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Clinical study manager vs study coordinator

The differences between clinical study managers 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 clinical study manager and a study coordinator. Additionally, a clinical study manager has an average salary of $78,195, which is higher than the $47,435 average annual salary of a study coordinator.

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

Clinical study manager vs study coordinator overview

Clinical Study ManagerStudy Coordinator
Yearly salary$78,195$47,435
Hourly rate$37.59$22.81
Growth rate6%6%
Number of jobs61,35214,929
Job satisfaction--
Most common degreeBachelor's Degree, 63%Bachelor's Degree, 61%
Average age4444
Years of experience22

What does a clinical study manager do?

A clinical study manager is primarily in charge of overseeing the efforts in conducting clinical studies, ensuring everything runs smoothly and efficiently. Their responsibilities include setting objectives, organizing budgets and schedules, establishing guidelines, delegating tasks, and developing strategies to optimize operations. They must also monitor the progress of the studies, conducting corrective measures when needed. Furthermore, as a clinical study manager, it is essential to lead and coordinate the workforce to reach goals, all while implementing the company's policies and regulations, including the study's vision and mission.

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.

Clinical study manager vs study coordinator salary

Clinical study managers and study coordinators have different pay scales, as shown below.

Clinical Study ManagerStudy Coordinator
Average salary$78,195$47,435
Salary rangeBetween $49,000 And $122,000Between $34,000 And $65,000
Highest paying CitySan Francisco, CAOakland, CA
Highest paying stateCaliforniaConnecticut
Best paying companyNeuralink IT SolutionsBloodworks Northwest
Best paying industryManufacturingHealth Care

Differences between clinical study manager and study coordinator education

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

Clinical Study ManagerStudy Coordinator
Most common degreeBachelor's Degree, 63%Bachelor's Degree, 61%
Most common majorBiologyNursing
Most common collegeUniversity of PennsylvaniaUniversity of Michigan - Ann Arbor

Clinical study manager vs study coordinator demographics

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

Clinical Study ManagerStudy Coordinator
Average age4444
Gender ratioMale, 35.0% Female, 65.0%Male, 23.7% Female, 76.3%
Race ratioBlack or African American, 2.6% Unknown, 7.6% Hispanic or Latino, 15.2% Asian, 10.8% White, 63.3% 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 clinical study manager and study coordinator duties and responsibilities

Clinical study manager example responsibilities.

  • Lead CRA training for Latin American, Asian and European to review GCP and protocol training.
  • Manage projects relate to commercialization and post market analysis for abdominal aortic aneurysm repair grafts as guided by FDA regulations.
  • Participate in CRF (EDC) design and CCG preparation.
  • Assist patients who suffer from depression, bipolar mood disorders, mental retardation, schizophrenia, post-traumatic disorder.
  • Contact patients regarding study information.
  • Develop study documents and facilitate IRB approvals.
  • Show more

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

Clinical study manager vs study coordinator skills

Common clinical study manager skills
  • GCP, 7%
  • Informed Consent, 7%
  • Oversight, 6%
  • Clinical Operations, 6%
  • ICH, 6%
  • Data Management, 5%
Common study coordinator skills
  • Patients, 14%
  • Informed Consent, 9%
  • IRB, 7%
  • Data Collection, 5%
  • FDA, 5%
  • Clinical Trials, 4%

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