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Company | IQVIA |
Address | Colorado, United States |
Employment type | FULL_TIME |
Salary | |
Category | Pharmaceutical Manufacturing |
Expires | 2023-09-04 |
Posted at | 9 months ago |
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
We are committed to providing equal employment opportunities for all, including veterans and candidates with disabilities. https://jobs.iqvia.com/eoe
As the COVID-19 virus continues to evolve, IQVIA’s ability to operate and provide certain services to customers and partners necessitates IQVIA and its employees meet specific requirements regarding vaccination status. https://jobs.iqvia.com/covid-19-vaccine-status
Colorado/California/Washington state Pay Transparency : The salary range for this role is $43,800 - $54,700.The actual salary will vary based on factors like candidate qualifications and competencies. Certain roles are eligible for annual bonus, sales incentives and/or stock. Benefits may include healthcare, retirement, paid time off, and more.
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
- Verify and/or correct research study information on source documents; research queries and variances; and provide
- Provide clinical research support to investigators and site staff, including
- Input research study data into trial Electronic Data Capture (EDC) system, maintaining quality control for content,
- 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.
- Prepare and maintain research study files. Compile, collate and submit study information within established deadlines.
- Basic knowledge of clinical trials
- 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
- In-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and study
- Excellent interpersonal skills
- Ability to pay close attention to detail
- Basic skill in using MS Windows and Office applications such as Access, Outlook, Excel, and Word
- Applicable certifications and licenses as required by the company, country, state, and/or other regulatory bodies Upon Hire Req
- Ability to establish and maintain effective working relationships with coworkers, managers and clients
- Basic knowledge of medical terminology
We are committed to providing equal employment opportunities for all, including veterans and candidates with disabilities. https://jobs.iqvia.com/eoe
As the COVID-19 virus continues to evolve, IQVIA’s ability to operate and provide certain services to customers and partners necessitates IQVIA and its employees meet specific requirements regarding vaccination status. https://jobs.iqvia.com/covid-19-vaccine-status
Colorado/California/Washington state Pay Transparency : The salary range for this role is $43,800 - $54,700.The actual salary will vary based on factors like candidate qualifications and competencies. Certain roles are eligible for annual bonus, sales incentives and/or stock. Benefits may include healthcare, retirement, paid time off, and more.
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