Clinical Research Coordinator - Fortaleza-- Part Time Fix Term

IQVIA; São Paulo; Presencial; BRL 39 000 - 61 000; Tempo parcial

Resumo da oferta

IQVIA in Fortaleza, Brazil is seeking a Clinical Research Coordinator to support a busy site in a 24-hour-per-week role for six months. The position offers hands-on experience in clinical trials and direct collaboration with investigators.

You will assist with protocol reviews, participant recruitment, data collection and regulatory documentation, perform routine study procedures, and help coordinate site operations, training, and study timelines.

Qualificações

• Bachelor's degree in life sciences.
• Basic knowledge of clinical trials and study coordination.
• Availability to work in Fortaleza, Ceará.
• Part-time availability (24 hours/week) for 6 months.
• Recruitment experience is desirable.

Responsabilidades

• Provide operational support to investigators, review protocols and CRF understanding, EDC navigation.
• Manage study participants: recruitment, screening, informed consent, visits.
• Ensure regulatory documentation and QC, ethics submissions.
• Execute clinical procedures as needed (ECG, sample collection, vitals).
• Coordinate site operations: lab logistics, monitoring visits, audits and training.
• Assist with budgeting, timelines, and staffing needs.

Conhecimentos

Availability to work in Fortaleza

Recruitment experience

Study coordinator experience

Basic knowledge of clinical trials

Formação académica

Bachelor's degree in life sciences

Descrição da oferta de emprego

Are you looking for an opportunity in Clinical Research? Do you want to work for an industry leading company that offers you experience and supports career progression whilst giving you the option of working flexibly? If so, come and join us - IQVIA are looking Clinical Research Coordinator.

This role has an immediate start working 24 hours a week for a period of 6 months to support the site. The study coordinator should have experience clinically .

This is an excellent opportunity if you have experience working as a SC

As a pivotal member of the site team, you will be involved with a variety of administrative tasks to support investigators and ensure the smooth running of clinical trials and assist with collecting patient data.

Day to day responsibilities will include:

• Provide full operational support to investigators, including protocol review, CRF understanding, EDC navigation and participation in study meetings.
• Manage study participants, handling recruitment, screening, informed consent, visit scheduling, study procedures and ongoing subject communication.
• Ensure regulatory and documentation compliance, preparing ethics submissions, maintaining source documents, entering data, performing QC and resolving queries.
• Execute clinical procedures, such as ECG, sample collection, spirometry, vital signs, dose verification, cannulation and telemetry monitoring.
• Coordinate site operations, including lab logistics, safety reporting, preparation for monitoring visits, audits, inspections and training of new staff.
• Support study oversight, contributing to budget/timeline adherence, maintaining training records and assisting with staffing and scheduling needs.

We are looking for candidates with the following skills and experience:

• Bachelor's degree in life sciences
• Basic knowledge of clinical trials, study coordinator experience
• Availability to work based in Fortaleza, Ceará
• Availability to work part-time (24 hours per week)
• Availability to work in a fixed term contract (6 months)
• Experience with Recruitment activities is desired.

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

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.