ZipRecruiter

Log In

1

Day Shift Clinical Research Assistant Jobs (NOW HIRING)

Care Access

Clinical Research Assistant

Mauldin, SC

$19 - $33/hr

How This Role Makes a Difference The Clinical Research Assistant is an entry level clinical position and is designed to fully integrate the individual in the Care Access Research process while ...

Care Access

Clinical Research Assistant

Mauldin, SC · On-site

$19 - $33/hr

How This Role Makes a Difference The Clinical Research Assistant is an entry level clinical position and is designed to fully integrate the individual in the Care Access Research process while ...

Care Access

Clinical Research Assistant

Mesa, AZ · On-site

$19 - $33/hr

How This Role Makes a Difference The Clinical Research Assistant is an entry level clinical position and is designed to fully integrate the individual in the Care Access Research process while ...

Care Access

Clinical Research Assistant

Houston, TX · On-site

$19 - $33/hr

How This Role Makes a Difference The Clinical Research Assistant is an entry level clinical position and is designed to fully integrate the individual in the Care Access Research process while ...

previous pagenext page

Showing results 21-40

All JobsDay Shift Clinical Research JobsDay Shift Clinical Research Assistant Jobs

Day Shift Clinical Research Assistant information

See salary details

$11

$20

$28

How much do day shift clinical research assistant jobs pay per hour?

As of Aug 8, 2026, the average hourly pay for day shift clinical research assistant in the United States is $20.23, according to ZipRecruiter salary data. Most workers in this role earn between $16.59 and $23.32 per hour, depending on experience, location, and employer.

What is the difference between Day Shift Clinical Research Assistant vs Clinical Research Coordinator?

AspectDay Shift Clinical Research AssistantClinical Research Coordinator
ResponsibilitiesAssist with data collection, patient scheduling, and regulatory documentationOversee study operations, manage participant recruitment, and ensure compliance
CredentialsTypically requires a bachelor's degree or related certificationOften requires a bachelor's degree, with some roles preferring certification or experience
Work EnvironmentHospital or clinical setting, primarily during daytime hoursResearch sites, hospitals, or clinics, with broader responsibilities

While both roles support clinical research, the Day Shift Clinical Research Assistant focuses on assisting with data and patient tasks during daytime hours, whereas the Clinical Research Coordinator manages overall study operations and compliance. The roles often overlap in credentials and work environment but differ in scope and responsibilities.

More about Day Shift Clinical Research Assistant jobs
What cities are hiring for Day Shift Clinical Research Assistant jobs? Cities with the most Day Shift Clinical Research Assistant job openings:
What are the most commonly searched types of Day Shift Clinical Research jobs? The most popular types of Day Shift Clinical Research jobs are:
What states have the most Day Shift Clinical Research Assistant jobs? States with the most job openings for Day Shift Clinical Research Assistant jobs include:
What job categories do people searching Day Shift Clinical Research Assistant jobs look for? The top searched job categories for Day Shift Clinical Research Assistant jobs are:
Day Shift Clinical Research Assistant jobs near you
Infographic showing various Day Shift Clinical Research Assistant job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 68% Full Time, 26% Part Time, and 5% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $42,079 per year, or $20.2 per hour.

Clinical Research Assistant

ECN Operating LLC

Las Vegas, NV

Full-time

Re-posted 21 days ago

Job description

Position Summary
The Research Assistant supports the execution of clinical research studies by performing
administrative, technical, and participant-focused tasks under the supervision of the
Clinical Research Coordinator and Principal Investigator. This role plays a critical part in
ensuring high-quality data collection, regulatory compliance, and participant safety. The
Research Assistant works collaboratively with the clinical team to facilitate study activities
in accordance with Good Clinical Practice (GCP) guidelines, study protocols, and
institutional policies.


Key Responsibilities
Study Support & Coordination

  • Assist in preparing study materials, source documents, and regulatory binders.
  • Support participant screening, recruitment, and scheduling in accordance with study protocols.
  • Maintain accurate participant logs and assist in tracking enrollment progress.
  • Ensure study areas, supplies, and equipment are organized and ready for study visits.

Data & Documentation

  • Accurately record data from source documents into electronic case report forms (eCRFs) or databases.
  • Maintain confidentiality and integrity of participant data in compliance with HIPAA and institutional standards.
  • Assist in resolving data queries and ensuring timely data entry.
  • Support document management, filing, and archiving according to regulatory requirements.

Participant Interaction

  • Greet and assist study participants during visits to ensure a positive experience.
  • Prepare consent materials and provide administrative support during the informed consent process.
  • Escort participants to appropriate testing areas and assist clinical staff with noninvasive study procedures as directed.

Regulatory & Compliance

  • Follow Good Clinical Practice (GCP) and institutional policies at all times.
  • Support compliance with IRB, sponsor, and regulatory agency requirements.
  • Participate in site audits, monitoring visits, and internal quality reviews as needed.

Team Collaboration

  • Work closely with Clinical Research Coordinators, Principal Investigators, and site teams to ensure timely completion of study milestones.
  • Participate in team meetings, training, and continuing education to stay current with study and regulatory updates.
  • Contribute to process improvements and operational efficiency initiatives.

Qualifications

  • Associate or bachelor’s degree in a health sciences, biology, psychology, or related field preferred.
  • Current phlebotomy certification or previous phlebotomy experience is strongly preferred.
  • Previous experience in healthcare or research setting is strongly preferred.
  • Familiarity with clinical trials, GCP, HIPAA, and human subjects research regulations are desirable.
  • Strong organizational, communication, and time management skills.
  • Ability to work accurately in a fast-paced environment with strong attention to detail.
  • Proficiency with Microsoft Office and data entry systems; experience with EDC or CTMS systems a plus.

Core Competencies

  • Accuracy and Attention to Detail
  • Professionalism and Confidentiality
  • Team Collaboration
  • Adaptability and Initiative
  • Ethical Conduct and Compliance Awareness

Apply