Clinical Trials Assistant, Real World Evidence (People with Dissabilities)

IQVIA LLC; São Paulo; Presencial; BRL 20.000 - 80.000; Tempo integral

Resumo da oferta

A leading global provider of clinical research services is seeking a Clinical Trials Assistant in São Paulo. This role involves providing project-related support, ensuring compliance with regulations, and effective coordination among project teams. Ideal candidates will have a Bachelor's in life sciences and relevant experience, contributing to innovative medical treatments and improved patient outcomes.

Qualificações

• Bachelor's Degree in life sciences preferred.
• 2 years of experience preferred.
• Basic knowledge of Microsoft Excel and Word.

Responsabilidades

• Provide project-related assistance for assigned projects and teams.
• Ensure compliance with SOPs and regulatory requirements.
• Coordinate with translation vendors and manage administrative tasks.

Conhecimentos

Communication skills

Judgment

Prioritization

Coordination

Formação académica

Bachelor's Degree in life sciences

Ferramentas

Microsoft Excel

Microsoft Word

Descrição da oferta de emprego

Clinical Trials Assistant, Real World Evidence (People with Dissabilities)

Apply locations

São Paulo, Brazil

Time type

Full time

Posted on

Posted Yesterday

Time left to apply

End Date: June 26, 2025 (30+ days left to apply)

Job requisition id

R1482856

Job Overview

Provide project-related assistance for all assigned project(s), sites, and project teams. Ensure all work is conducted in accordance with SOPs, policies, practices, good clinical practices, and applicable regulatory requirements, meeting quality and timeline metrics.

Essential Functions

1. Work on visit tracking in CTMS for Investigator payments, Vendor Setup QC’s, PV Batch Review, Passthrough invoice Batch Review & associated tasks.
2. Providing and revoking access.
3. Review ATP (Authorization to proceed) trainings.
4. Coordinating with translation vendors.
5. Understanding the contracts & enabling excellent output quality for the processing teams.
6. Ensure effective and efficient coordination between the operations team (PM/RSU/Clinical/IPA) for visit/passthrough batch query resolutions.
7. Ability to work in a deadline-oriented environment and manage SLA’s (TAT, Productivity, Quality) effectively.
8. Respond to ad-hoc requests for data/information/analysis.
9. Responsible for general administrative support for projects, tracking various activities.
10. Responsible for indexing.

Qualifications

1. Bachelor's Degree in life sciences (Preferred)
2. Life sciences graduates with typically 2 years of experience (Preferred)
3. Basic knowledge of Microsoft Excel and Word
4. Good communication skills
5. Ability to exercise judgment within procedures and practices to determine appropriate action
6. Ability to prioritize and coordinate multiple work requirements to meet deadlines
7. Ability to establish and maintain effective working relationships with co-workers, managers, and clients
8. Ability to communicate effectively with clients and project managers
9. Sitting for extended periods if work calls for it

About IQVIA

IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Our goal is to improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

About Us

IQVIA is a global leader in clinical research services, commercial insights, and healthcare intelligence. We seek diverse talent with curious minds and a commitment to innovation and impact. Everyone at IQVIA contributes to our shared goal of helping customers improve patients' lives worldwide. Thank you for your interest in growing your career with us.