Medical Assistant 247729

Medix™; St. Louis (MO); On-site; USD 27,552 - 38,572; Full time

Job summary

A leading staffing and recruiting organization is seeking a Clinical Research Assistant to provide vital support in clinical research. This full-time, onsite position requires Phlebotomy experience and offers opportunities for career growth. The ideal candidate will have strong organizational and communication skills and thrive in a fast-paced environment.

Qualifications

• Prior experience working with Diabetes, endocrinology, or GLP-1's preferred.
• Must be able to multi-task and re-prioritize duties as needed.
• High-energy, hands-on employee who thrives in a fast-paced work environment.

Responsibilities

• Support clinical research coordinators through direct involvement in research.
• Maintain research records and manage laboratory supplies.
• Assist with patient scheduling and monitoring visits.
• Perform routine research visits, such as vital signs and documentation.

Skills

Phlebotomy

Computer skills (Word, Excel, PowerPoint, Outlook)

Strong organizational skills

Strong communication skills

Solutions-minded attitude

Compliance-minded attitude

Ability to multi-task

Job description

4 days ago Be among the first 25 applicants

This range is provided by Medix™. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$20.00/hr - $28.00/hr

We are looking for a talented Medical Assistant or Research Assistant to join our growing team. As part of a larger national organization, we have a great local site level culture with the opportunity for tons of growth throughout your career.

This is a fully onsite role, Phlebotomy experience is required and prior experience working with Diabetes, endocrinology or GLP-1's is preferred.

Position Overview

The Clinical Research Assistant is responsible for providing support to the clinical research coordinators (CRCs) through direct and administrative involvement in the conduct of research within the clinic. It is expected that the Research Assistant would support multiple coordinators on various clinical trial protocols. The CRA is a liaison between clinic and research staff.

Responsibilities

• Work under the general supervision of the Principal Investigator (PI) on sponsored research projects performing standard research and laboratory procedures in therapeutic clinical research studies.
• Maintains research records, source documents and related equipment, lab area and supplies in a neat professional manner.
• Assists Clinical Research Coordinator(s) (CRCs) and Research Nurse(s) on study protocols by organizing regulatory files, data entry into the study specific edc, organizing source documentation in advance of a monitoring visit, obtaining dry ice when needed, unpacking and organizing lab kits, among other administrative duties.
• Handles incoming and outgoing calls for research such as: patient scheduling, pre-screening, scheduling monitoring visits.
• Performs aspects of routine research visits, such as vital signs, EKGs, medical history, and documentation.
• Must be able to multi-task and re-prioritize duties as needed.
• Computer skills are required (Word; Excel; PowerPoint; Outlook).
• Phlebotomy is required.
• Solutions-minded, compliance-minded, and results-oriented.
• Strong organizational and communication skills.
• High-energy, hands-on employee who thrives in a fast-paced work environment.

Seniority level

Not Applicable

Employment type

Full-time

Job function

Research

Industries

Staffing and Recruiting and Research Services