Clinical Research Coordinator - Goiânia - Part Time Fix Term at IQVIA

São Paulo, State of São Paulo, Brazil

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Not SpecifiedCompensation

Junior (1 to 2 years)Experience Level

Part TimeJob Type

UnknownVisa

Clinical Research, HealthcareIndustries

Requirements

Bachelor's degree in life sciences
Basic knowledge of clinical trials
Study coordinator experience
Clinically or nursing background (e.g., perform EKG, collect vital signs)
Availability to work based in Goiânia/GO
Availability to work part-time (24 hours per week)
Availability to work on a fixed term contract (6 months)

Responsibilities

Verifying and/or correcting research study information on source documents; researching queries and variances; providing feedback to the site data collector
Accurate input of trial data into the Electronic Data Capture (EDC) system and tracking visits and procedures completed against budget in the clinical trial management system (CTMS)
Preparing and maintaining study files, and timely submission of information
Collecting, submitting and assisting in maintaining relevant regulatory and ethics documents
Scheduling visits with research subjects, generating appropriate reports and documentation
Other administrative support functions such as reception, office organization and supply management

Skills

Key technologies and capabilities for this role

Clinical ResearchEKGVital SignsNursingElectronic Data Capture (EDC)CTMSRegulatory DocumentsPatient Data CollectionStudy Coordination

Questions & Answers

Common questions about this position

Is this a full-time or part-time position?

This is a part-time position requiring 24 hours per week for a fixed term of 6 months.

Where is this role based?

The role is based in Goiânia/GO and requires availability to work on-site there.

What qualifications and experience are required?

A Bachelor's degree in life sciences is required, along with basic knowledge of clinical trials, study coordinator experience, and a clinical or nursing background for tasks like performing EKG and collecting vital signs.

What are the main responsibilities of the Clinical Research Coordinator?

Responsibilities include verifying and correcting research data, inputting trial data into EDC and CTMS systems, preparing study files, collecting regulatory documents, scheduling visits, and providing administrative support.

What salary or compensation is offered for this role?

This information is not specified in the job description.

IQVIA

Advanced analytics and clinical research services

About IQVIA

IQVIA provides advanced analytics, technology solutions, and clinical research services specifically for the life sciences industry. Their services utilize extensive data resources and technology to create connections within healthcare, allowing clients to gain insights that help speed up the development and marketing of new medical treatments. This process is facilitated by their IQVIA Connected Intelligence™ system, which offers quick and flexible insights. IQVIA stands out from competitors by focusing on patient privacy, employing various technologies to protect individual data. The company's goal is to enhance healthcare outcomes by supporting biotech, pharmaceutical, and medical device companies, as well as researchers and government agencies, in understanding diseases and advancing medical science.

Durham, North CarolinaHeadquarters

1998Year Founded

$3,526MTotal Funding

POST_IPO_EQUITYCompany Stage

Cybersecurity, Biotechnology, HealthcareIndustries

10,001+Employees

Risks

Rapid advancement of cancer vaccines may disrupt traditional clinical research models.

Proliferation of disparate technological solutions causes technology overload in clinical trials.

Generative AI technologies face challenges in adoption due to data privacy concerns.

Differentiation

IQVIA leverages advanced analytics and big data for life sciences solutions.

The company offers privacy-enhancing technologies to protect individual patient data.

IQVIA's AI Assistant provides rapid, actionable insights for healthcare and life sciences.

Upsides

Increased adoption of decentralized clinical trials enhances patient-centric study designs.

AI-driven drug discovery accelerates identification of potential drug candidates.

Expansion of telemedicine facilitates remote patient monitoring and data collection.

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