Participate in pre-trial procedures, archiving documents and correspondence, setting up and organizing clinical trial sites, perform on-site visits and training and mentoring of CRAs with less experience. Supporting activities to CTM regarding project management.
Número de vacantes: 1
Modalidad de trabajo: Híbrido (25%)
Tipo de contrato: Indefinido

**Requisitos**
Experience required:
- At least 4 years of monitoring experience in pharmaceutical companies or CRO.
- Perform site selection, SIV, IMV and COV in clinical studies of new and established pharmaceuticals. Experience in oncology trials is highly valued.
- Responsible for support and management of sites to ensure that projects are conducted in accordance with protocol, applicable regulation, and the latest ICH guidelines.
- Obtain, maintain and review applicable clinical documentation in a timely manner.
- Prepare and attend investigator meetings.
- Participate in hosting pertinent audits/insp...