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Senior clinical research coordinator vs study coordinator

The differences between senior clinical research coordinators and study 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 senior clinical research coordinator and a study coordinator. Additionally, a senior clinical research coordinator has an average salary of $60,458, which is higher than the $47,435 average annual salary of a study coordinator.

The top three skills for a senior clinical research coordinator include patients, IRB and informed consent. The most important skills for a study coordinator are patients, informed consent, and IRB.

Senior clinical research coordinator vs study coordinator overview

Senior Clinical Research CoordinatorStudy Coordinator
Yearly salary$60,458$47,435
Hourly rate$29.07$22.81
Growth rate6%6%
Number of jobs103,07714,929
Job satisfaction--
Most common degreeBachelor's Degree, 55%Bachelor's Degree, 61%
Average age4444
Years of experience22

What does a senior clinical research coordinator do?

A senior clinical research coordinator's main job is to conduct and administer clinical trials. From these clinical trials, they collect important data. They need to possess great verbal and written communication skills. They should be able to explain complex clinical research to almost any audience. They oversee the smooth functioning of the clinical trials and manage research budgets.

What does a study coordinator do?

Study coordinators oversee the entire process of clinical research from its inception to its completion. The coordinators make certain that human subjects are safe and well-protected. They identify the eligibility of the subject through clinical record screening and medical information extracting. It is their responsibility to maintain the regulatory documents based on the requirements of the Food and Drug Administration (FDA). They should develop skills and knowledge in clinical trials, study protocol, and patient care.

Senior clinical research coordinator vs study coordinator salary

Senior clinical research coordinators and study coordinators have different pay scales, as shown below.

Senior Clinical Research CoordinatorStudy Coordinator
Average salary$60,458$47,435
Salary rangeBetween $41,000 And $87,000Between $34,000 And $65,000
Highest paying CitySan Francisco, CAOakland, CA
Highest paying stateWashingtonConnecticut
Best paying companyArtemis HealthBloodworks Northwest
Best paying industryNon ProfitsHealth Care

Differences between senior clinical research coordinator and study coordinator education

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

Senior Clinical Research CoordinatorStudy Coordinator
Most common degreeBachelor's Degree, 55%Bachelor's Degree, 61%
Most common majorNursingNursing
Most common collegeUniversity of PennsylvaniaUniversity of Michigan - Ann Arbor

Senior clinical research coordinator vs study coordinator demographics

Here are the differences between senior clinical research coordinators' and study coordinators' demographics:

Senior Clinical Research CoordinatorStudy Coordinator
Average age4444
Gender ratioMale, 18.2% Female, 81.8%Male, 23.7% Female, 76.3%
Race ratioBlack or African American, 2.6% Unknown, 7.6% Hispanic or Latino, 15.3% Asian, 9.5% White, 64.6% American Indian and Alaska Native, 0.5%Black or African American, 2.6% Unknown, 7.6% Hispanic or Latino, 15.5% Asian, 8.9% White, 64.8% American Indian and Alaska Native, 0.5%
LGBT Percentage9%9%

Differences between senior clinical research coordinator and study coordinator duties and responsibilities

Senior clinical research coordinator example responsibilities.

  • Work closely with investigators in identifying and managing adverse events and report events according to FDA requirements.
  • Mentore and train employees on proper ICH and GCP clinical study procedures.
  • Leverage exceptional working knowledge of good clinical practice (GCP) and ICH regulatory instructions during the execution of clinical trials.
  • Co-Authore informed consents and consent patients while conducting information sessions with potential study subjects.
  • Authore study specific documents according to FDA regulations.
  • Conduct internal audits of oncology therapeutic trials for quality assurance purposes.
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Study coordinator example responsibilities.

  • Manage and analyze EKG and sleep data collect from subjects in confidential database.
  • Establish and maintain strong community partnerships to achieve HIV prevention objectives.
  • Conduct consent discussions and other study procedures per protocol and CFR and GCP guidelines.
  • Maintain strict patient confidentiality according to HIPPA regulations, GCP and ICH , 21 CFR and other regulatory documentation.
  • Maintain accurate IRB, regulatory and study documentation to insure compliance with protocol and good clinical practice guidelines.
  • Coordinate day-to-day study activities including data collection and statistical analysis, protocol development/implementation, IRB relations, and staff development.
  • Show more

Senior clinical research coordinator vs study coordinator skills

Common senior clinical research coordinator skills
  • Patients, 11%
  • IRB, 8%
  • Informed Consent, 7%
  • Data Collection, 6%
  • Coordinators, 5%
  • Patient Care, 5%
Common study coordinator skills
  • Patients, 14%
  • Informed Consent, 9%
  • IRB, 7%
  • Data Collection, 5%
  • FDA, 5%
  • Clinical Trials, 4%

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