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HomeCompanies9ee3716b B93b 41d4 B702 C8728d7396d2 9200736809859 2Associate Research Coordinator

Associate Research Coordinator

9ee3716b B93b 41d4 B702 C8728d7396d2 9200736809859 2 · Miami, FL, US, Miami, FL · Active · ADP Workforce Now Recruiting

Job facts

FieldValue
Company9ee3716b B93b 41d4 B702 C8728d7396d2 9200736809859 2
TitleAssociate Research Coordinator
Normalized title-
Department / team-
LocationMiami, FL, United States
Work model-
Employment typeFull Time
Salary-
Statusactive
ATS providerADP Workforce Now Recruiting
Posted / first seen2026-01-07 / 2026-05-31
Changed / last seen2026-06-06 / 2026-06-06

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PageWhat it containsOpen
Company jobsActive postings from 9ee3716b B93b 41d4 B702 C8728d7396d2 9200736809859 2.Open
Company breakdownsRole, location, ATS, and work model facets for this company.Open
ATS provider jobsActive postings observed through ADP Workforce Now Recruiting.Open
Provider filtered searchThe same provider as a filtered job collection.Open
City jobsActive postings in Miami.Open
Lifecycle eventsOpen, update, close, and reopen events for this posting.Open
Original postingCanonical source or apply URL captured from the ATS.Open

Linked records

Company9ee3716b B93b 41d4 B702 C8728d7396d2 9200736809859 2
Sourceb03b2939-16a2-4186-acef-a1c02c146929
ATS providerADP Workforce Now Recruiting

Description

Job Description Do you want to be part of an organization that is making a difference in the lives of millions of people worldwide? If so, we want to hear from you! As an Associate Research Coordinator, one will assist the research coordinator (CRC/CCRC) in conducting clinical trials. The associate research coordinator is responsible for collecting, processing, storing and handling clinical specimens (as needed), scheduling study subjects for study visits, and collecting, recording, and filing clinical research data. Additionally, the associate research coordinator conducts study visits under the supervision of a study coordinator or senior coordinator. QPS’ Story: Since its inception, QPS has been assisting pharmaceutical, biotechnology and medical device companies with their drug development efforts by providing a full range of services, including Early Phase Clinical and Phase II – IV Clinical Research services. The QPS location in Miami, Florida is a multi-specialty research center employing clinical research professionals, including board-certified physicians, in a 32,000 square foot space. To meet the needs of our clients, we strive to employ talented, caring and committed individuals who will work collaboratively towards achieving our mission of improving human health and the quality of life. Team members enjoy challenging and rewarding work and are encouraged achieve their best. Underpinning the operation is a culture that values diversity, innovation, accountability, teamwork and a friendly atmosphere where performance is recognized and rewarded. We provide unique company benefits, training, and advancement opportunities. Most importantly, we value each of our team members as employees and as individuals. If this sounds like your ideal work environment, then we would love to speak with you, so apply today! Please visit our website ( www.qps.com ) for more information and to see all current openings. The Job Ensuring GCP is followed throughout the entire study conduct. Ensuring subject confidentiality. Ensuring the subject or subject’s legal representative is provided with a copy of the signed and dated informed consent form. Possess a sound and in-depth understanding of each protocol that has been assigned Source document creation per Protocol requirements (if applicable) or as needed Ensuring compliance with applicable MRA SOP’s/MRA Clinical Research SOP’s, Good Clinical Practice guidelines and regulations Timely communication of study issues to the study coordinator Screening, Enrollment, and Ongoing Study Procedures Establish good rapport with potential study subjects Conduct telephone screening process Conduct Informed Consent Process (must complete Consenting Process module and quiz prior to consenting) Clinical data collection such as vital signs, ECG recording, subject height and weight, etc. Medical records retrieval and review Laboratory specimen collection, processing and shipment (as needed) Transporting clinical specimens to the laboratory Study visits scheduling Requirements Combination of relevant education & experience that provides sufficient knowledge & skills to ensure incumbent’s success in this role, such as: High School Diploma, and/or Experience in a similar role Prior experience as a medical assistant or in an ancillary or allied health specialty a plus Must be flexible to work evenings, weekends, and holidays as needed. Why You Should Apply Great learning opportunities, especially for those new to the field. Our seasoned professionals are here to support and work with you to explore your learning potential and career goals. Bonuses and merit increases are a part of the QPS total rewards approach and are linked to individual, team and company performance. Solid Benefits package, including Company-matched 401(k), and Company-sponsored Group Life/AD&D and Short and Long-term Disability Insurance QPS is an Equal Employment Opportunity/Affirmative Action Employer. In accordance with federal, state, and local laws, we recruit, hire, promote and evaluate all personnel without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, citizenship status, physical disability, protected veteran status, or any other characteristic protected by law. Job applicants and present employees are evaluated solely on ability, experience, and the requirements of the job. In addition, QPS, LLC is a federal contractor and desires priority referrals of protected veterans.

Full job record

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Source IDb03b2939-16a2-4186-acef-a1c02c146929
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Provider Job Key585366
TitleAssociate Research Coordinator
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Statusactive
Activeyes
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CountryUnited States
RegionFL
CityMiami
Salary Raw
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First Seen At2026-05-31 18:49:35Z
Last Seen At2026-06-06 11:49:48Z
Last Checked At2026-06-06 11:49:48Z
Last Changed At2026-06-06 11:49:48Z
Inactive At
Source Posted At2026-01-07 17:44:00Z
Source Updated At
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    "requisitionDescription": "<div><p data-pasted=\"true\"><strong>Job Description</strong></p><p><strong>Do you want to be part of an organization that is making a difference in the lives of millions of people worldwide? If so, we want to hear from you!&nbsp;</strong> As an Associate Research Coordinator, one will assist the research coordinator (CRC/CCRC) in conducting clinical trials. The associate research coordinator is responsible for collecting, processing, storing and handling clinical specimens (as needed), scheduling study subjects for study visits, and collecting, recording, and filing clinical research data. &nbsp; Additionally, the associate research coordinator conducts study visits under the supervision of a study coordinator or senior coordinator.</p><p><strong>QPS&rsquo; Story:</strong></p><p>Since its inception, QPS has been assisting pharmaceutical, biotechnology and medical device companies with their drug development efforts by providing a full range of services, including Early Phase Clinical and Phase II &ndash; IV Clinical Research services. The QPS location in Miami, Florida is a multi-specialty research center employing clinical research professionals, including board-certified physicians, in a 32,000 square foot space. 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