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Clinical trials specialist vs senior program coordinator

The differences between clinical trials specialists and senior program coordinators can be seen in a few details. Each job has different responsibilities and duties. While it typically takes 1-2 years to become a clinical trials specialist, becoming a senior program coordinator takes usually requires 2-4 years. Additionally, a clinical trials specialist has an average salary of $74,910, which is higher than the $74,468 average annual salary of a senior program coordinator.

The top three skills for a clinical trials specialist include patients, clinical research and clinical trials. The most important skills for a senior program coordinator are alumni, excellent organizational, and powerpoint.

Clinical trials specialist vs senior program coordinator overview

Clinical Trials SpecialistSenior Program Coordinator
Yearly salary$74,910$74,468
Hourly rate$36.01$35.80
Growth rate6%7%
Number of jobs57,45880,629
Job satisfaction--
Most common degreeBachelor's Degree, 66%Bachelor's Degree, 68%
Average age4444
Years of experience24

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 senior program coordinator do?

A senior program coordinator is primarily in charge of spearheading and managing programs, ensuring everything runs smoothly and efficiently. Their responsibilities revolve around participating in setting goals and objectives, securing funding and sponsors, overseeing the workforce, and even establishing guidelines. They may also facilitate communication within the company and liaise with external parties. Furthermore, as a senior program coordinator, it is essential to lead and encourage the teams to reach goals, all while implementing the company's policies and regulations, including its vision and mission.

Clinical trials specialist vs senior program coordinator salary

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

Clinical Trials SpecialistSenior Program Coordinator
Average salary$74,910$74,468
Salary rangeBetween $46,000 And $120,000Between $46,000 And $120,000
Highest paying CitySan Francisco, CASan Francisco, CA
Highest paying stateCaliforniaCalifornia
Best paying companyExelixisMayo Clinic
Best paying industryPharmaceutical-

Differences between clinical trials specialist and senior program coordinator education

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

Clinical Trials SpecialistSenior Program Coordinator
Most common degreeBachelor's Degree, 66%Bachelor's Degree, 68%
Most common majorBiologyBusiness
Most common collegeUniversity of Michigan - Ann ArborStanford University

Clinical trials specialist vs senior program coordinator demographics

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

Clinical Trials SpecialistSenior Program Coordinator
Average age4444
Gender ratioMale, 27.0% Female, 73.0%Male, 29.5% Female, 70.5%
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, 11.5% Unknown, 4.2% Hispanic or Latino, 16.7% Asian, 5.4% White, 61.4% American Indian and Alaska Native, 0.7%
LGBT Percentage9%16%

Differences between clinical trials specialist and senior program 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

Senior program coordinator example responsibilities.

  • Manage co-op vendor and provide overall program direction for Toyota dealers and regional offices nationwide.
  • Report metrics associate with assign compounds to QA management, clinical development clinical development staff, and contract research organization staff.
  • Participate at PPT's and participate in the development of IEP's and strategies to meet IEP objectives.
  • Coordinate RFP policies and processes for all grant programs to ensure consistency.
  • Collaborate with home inspector to create scope of work, prepare RFP s to secure construction bid quotes from rehabilitation contractors.
  • Schedule and facilitate all IEP meetings, gathering information, inviting participants and encouraging parent participation.
  • Show more

Clinical trials specialist vs senior program coordinator skills

Common clinical trials specialist skills
  • Patients, 13%
  • Clinical Research, 10%
  • Clinical Trials, 9%
  • Informed Consent, 8%
  • FDA, 5%
  • Consent Forms, 4%
Common senior program coordinator skills
  • Alumni, 7%
  • Excellent Organizational, 6%
  • PowerPoint, 6%
  • SR, 5%
  • Data Entry, 5%
  • HR, 5%

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