1

Clinical Research Medical Assistant Jobs (NOW HIRING)

Medical Assistant

Mount Pleasant, SC

$17 - $21.75/hr

Who We Are DelRicht is a clinical research company dedicated to providing an excellent customer ... Medical Assistant's Main Objective Overall, the Clinical Research Coordinator is responsible for ...

Clinical Research Assistant

Dallas, TX · On-site

$19.23 - $23.08/hr

The Clinical Research Assistant (RA) provides foundational support in the conduct of clinical ... Obtain, track, and manage medical releases, as well as medical and pharmacy records from external ...

The Clinical Research Assistant (RA) provides foundational support in the conduct of clinical ... Obtain, track, and manage medical releases, as well as medical and pharmacy records from external ...

Showing results 41-60

Clinical Research Medical Assistant information

See salary details

$12

$20

$27

How much do clinical research medical assistant jobs pay per hour?

As of Aug 9, 2026, the average hourly pay for clinical research medical assistant in the United States is $20.45, according to ZipRecruiter salary data. Most workers in this role earn between $17.31 and $22.12 per hour, depending on experience, location, and employer.

What is the difference between Clinical Research Medical Assistant vs Clinical Research Coordinator?

AspectClinical Research Medical AssistantClinical Research Coordinator
CertificationsCPR, Medical Assistant CertificationRelevant research certifications, sometimes medical background
Work EnvironmentClinics, research sites, hospitalsResearch sites, hospitals, academic institutions
Job ResponsibilitiesAssisting with patient procedures, data collection, preparing research areasManaging study protocols, recruiting participants, data management

The Clinical Research Medical Assistant and Clinical Research Coordinator roles share some certifications and work environments but differ mainly in responsibilities. Medical Assistants focus on supporting clinical procedures, while Coordinators oversee entire research studies. Both roles are essential in clinical research settings, with the Medical Assistant often serving as a support staff member.

What does a clinical research medical assistant do?

A clinical research medical assistant supports clinical trials by preparing study sites, scheduling patient visits, collecting and recording data, and assisting with patient care under the supervision of research coordinators and healthcare professionals. They often handle administrative tasks, ensure compliance with protocols, and may use electronic health records and research management tools. Certification and knowledge of Good Clinical Practice (GCP) are beneficial for this role.

What skills and qualifications are needed to be a clinical research medical assistant?

To thrive as a Clinical Research Medical Assistant, you need a solid background in patient care, medical terminology, and knowledge of clinical research protocols, often supported by a medical assistant certification. Familiarity with electronic data capture systems, EHRs, and Good Clinical Practice (GCP) guidelines is typically required. Attention to detail, organizational skills, and effective communication help you excel in managing study documentation and patient interactions. These skills ensure accurate data collection, regulatory compliance, and smooth coordination within clinical research teams.

What is a clinical research medical assistant?

Clinical Research Medical Assistants are healthcare professionals who support clinical research studies by assisting with patient care, collecting data, maintaining study documentation, and ensuring protocols are followed. They work closely with research coordinators, nurses, and physicians to facilitate the smooth operation of clinical trials. Their responsibilities may include scheduling appointments, drawing blood, recording vital signs, and handling research specimens. This role is essential for ensuring that research studies are conducted safely, ethically, and in compliance with regulations.

What unique challenges do clinical research medical assistants face when balancing patient care and research protocols?

Clinical Research Medical Assistants often encounter the challenge of balancing compassionate patient care with strict adherence to research protocols and regulatory requirements. They must ensure detailed and accurate data collection while maintaining patient comfort and confidentiality. Additionally, they collaborate closely with research coordinators, physicians, and laboratory staff, which requires strong communication skills and adaptability. Staying organized and up-to-date with frequently changing study guidelines is essential for success in this role.
More about Clinical Research Medical Assistant jobs
What cities are hiring for Clinical Research Medical Assistant jobs? Cities with the most Clinical Research Medical Assistant job openings:
What states have the most Clinical Research Medical Assistant jobs? States with the most job openings for Clinical Research Medical Assistant jobs include:
Infographic showing various Clinical Research Medical Assistant job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, and 6% Contract. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution, with an average salary of $42,540 per year, or $20.5 per hour.

Clinical Research Assistant

Velocity Clinical Research, Inc.

Grand Island, NE • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 4 days ago


Velocity Clinical Research rating

7.3

Company rating: 7.3 out of 10

Based on 5 frontline employees who took The Breakroom Quiz

77th of 120 rated laboratories


Job description

Velocity Clinical Research is an owned and integrated research site organization, providing excellence in patient care, high quality data and fully integrated research sites. At Velocity, we align our values and behaviors to give our employees the best chance of delivering on our brand promise: to bring innovative medical treatments to patients. We are committed to making clinical trials succeed by generating high quality data from as many patients as possible, as quickly as possible while providing exemplary patient care at every step.

As an employee of Velocity, you are the most integral part of our mission. For talented candidates who perform at a high level, Velocity will invest to support career advancement and reward performance. Whether you are new to clinical research or are an industry veteran, we invite you to apply to Velocity.

Benefits include medical, dental and vision insurance, paid time off and company holidays, 401(k) retirement plan with company-match, and an annual incentive program.

Summary:

The Clinical Research Assistant assists the Clinical Operations Team in a multi-functional capacity to carry out all assigned tasks associated with the collection, documentation, and maintenance of clinical data including phlebotomy/laboratory, data entry and administrative responsibilities.


Duties/Responsibilities:

  • Assist in the conduct of clinical trials in accordance with the study protocol, GCP, ICH Guidelines, and Velocity’s SOPs
  • Perform venipuncture, capillary puncture and/or other fluid collection within scope of the protocol and local law and regulations
  • With supervision, perform clinical assessments (vital signs, phlebotomy, ECG, etc) within scope of the protocol, local law and regulations
  • Process, package and ship laboratory specimens as required per protocol and IATA regulations, if applicable
  • Track, order and maintain inventory of all laboratory and study related supplies throughout course of the clinical trial
  • Enter source data into the sponsor's and/or vendor’s data portal and resolve basic queries in a timely manner under the direction of the Clinical Research Coordinator
  • Communicate with coworkers, leadership, study subjects, sponsors, CROs, and vendors under the direction of the Clinical Research Team
  • Understand good documentation practices when collecting, transferring data to sponsor/CRO data capture systems and resolving queries under the direction of the Clinical Research Coordinator
  • Understand the informed consent process with emphasis on ensuring initial and ongoing consent of study subjects
  • Understand basic elements of regulatory documentation required to initiate, maintain and close a clinical research trial
  • Understand and participate in patient recruiting tasks including but not limited to prescreening potential subjects for clinical research trials either via phone or in person
  • Maintain confidentiality of patient protected health information, sponsor confidential information and Velocity confidential information
  • Ability to escalate potential patient safety issues such as adverse events, serious adverse events, and adverse events of special interest to the Clinical Research Team
  • Cleaning, organizing, and disinfecting the patient care, lab and lab equipment areas as needed
  • Prepare source document charts, copy and/or file medical records and study related documents as required.
  • Perform front office duties as needed including but not limited to answering phones, scheduling subjects, making reminder calls and updating patient tracking systems.
  • Other duties as assigned

Education/Experience:

  • High School Graduate and/or technical degree with minimum of 1 year of relevant experience in life sciences industry

Required Licenses/Certifications:

  • Phlebotomy if applicable and required by state law
  • Intramuscular dose administration and preparation if applicable and required by state law

Required Skills:

  • Demonstrated knowledge of medical terminology
  • Demonstrated ability to use the following technology: Computers, Microsoft Office software, fax, copier, and multi-line telephone.
  • Understanding of verbal, written, and organizational skills
  • Demonstrated ability to work as a team player
  • Demonstrated ability to read, write, and speak English
  • Demonstrated ability to multi-task
  • Demonstrated ability to follow written guidelines
  • Demonstrated ability to be flexible/adapt as daily schedule may change rapidly

Required Physical Abilities:

  • Sit or stand for long periods of time
  • Communicate in person and by a telephone
  • Limited walking required
  • Limited to lifting up to 30 pounds

NOTE: The above Job Description is intended to communicate the general function of the mentioned position and by no means should be considered an exhaustive or complete outline of the specific tasks and functions that will be required.  Additionally, specific tasks and duties of the position are subject to change as the Company, the department and circumstances change.  All employees are expected to perform their duties within their ability as required by the job and/or as requested by management.



What Velocity Clinical Research employees say

Hours and flexibility

Workplace

Get the full story on Breakroom