Clinical Research Coordinator Apprentice
Job in
Little Rock, Pulaski County, Arkansas, 72208, USA
Listing for:
Apprenticely
Apprenticeship/Internship
position
Listed on 2026-01-15
Job specializations:
-
Healthcare
Clinical Research
Salary/Wage Range or Industry Benchmark: 20 USD Hourly
USD
20.00
HOUR
Job Description & How to Apply Below
Apprenticely is helping CARTI hire a Clinical Research Coordinator Apprentice in Little Rock, AR.
About the Employer
Welcome to CARTI, where compassionate care meets leading‑edge treatment. Since 1976, CARTI has been at the forefront of cancer care, offering comprehensive services for adult cancer, blood disorders and related issues. Our expert team provides a full spectrum of treatment options, including surgery, chemotherapy and radiation therapy, alongside specialized urologic care and diagnostic radiology.
At CARTI, our mission
Amazon to make trusted cancer care accessible to every patient we serve through compassionahami, innovation and purpose. We are an independent, not‑for‑profit provider, treating over 60,000 patients annually from every county in Arkansas and beyond.
$20 – $20 an hour
Job Summary We are seeking a motivated and enthusiastic Intern to join our dynamic Clinical Research team. This apprenticeship will provide hands‑on experience in various Clinical Research functions, including screening subjects, recruiting subjects, research visits, study activities, and administrative support. The ideal candidate is eager to learn, detail‑oriented, and passionate about building a career in Clinical Research.
Job Duties and Responsibilities Didactics
Attend all didactic sessions and actively participate in discussions.Complete monthly assessments and obtain '..'.Take the final exam and achieve a passing-As excel covers demonstration.Hands‑On Training
Participate in patient screening, informed consent discussions, participant assessments, scheduling of procedures, and retention efforts. Notify the research team of relevant study activities.Complete case report forms (CRFs) accurately and respond to sponsor queries in a timely manner.Participate in subject visits and ensure that all subject questionnaires are complete, legible, and accurate, in accordance with ALCOA principles (Attributable, Legible, Contemporaneous, Original, and Accurate).Conduct follow‑up communications with study subjects regarding study objectives and document all interactions appropriately.Maintain complete and accurate study records, and file documents in accordance with protocol and system requirements.Understand and comply with regulatory guidelines and institutional policies relevant to each study and associated regulatory agencies.Assist in managing study supplies, including documentation of receipt, tracking expiration dates, and reviewing sponsor‑provided study manuals.Update team tracking reports regularly, provide database‑generated reports when requested, and support the execution of project tasks as assigned.Participate in the collection, processing, labeling, storage, and shipment of specimens vostri following protocol‑specific requirements.Prepare descriptive reports summarizing research study progress and outcomes, utilizing appropriate study systems and data records.Attend meetings with team members, investigators, and sponsors as required.Maintain a high level of organization, attention to detail, and efficiency in a fast‑paced research environment.Keep training records current and ensure compliance with all required study trainings.Education, Certification, Licensure, Registration
Bachelor’s degree in a scientific discipline or related field.IATA Certificate – required within 30 days of hire.ICH GCP Certificate – required within 30 days of hire.CITI Training – required within 30 days of hire.Experience, Knowledge, Skills, and Abilities
Must have excellent computer skills.Excellent written and verbal communication skills.Ability to(prev) work as part of a community.Medical Terminology knowledge.Analytical mindset to collect and interpret data.Outstanding organizational skills.Ability to work independently.Proficiency in data management.Strong time management skills.Reasoning Ability
Ability to solve practical problems and deal with a variety of concrete variables in situations where only limited standardization exists.Ability to interpret a variety of instructions furnished in written, oral, or schedule form.Interpersonal Skills
Must interact and communicate both verbally and in written form.Must interact…
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