ZipRecruiter

Log In

2

Full Time Clinical Research Monitor Jobs in Raleigh, NC

Duke University

Clinical Research Coordinator

Durham, NC · On-site

$23.50 - $31.25/hr

Clinical Research Coordinator - Neurosurgery Research Be You. At Duke, we celebrate individuality ... Lead study monitoring, audit preparation, and corrective action activities. * Support study startup ...

Duke University

Clinical Research Coordinator

Durham, NC

$23.50 - $31.25/hr

Clinical Research Coordinator - Neurosurgery Research Be You. At Duke, we celebrate individuality ... Lead study monitoring, audit preparation, and corrective action activities. * Support study startup ...

Parexel

Senior Clinical Research Associate

Raleigh, NC · On-site

Hours: Full Time / 40 hours per week Summary of Duties: Engaged in monitoring clinical research that involves understanding human diseases and improving human health. Monitor and oversee clinical ...

Duke University

Clinical Research Coordinator

Durham, NC

$23.50 - $31.25/hr

As a Clinical Research Coordinator in the Ophthalmology Clinical Research Unit (CRU) , you will ... Support study monitoring visits, audits, inspections, and sponsor reviews. * Address findings and ...

Duke University

Clinical Research Coordinator

Durham, NC · On-site

$23.50 - $31.25/hr

As a Clinical Research Coordinator in the Ophthalmology Clinical Research Unit (CRU) , you will ... Support study monitoring visits, audits, inspections, and sponsor reviews. * Address findings and ...

Parexel

Senior Clinical Research Associate

Raleigh, NC · On-site +1

Hours: Full Time / 40 hours per week Summary of Duties: Engaged in monitoring clinical research that involves understanding human diseases and improving human health. Monitor and oversee clinical ...

Parexel

Senior Clinical Research Associate

Raleigh, NC · On-site

Hours: Full Time / 40 hours per week Summary of Duties: Engaged in monitoring clinical research that involves understanding human diseases and improving human health. Monitor and oversee clinical ...

Duke University

Clinical Research Coordinator

Durham, NC

$23.50 - $31.25/hr

May train others. Prepares for and provides support for study monitoring and audit visits ... Uses clinical research management system and its reports to manage research participants ...

Duke University

Clinical Research Coordinator

Durham, NC · On-site

$23.50 - $31.25/hr

May train others. Prepares for and provides support for study monitoring and audit visits ... Uses clinical research management system and its reports to manage research participants ...

Care Access

Clinical Research Coordinator I

Raleigh, NC · On-site

$23.50 - $31.25/hr

Coordinate and attend pre-study site visits, site initiation visits, and monitor visits with ... Benefits & Perks (US Full Time Employees) * Paid Time Off (PTO) and Company Paid Holidays * 100 ...

Care Access

Clinical Research Coordinator I

Raleigh, NC · On-site

$23.50 - $31.25/hr

Coordinate and attend pre-study site visits, site initiation visits, and monitor visits with ... Benefits & Perks (US Full Time Employees) * Paid Time Off (PTO) and Company Paid Holidays * 100 ...

next page

Showing results 1-20

All JobsClinical Research Monitor JobsFull Time Clinical Research Monitor JobsFull Time Clinical Research Monitor Jobs in Raleigh, NC

Full Time Clinical Research Monitor information

What are some common challenges full time clinical research monitors face when overseeing multiple clinical trial sites?

Full Time Clinical Research Monitors often encounter challenges such as coordinating communication across multiple sites, managing diverse site staff, and ensuring consistent adherence to protocols and regulatory requirements. Balancing travel, documentation, and follow-up visits can be demanding, especially when sites are geographically dispersed. Strong organizational skills, attention to detail, and effective relationship-building are crucial to ensuring trials progress smoothly and data integrity is maintained.

What are the key skills and qualifications needed to thrive as a full time clinical research monitor?

To thrive as a Full Time Clinical Research Monitor, you need a solid understanding of clinical trial protocols, Good Clinical Practice (GCP) guidelines, and a background in life sciences or nursing, often supported by a bachelor's degree. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and sometimes certification such as ACRP or SOCRA is highly valuable. Outstanding attention to detail, strong organizational skills, and effective communication are crucial soft skills for ensuring compliance and fostering collaboration among research teams. These competencies are critical for maintaining data integrity, patient safety, and regulatory compliance throughout the clinical trial process.

What is a full time clinical research monitor?

Full Time Clinical Research Monitors, also known as Clinical Research Associates (CRAs), are professionals responsible for overseeing clinical trials to ensure they are conducted according to regulatory requirements, ethical standards, and study protocols. They visit research sites to review data, verify patient records, and ensure participant safety. Their work helps confirm the accuracy and integrity of clinical trial results, playing a critical role in the development of new medical treatments and drugs.

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

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

What cities near Raleigh, NC are hiring for Full Time Clinical Research Monitor jobs?

Cities near Raleigh, NC with the most Full Time Clinical Research Monitor job openings:

Full Time Clinical Research Monitor jobs near you
Infographic showing various Full Time Clinical Research Monitor job openings in Raleigh, NC as of August 2026, with employment types broken down into 100% Full Time. Highlights an 79% In-person, and 21% Remote job distribution.

Clinical Research Coordinator

Revival Research Institute, LLC

Cary, NC • On-site

$23.75 - $31.75/hr

Full-time

Re-posted 26 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!!! 

Powered by JazzHR

cL3L2ZOIaF