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Clinical trials specialist vs clinical research associate

The differences between clinical trials specialists and clinical research associates 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 clinical research associate. Additionally, a clinical trials specialist has an average salary of $74,910, which is higher than the $62,966 average annual salary of a clinical research associate.

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

Clinical trials specialist vs clinical research associate overview

Clinical Trials SpecialistClinical Research Associate
Yearly salary$74,910$62,966
Hourly rate$36.01$30.27
Growth rate6%6%
Number of jobs57,45894,336
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 clinical research associate do?

A clinical research associate is responsible for assisting medical professionals in clinical trials and conducting research studies on medications and medical procedures. Clinical research associates monitor the research materials, ensuring its safety and reliability through trial procedures, writing comprehensive reports of results, and disseminating information across the concerned parties. They also provide recommendations on improving clinical processes, reiterating protocol requirements, and maintaining strict confidentiality of the trial subjects. A clinical research associate must have extensive knowledge of the medical industry, including its disciplines and principles, to perform duties accurately under minimal supervision.

Clinical trials specialist vs clinical research associate salary

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

Clinical Trials SpecialistClinical Research Associate
Average salary$74,910$62,966
Salary rangeBetween $46,000 And $120,000Between $43,000 And $91,000
Highest paying CitySan Francisco, CASan Francisco, CA
Highest paying stateCaliforniaCalifornia
Best paying companyExelixisMeta
Best paying industryPharmaceuticalPharmaceutical

Differences between clinical trials specialist and clinical research associate education

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

Clinical Trials SpecialistClinical Research Associate
Most common degreeBachelor's Degree, 66%Bachelor's Degree, 65%
Most common majorBiologyBiology
Most common collegeUniversity of Michigan - Ann ArborUniversity of Pennsylvania

Clinical trials specialist vs clinical research associate demographics

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

Clinical Trials SpecialistClinical Research Associate
Average age4444
Gender ratioMale, 27.0% Female, 73.0%Male, 28.3% Female, 71.7%
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, 13.7% Asian, 13.0% White, 62.9% American Indian and Alaska Native, 0.5%
LGBT Percentage9%9%

Differences between clinical trials specialist and clinical research associate 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

Clinical research associate example responsibilities.

  • Manage, schedule and train up to 15 CRAs.
  • Recruit patients, attain patient inform consent form, educate subjects on compliance, and ensure patient safety per ICH guidelines.
  • Manage site TMF to ensure communication requirements adherence
  • Manage CRO and regional monitor to complete close out activities, including device accountability management.
  • Manage regional academic and community base oncology practices as the primary contact for all communications and support.
  • Manage the monitoring CRO and the data clean-up efforts for a 510k submission and interim/annual study reports by effectively collaborating cross-functionally.
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Clinical trials specialist vs clinical research associate skills

Common clinical trials specialist skills
  • Patients, 13%
  • Clinical Research, 10%
  • Clinical Trials, 9%
  • Informed Consent, 8%
  • FDA, 5%
  • Consent Forms, 4%
Common clinical research associate skills
  • Patients, 9%
  • Informed Consent, 7%
  • CRA, 6%
  • Clinical Trials, 6%
  • Clinical Trial Management, 5%
  • Oncology, 4%

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