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Clinical trials specialist vs research project coordinator

The differences between clinical trials specialists and research project 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 project coordinator. Additionally, a clinical trials specialist has an average salary of $74,910, which is higher than the $48,683 average annual salary of a research project coordinator.

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

Clinical trials specialist vs research project coordinator overview

Clinical Trials SpecialistResearch Project Coordinator
Yearly salary$74,910$48,683
Hourly rate$36.01$23.41
Growth rate6%6%
Number of jobs57,45867,800
Job satisfaction--
Most common degreeBachelor's Degree, 66%Bachelor's Degree, 67%
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 project coordinator do?

Research Project Coordinators take on a lead role in maintaining and creating processes that support the execution of a research project. Their duties include researching governance requirements, preparing for contract bidding, manage budgeting of a project to meet a specified timeline, and present findings of a project to all stakeholders involved. The Research Project Coordinator will also support administrative tasks, including producing corporate reports, organizing committee meetings, and developing a research database to track active milestones achieved.

Clinical trials specialist vs research project coordinator salary

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

Clinical Trials SpecialistResearch Project Coordinator
Average salary$74,910$48,683
Salary rangeBetween $46,000 And $120,000Between $36,000 And $65,000
Highest paying CitySan Francisco, CAMiddletown, CT
Highest paying stateCaliforniaConnecticut
Best paying companyExelixisDignity Health
Best paying industryPharmaceuticalProfessional

Differences between clinical trials specialist and research project coordinator education

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

Clinical Trials SpecialistResearch Project Coordinator
Most common degreeBachelor's Degree, 66%Bachelor's Degree, 67%
Most common majorBiologyPsychology
Most common collegeUniversity of Michigan - Ann ArborDuke University

Clinical trials specialist vs research project coordinator demographics

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

Clinical Trials SpecialistResearch Project Coordinator
Average age4444
Gender ratioMale, 27.0% Female, 73.0%Male, 37.8% Female, 62.2%
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, 2.5% Unknown, 7.4% Hispanic or Latino, 13.9% Asian, 13.3% White, 62.4% American Indian and Alaska Native, 0.5%
LGBT Percentage9%9%

Differences between clinical trials specialist and research project 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 project coordinator example responsibilities.

  • Manage study documentation throughout study life cycle including IRB annual renewals, modifications, patient study charts and regulatory binder.
  • Recommend administrative revisions to IRB submit studies including inform consent documents.
  • Demonstrate small molecule are protective against DNA damage in mouse model of melanoma.
  • Conduct analysis using SPSS which result in developing a new software for students to selecting college.
  • Conduct primary research through interviews with Boston area travelers and analyze raw data into reports via SPSS.
  • Maintain FDA correspondence and government documentation.
  • Show more

Clinical trials specialist vs research project 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 project coordinator skills
  • Data Collection, 12%
  • Patients, 9%
  • Project Management, 6%
  • Public Health, 5%
  • IRB, 5%
  • Data Analysis, 4%

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