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Clinical trial coordinator vs clinical trials associate

The differences between clinical trial coordinators and clinical trials 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 trial coordinator and a clinical trials associate. Additionally, a clinical trials associate has an average salary of $74,952, which is higher than the $50,720 average annual salary of a clinical trial coordinator.

The top three skills for a clinical trial coordinator include clinical trials, patients and informed consent. The most important skills for a clinical trials associate are informed consent, patients, and clinical operations.

Clinical trial coordinator vs clinical trials associate overview

Clinical Trial CoordinatorClinical Trials Associate
Yearly salary$50,720$74,952
Hourly rate$24.38$36.03
Growth rate6%6%
Number of jobs64,85955,487
Job satisfaction--
Most common degreeBachelor's Degree, 62%Bachelor's Degree, 62%
Average age4444
Years of experience22

What does a clinical trial coordinator do?

A clinical trial coordinator is responsible for assisting in medical trials and clinical research studies. Clinical trial coordinators support the whole operational process of medical research from its conceptualization until the final outputs. They manage the adequacy of tools and equipment, ensuring the cleanliness and orderliness of the facilities to prevent potential hazards and delays in laboratory testing. A clinical trial coordinator must have excellent communication and organizational skills, especially in writing progress reports and securing the acquired laboratory samples.

What does a clinical trials associate do?

A clinical trial associate is in charge of coordinating and executing clinical trial operations, ensuring to meet all goals within budgets and deadlines. Their responsibilities revolve around preparing and processing necessary documentation and certifications, submitting requirements to government agencies, distributing essential materials within the clinical teams, and reviewing study sheets, ensuring every paperwork is complete and accurate. Furthermore, as a clinical trial associate, it is vital to lead while implementing the company's policies and regulations, including its vision and mission.

Clinical trial coordinator vs clinical trials associate salary

Clinical trial coordinators and clinical trials associates have different pay scales, as shown below.

Clinical Trial CoordinatorClinical Trials Associate
Average salary$50,720$74,952
Salary rangeBetween $35,000 And $72,000Between $46,000 And $121,000
Highest paying CityBerkeley, CASan Francisco, CA
Highest paying stateCaliforniaCalifornia
Best paying companyMohawk Valley Health SystemDorsey & Whitney
Best paying industryHealth CarePharmaceutical

Differences between clinical trial coordinator and clinical trials associate education

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

Clinical Trial CoordinatorClinical Trials Associate
Most common degreeBachelor's Degree, 62%Bachelor's Degree, 62%
Most common majorNursingBiology
Most common collegeUniversity of PennsylvaniaUniversity of Pennsylvania

Clinical trial coordinator vs clinical trials associate demographics

Here are the differences between clinical trial coordinators' and clinical trials associates' demographics:

Clinical Trial CoordinatorClinical Trials Associate
Average age4444
Gender ratioMale, 23.9% Female, 76.1%Male, 25.3% Female, 74.7%
Race ratioBlack or African American, 2.6% Unknown, 7.6% Hispanic or Latino, 15.2% Asian, 10.5% White, 63.6% American Indian and Alaska Native, 0.5%Black or African American, 2.5% Unknown, 7.4% Hispanic or Latino, 13.9% Asian, 13.4% White, 62.3% American Indian and Alaska Native, 0.5%
LGBT Percentage9%9%

Differences between clinical trial coordinator and clinical trials associate duties and responsibilities

Clinical trial coordinator example responsibilities.

  • Establish and maintain strong community partnerships to achieve HIV prevention objectives.
  • Coordinate grant and IRB renewals and submissions; and preparation of publications, study protocols and manuals of operations.
  • Develop a GUI tool for volume & surface area of lesion/hematoma/edema in stroke MRI.
  • Privilege to negotiation principles from the consumers stand point within the divisions of: oncology, bariatric, cosmetic & cardiovascular.
  • Compose SPSS syntax to simplify data import process, reducing the time require from a full day to a few minutes.
  • Analyze collected data using SPSS to determine possible significant findings.
  • Show more

Clinical trials associate example responsibilities.

  • Manage trial master files and study document to meet GCP/ICH and internal guidelines for records retention.
  • Audit TMF to ensure all require regulatory documentation are collected and lead.
  • Work closely with investigators to recruit eligible patients to clinical protocols, manage data collection and preparation.
  • Preform ICF customization in accordance with ICH guidelines, GCP s and local regulatory requirements.
  • Support the setup, data entry and QC of the system to ensure accuracy and quality of data.
  • Monitor clinical data and resolve inconsistencies according to FDA regulations and ICF guidelines.
  • Show more

Clinical trial coordinator vs clinical trials associate skills

Common clinical trial coordinator skills
  • Clinical Trials, 12%
  • Patients, 11%
  • Informed Consent, 10%
  • IRB, 4%
  • Meeting Minutes, 4%
  • FDA, 4%
Common clinical trials associate skills
  • Informed Consent, 9%
  • Patients, 7%
  • Clinical Operations, 6%
  • FDA, 6%
  • Consent Forms, 5%
  • TMF, 5%

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