un/a AML/KYC Compliance Team Lead.¿Cuáles serán tus funciones?- Coordinar, asignar y monitorear la carga de trabajo del equipo, garantizando la productividad y el cumplimiento de estándares.- Guiar al equipo en procesos de evaluación de riesgo, validación de clientes y screening de AML/sanciones.- Actuar como...