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Entry Level Clinical Trial Jobs in Raleigh, NC (NOW HIRING)

Revival Research Institute, LLC

Phlebotomist/Lab Tech

Cary, NC · On-site

$15.75 - $19.75/hr

... Clinical Research field would be an excellent fit for our entry level position, with room to grow ... Maintains organization of all trial related documents and correspondence. Implement quality control ...

Revival Research Institute, LLC

Phlebotomist/Lab Tech

Cary, NC · On-site

$16.75 - $21/hr

... Clinical Research field would be an excellent fit for our entry level position, with room to grow ... Maintains organization of all trial related documents and correspondence. Implement quality control ...

All JobsClinical Trial JobsEntry Level Clinical Trial JobsEntry Level Clinical Trial Jobs in Raleigh, NC

Entry Level Clinical Trial information

See Raleigh, NC salary details

$11

$36

$66

How much do entry level clinical trial jobs pay per hour?

As of Aug 14, 2026, the average hourly pay for entry level clinical trial in Raleigh, NC is $36.62, according to ZipRecruiter salary data. Most workers in this role earn between $25.00 and $46.73 per hour, depending on experience, location, and employer.

What is an entry level clinical trial?

An Entry Level Clinical Trial job involves assisting in the planning, execution, and monitoring of clinical research studies. Responsibilities may include data entry, document management, regulatory compliance support, and coordination with clinical sites. These roles help ensure that trials follow protocols and regulatory guidelines. Typical positions include Clinical Research Coordinator, Clinical Trial Assistant, or Data Coordinator. Strong organizational skills, attention to detail, and knowledge of Good Clinical Practice (GCP) are essential for success in this field.

What does an entry level clinical trial do?

A typical day for an Entry Level Clinical Trial professional may include reviewing trial protocols, assisting with subject recruitment, collecting and entering data, and supporting study documentation efforts. You'll likely work alongside clinical research coordinators, investigators, and other team members to ensure trials are conducted according to regulatory standards. Much of the work involves meticulous record-keeping, scheduling, and frequent communication with internal and external stakeholders. The role may also involve monitoring study progress and helping resolve any logistical challenges that arise during the course of a trial. This hands-on experience provides a solid foundation for advancing into more specialized roles within clinical research.

What are the key skills and qualifications needed to thrive in an entry level clinical trial?

To thrive in an Entry Level Clinical Trial role, you need a background in life sciences or a related field, attention to detail, and knowledge of basic research methods. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and good clinical practice (GCP) guidelines is highly beneficial. Strong organization, communication, and problem-solving abilities make candidates stand out. These skills are important to ensure data accuracy, regulatory compliance, and smooth coordination within multidisciplinary research teams.

What are the most commonly searched types of Clinical Trial jobs in Raleigh, NC?

The most popular types of Clinical Trial jobs in Raleigh, NC are:

What are popular job titles related to Entry Level Clinical Trial jobs in Raleigh, NC?

For Entry Level Clinical Trial jobs in Raleigh, NC, the most frequently searched job titles are:

What job categories do people searching Entry Level Clinical Trial jobs in Raleigh, NC look for?

The top searched job categories for Entry Level Clinical Trial jobs in Raleigh, NC are:

What cities near Raleigh, NC are hiring for Entry Level Clinical Trial jobs?

Cities near Raleigh, NC with the most Entry Level Clinical Trial job openings:

Entry Level Clinical Trial jobs near you
Infographic showing various Entry Level Clinical Trial job openings in Raleigh, NC as of August 2026, with employment types broken down into 2% As Needed, 72% Full Time, 19% Part Time, and 7% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $76,160 per year, or $36.6 per hour.

Clinical Research Coordinator

Revival Research Institute, LLC

Cary, NC • On-site

$22.50 - $30/hr

Full-time

Re-posted 23 days ago

Job description

Unique opportunity to make an Impact in the healthcare industry...
Revival Research Institute, LLC was established in 2015, and headquartered in the Metro Detroit Region, and has been growing ever since. Revival now has a national presence in the Metro-Detroit Region, Texas, Illinois, and Arizona. We have been nationally acknowledged for our diligence to provide the highest quality of data for our clinical research trials.
As Revival Research Institute is growing, we are looking to add more qualified professionals to our team, who are looking for an opportunity to grow and learn with us.
We are seeking a full-time Clinical Research Coordinator with a minimum of 2 year of clinical experience, for our Woman's Health site. Someone with a strong interest in the Clinical Research field would be an excellent fit for our entry level position, with room to grow. However, this interest and background is not necessary, as our ideal candidate is an individual who is detail orientated, being able to maintain organized records, as well as someone who is motivated to learn new things, as our company is always growing and expanding into new therapeutic areas. We are looking for individuals that want the opportunity to learn and grow with us.
Clinical Research Coordinators here at Revival Research Institute, should be genuinely respectful of diverse points-of-view and strive for an environment in which inclusiveness drives productivity and results. Clinical Research Coordinators are responsible to coordinate and manage multiple studies. They are also responsible for assisting the Investigators along with other clinical staff, with any study related tasks as follows but not limited to:
  1. Participates in research participant screening, recruitment and enrollment. Consent and conduct research visits for data collection/no risk trials or no study article/minimal risk trials with oversight. Responsible for collecting, processing and shipping of research specimens, where applicable.
  2. Documents study related information in case report forms or electronic data capture systems, handles data queries and participates in monitoring visits. Obtain, review and maintain source documents.
  3. Maintains organization of all trial related documents and correspondence. Implement quality control and assurance methods.
  4. Communicate with study sponsors, research team and the Institutional Review Board. Assist with basic regulatory document preparation, with oversight e.g. study amendments, adverse event reporting, protocol deviation reporting.
  5. Maintain professional and technical knowledge about Clinical trials.
  6. Research participant/family communication, protect patient confidentiality.

Preferred Qualifications:
  1. Education/ Training: Bachelor's degree in health-related field with one to two years relevant clinical experience OR Master's degree in medical related field with no research experience. Individuals with more experience are preferred, if qualifications exceed entry level, higher positions available.
  2. Phlebotomy skills preferred.
  3. Certifications, Licensures, and Registrations: National Certification (CRA or ACRP), BLS Certification.
  4. Additional Qualifications: Expert database and computer skills: Microsoft Office (Word, Excel), Outlook, excellent verbal and written communication skills, ability to work independently and assume responsibility, excellent organizational skills, ability to meet data deadlines and maintain confidentiality. Maintain data integrity within the department. Must be able to work in a team consisting of physicians, nurses, technicians, secretarial staff and ancillary hospital staff. Knowledge of FDA Regulations and Good Clinical Practices.

IMPROVE THE FUTURE AS OUR CLINICAL RESEARCH COORDINATOR!!!

Apply