Psicòleg/A Juvenil Per Programa D'Escolta Jove

Doble Via Cooperativa; Barcelona; A distancia; EUR 55.000 - 70.000; Jornada completa

Descripción de la vacante

IQVIA is seeking a Clinical Monitoring Analyst (CMA) for a remote role with responsibilities around Centralized Monitoring. You will set up, program, and refresh the CMA platform according to the Centralized Monitoring Plan (CMP) and act as a lead resource within the monitoring team.

The position emphasizes independent work and cross-functional collaboration across sponsor projects. The role requires 3–5 years in clinical data management or data analysis in regulated environments and SAS

Formación

• 3–5 years of experience in clinical data management and/or data analysis in a regulated environment.
• SAS programming skills are required.
• Ability to act independently and lead monitoring team resources.
• Experience with centralized monitoring processes and CMP concepts.

Responsabilidades

• Set up, program, and refresh the Centralized Monitoring platform according to the study CMP.
• Lead and coordinate the monitoring team and collaborate with cross-functional teams.
• Manage client communications and deliverables for the sponsor project.

Conocimientos

SAS programming

Descripción del empleo

Clinical Monitoring Analyst (Cluepoints) - Remote

London, United Kingdom
Budapest, Hungary
Reading, Berkshire, United Kingdom
Bloemfontein, South Africa
Dublin, Ireland
Centurion, South Africa
Barcelona, Spain
Sofia, Bulgaria
Madrid, Spain
Full time
R This unique role within IQVIA lends itself to a Lead programmer on Cluepoints called Centralized Monitoring Analyst (CMA) with strong communication and organisation skills. Having experience with SAS programming is necessary.
This role is part of a sponsor dedicated project where you will be working with the client directly to manage deliveries.
The CMA contributes to the execution of the Centralized Monitoring process by performing the setup, programming and refresh(es) of the Centralized Monitoring platform, according to the study‑specific Centralized Monitoring Plan (CMP).
Basic expectation of the CMA is to act independently, act as a lead resource within the monitoring team, collaborate with cross‐functional teams and acquire a broad knowledge of the study content and deliverables.
Qualifications: 3‑5 years of experience in clinical data management and/or data analysis within a regulated environment. SAS skills required. CMA should be able to
Current best practice and tools – data quality, Key Risk Indicators (KRI) terminology – global study plan, integration and compliance reviews – comprehensive and simple methodology; belong at a review, identify, analyze, and diagnose of protocol changes.