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Entry Level Clinical Research Jobs in Raleigh, NC

Revival Research Institute, LLC

Phlebotomist/Lab Tech

Cary, NC · On-site

$15.75 - $19.75/hr

Additionally, 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 ...

Applied Industrial Technologies

Planner I

Raleigh, NC · On-site

$22 - $25/hr

This is an ONSITE ENTRY LEVEL position. * This job starts at $22-$25/hour. * This position is not ... PCI is proud to serve pharmaceutical, biotechnology, medical device, and clinical research ...

Genesis Global Group

Be Seen First

Entry Level Sales Executive-Raleigh/Durham, NC

Raleigh, NC · On-site

$50K/yr (+ commission)

... a CLIA certified clinical laboratory with multiple state licensing, specializing in ... Our main theme of research is in the field of Gynecology, Infectious Diseases, Infectious Arthritis ...

UNC-Chapel Hill

Business Officer 1

Chapel Hill, NC · On-site

... research. Patient care: We promote health and provide superb clinical care while maintaining our ... Minimum Education and Experience Requirements Entry-level with Masters; or Bachelors and 0-2 yrs ...

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Entry Level Clinical Research information

See Raleigh, NC salary details

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

As of Sep 8, 2026, the average hourly pay for entry level clinical research in Raleigh, NC is $22.08, according to ZipRecruiter salary data. Most workers in this role earn between $16.83 and $25.24 per hour, depending on experience, location, and employer.

What is an entry level clinical research?

An Entry Level Clinical Research job involves assisting in the planning, execution, and monitoring of clinical trials that test the safety and effectiveness of new treatments or medical devices. Responsibilities may include data collection, documentation, regulatory compliance, and supporting senior researchers. These roles are typically found in pharmaceutical companies, contract research organizations (CROs), or healthcare institutions. Strong attention to detail, organizational skills, and knowledge of Good Clinical Practice (GCP) guidelines are important for success. This position serves as a stepping stone for careers in clinical research, regulatory affairs, or healthcare innovation.

What are the typical daily responsibilities of an entry level clinical research?

In an entry level clinical research position, your day-to-day tasks may include collecting and entering study data, helping prepare regulatory documentation, monitoring study progress, and ensuring strict protocol compliance. You’ll often assist with scheduling participant visits, communicating with study subjects, and supporting senior clinical research staff. Collaboration is frequent, as you may work closely with coordinators, principal investigators, and other healthcare professionals. This hands-on experience provides a valuable foundation for understanding the research process and can open doors for career advancement in clinical research.

What are the key skills and qualifications needed for an entry level clinical research?

To thrive as an Entry Level Clinical Research professional, you generally need a bachelor’s degree in a life science or health-related field, strong attention to detail, and basic understanding of clinical trial processes. Familiarity with data entry systems, electronic data capture (EDC) platforms, and adherence to Good Clinical Practice (GCP) guidelines or certificates are often expected. Excellent organizational skills, effective communication, and a collaborative mindset help you stand out in this position. These skills ensure accurate data collection, regulatory compliance, and successful teamwork within complex research environments.

How to start a career in entry level clinical research?

To start a career in entry level clinical research, obtain a relevant bachelor's degree such as in life sciences, healthcare, or related fields. Gaining knowledge of Good Clinical Practice (GCP) guidelines, developing strong organizational skills, and seeking internships or entry-level positions can help build experience in clinical trial processes and regulatory requirements.

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

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

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

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

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

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

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

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

Entry Level Clinical Research jobs near you
Infographic showing various Entry Level Clinical Research job openings in Raleigh, NC as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $45,922 per year, or $22.1 per hour.

Clinical Research Coordinator

Revival Research Institute, LLC

Cary, NC • On-site

$22.50 - $30/hr

Full-time

Re-posted 18 days ago

Key responsibilities

  • Coordinate and manage multiple concurrent clinical studies, including site initiation, participant screening, enrollment, and study visits.

  • Collect, review, and maintain source documents, enter data into electronic data capture systems, and resolve monitoring queries.

  • Organize and ensure the completeness of trial-related regulatory documents, communicate with sponsors and IRBs, and manage investigational product accountability.

Job description

About Revival Research Institute
Revival Research Institute, LLC has been conducting industry-sponsored clinical trials since 2015. Headquartered in Metro Detroit, we operate sites across Michigan, Texas, Illinois, New Jersey, and North Carolina, and have been recognized nationally for the quality of the data we deliver to our sponsors. 
About This Role
This is not an entry-level position. We are hiring an experienced site-based coordinator who has independently run industry-sponsored interventional trials and can take ownership of assigned protocols from site initiation visit through close-out.
Clinical Research Coordinators at Revival coordinate and manage multiple concurrent studies and support the Investigators and clinical staff with study-related tasks including, but not limited to:
Responsibilities
  1. Screening, recruitment, and enrollment. Pre-screen candidates against inclusion/exclusion criteria, independently obtain informed consent on interventional protocols in accordance with ICH-GCP and 21 CFR Part 50, and conduct study visits per protocol. Collect, process, and ship research specimens, including IATA-regulated shipments, where applicable.
  2. Data and monitoring. Obtain, review, and maintain source documents contemporaneously. Enter data into EDC within sponsor-specified timelines and resolve queries within guidelines provided in the protocol. Host monitoring visits, and drive CRA findings and follow-up letters through to resolution.
  3. Regulatory and quality. Own the organization and completeness of all trial-related documents and correspondence across regulatory binders and eRegulatory systems. Implement and maintain quality control and assurance methods at the study level, and maintain inspection-ready files at all times.
  4. Sponsor and IRB communication. Serve as day-to-day point of contact for sponsors, CRAs, central labs, and IRT/IWRS vendors. Independently prepare and submit regulatory documents including amendments, continuing reviews, adverse and serious adverse event reports within required reporting windows, and protocol deviation reports.
  5. Investigational product accountability. Manage IP receipt, dispensing, reconciliation, storage conditions, and temperature excursion documentation in accordance with the protocol and sponsor requirements.
  6. Professional and technical knowledge. Maintain current working knowledge of ICH-GCP E6(R3), applicable FDA regulations, and evolving sponsor and site practices. Maintain certification and required training.
  7. Participant communication and confidentiality. Communicate with research participants and their families throughout the study lifecycle, support retention across visit schedules, and protect participant confidentiality in accordance with HIPAA.
Required Qualifications
  1. 2+ years as a Clinical Research Coordinator at a research site, serving as primary coordinator on industry-sponsored interventional trials. Academic-only, registry-only, or observational/minimal-risk experience does not meet this requirement.
  2. Demonstrated experience independently obtaining informed consent on interventional protocols.
  3. Hands-on experience with EDC platforms.
  4. Demonstrated experience hosting monitoring visits and resolving monitoring findings independently.
  5. Working knowledge of ICH-GCP E6(R3) and 21 CFR Parts 11, 50, 54, 56, and 312, and HIPAA.
  6. Current phlebotomy competency, as well as IV certification, is preferred.
  7. Proficiency in conducting physical assessments, including comfort with vital signs and 12-lead ECG acquisition.
  8. Master's degree in a health-related field, or equivalent clinical research site experience.
  9. Strong computer proficiency including Microsoft Office (Word, Excel, Outlook); excellent verbal and written communication; ability to work independently, manage competing protocol deadlines, and assume ownership of assigned studies.
  10. Ability to work on-site in Cary, NC.

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