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Job Overview

Perform a variety of administrative tasks in support of clinical trials and assist in the performance of clinical procedures to collect data on patients enrolled and/or seeking enrollment in clinical studies.

Essential Functions

• Provide clinical research support to investigators and site staff, including

• Verify and/or correct research study information on source documents; research queries and variances; and provide

feedback to the site data collector.

• Input research study data into trial Electronic Data Capture (EDC) system, maintaining quality control for content,

accuracy, and completeness.

• Prepare and maintain research study files. Compile, collate and submit study information within established deadlines.

• Collect and submit regulatory/ethics documentation pertaining to the research study.

• Maintain the FDA 1572 form for assigned research studies.

• Schedule subject visits and generate appropriate reports and documents for research subjects prior to visits.

• Input visit data into clinical trial management system (CTMS) to track patient visits and procedures completed against the study budget.

Qualifications

• High School Diploma or equivalent High School Diploma Req

• Educational equivalent and 2 years’ relevant work experience in a clinical environment or medical setting; or equivalent combination of education, training and experience Req

• Basic knowledge of clinical trials

• In-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and study

schedules

• Basic knowledge of medical terminology

• Basic skill in using MS Windows and Office applications such as Access, Outlook, Excel, and Word

• Excellent interpersonal skills

• Ability to pay close attention to detail

• Ability to establish and maintain effective working relationships with coworkers, managers and clients

• Applicable certifications and licenses as required by the company, country, state, and/or other regulatory bodies Upon Hire Req

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

• Bachelor's degree in life sciences

• Basic knowledge of clinical trials, research assistant experience

• Availability to work based in Brasilia

• Availability to work part-time (24 hours per week)

• Availability to work in a fixed term contract (6 months)

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.

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. Everything we do is part of a journey to improve patient outcomes and population health worldwide.

To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.

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