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Clinical trials specialist vs research coordinator

The differences between clinical trials specialists and research coordinators can be seen in a few details. Each job has different responsibilities and duties. It typically takes 1-2 years to become both a clinical trials specialist and a research coordinator. Additionally, a clinical trials specialist has an average salary of $74,910, which is higher than the $48,974 average annual salary of a research coordinator.

The top three skills for a clinical trials specialist include patients, clinical research and clinical trials. The most important skills for a research coordinator are patients, informed consent, and data collection.

Clinical trials specialist vs research coordinator overview

Clinical Trials SpecialistResearch Coordinator
Yearly salary$74,910$48,974
Hourly rate$36.01$23.55
Growth rate6%6%
Number of jobs57,45865,406
Job satisfaction--
Most common degreeBachelor's Degree, 66%Bachelor's Degree, 65%
Average age4444
Years of experience22

What does a clinical trials specialist do?

A Clinical Trials specialist assist in the daily activities involved in clinical trials. This includes gathering facts, information, and observed data and helps analyze and interpret results. Clinic trials are essential in developing new medicines and vaccines needed for the safeguard of human health. Alongside this primary responsibility, it is also the clinical trial specialist's task to organize data, monitor laboratory equipment, and ensure all specimens needed for the trials are according to instructions.

What does a research coordinator do?

A research coordinator is responsible for assisting the development of research data from clinical trials and laboratory investigations under the supervision of a lead researcher or a research supervisor. In some cases, research coordinators conduct field investigations and analyze existing research materials upon understanding the scope and limitations of the study. They enter their findings and useful resources on the research database for reference to the research team. A research coordinator must have excellent communication skills, both written and oral, especially on gathering data and coordinating with other researchers for the progress and updates of the study.

Clinical trials specialist vs research coordinator salary

Clinical trials specialists and research coordinators have different pay scales, as shown below.

Clinical Trials SpecialistResearch Coordinator
Average salary$74,910$48,974
Salary rangeBetween $46,000 And $120,000Between $35,000 And $68,000
Highest paying CitySan Francisco, CABothell, WA
Highest paying stateCaliforniaConnecticut
Best paying companyExelixisBNP Paribas
Best paying industryPharmaceuticalHealth Care

Differences between clinical trials specialist and research coordinator education

There are a few differences between a clinical trials specialist and a research coordinator in terms of educational background:

Clinical Trials SpecialistResearch Coordinator
Most common degreeBachelor's Degree, 66%Bachelor's Degree, 65%
Most common majorBiologyPsychology
Most common collegeUniversity of Michigan - Ann ArborDuke University

Clinical trials specialist vs research coordinator demographics

Here are the differences between clinical trials specialists' and research coordinators' demographics:

Clinical Trials SpecialistResearch Coordinator
Average age4444
Gender ratioMale, 27.0% Female, 73.0%Male, 29.1% Female, 70.9%
Race ratioBlack or African American, 2.6% Unknown, 7.6% Hispanic or Latino, 15.2% Asian, 11.2% White, 62.9% American Indian and Alaska Native, 0.5%Black or African American, 2.6% Unknown, 7.6% Hispanic or Latino, 15.1% Asian, 10.2% White, 64.1% American Indian and Alaska Native, 0.5%
LGBT Percentage9%9%

Differences between clinical trials specialist and research coordinator duties and responsibilities

Clinical trials specialist example responsibilities.

  • Manage all clinical data and subject source documentation through the EDC system to verify compliance and subject eligibility.
  • Lead study data management activities for oncology trials in preparation for study close-out.
  • Review clinical study documents for completeness and compliance with protocol, FDA regulations, ICH and GCP guidelines.
  • Perform routine quality control (QC) of TMF and submit documents to ensure overall quality.
  • Review ICF and study reports and find discrepancies that are missed by CRO management.
  • Collect, review, approve and track in CTMS regulatory essential start-up and amendment documents.
  • Show more

Research coordinator example responsibilities.

  • Manage participant's records ensuring confidentiality as well as NIH specifications.
  • Manage all IRB submissions, sponsor communications, participate in monitoring visits, drug reconciliation and dispensing.
  • Recruit, screen, conduct psychometric examinations and collect data for pharmaceutical clinical trials in patients diagnose with Alzheimer's disease.
  • Maintain confidential information and appropriate ethical professionalism with highly sensitive personal health information; take part in IRB human subjects training.
  • Assist in preparation of grants, NIH progress reports, presentations, and manuscripts.
  • Ensure and maintain confidentiality, privacy and compliance of patient rights in accordance with HIPAA regulations and NVCI policies.
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Clinical trials specialist vs research coordinator skills

Common clinical trials specialist skills
  • Patients, 13%
  • Clinical Research, 10%
  • Clinical Trials, 9%
  • Informed Consent, 8%
  • FDA, 5%
  • Consent Forms, 4%
Common research coordinator skills
  • Patients, 11%
  • Informed Consent, 8%
  • Data Collection, 8%
  • IRB, 7%
  • Research Projects, 6%
  • Patient Care, 4%

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