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Clinical study manager vs clinical research coordinator

The differences between clinical study managers and clinical research 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 clinical research coordinator. Additionally, a clinical study manager has an average salary of $78,195, which is higher than the $52,459 average annual salary of a clinical research coordinator.

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

Clinical study manager vs clinical research coordinator overview

Clinical Study ManagerClinical Research Coordinator
Yearly salary$78,195$52,459
Hourly rate$37.59$25.22
Growth rate6%6%
Number of jobs61,352102,960
Job satisfaction--
Most common degreeBachelor's Degree, 63%Bachelor's Degree, 60%
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 clinical research coordinator do?

A clinical research coordinator is a healthcare professional responsible for administering clinical trials of drugs or medications. Clinical research coordinators work under the supervision of clinical research managers to collect data and help inform trial participants about the study's objectives. They must ensure that these trials have met all regulations, including drug safety, government regulations, and the organization's code of ethics. Clinical research coordinators must obtain a bachelor's degree in nursing and have at least two years of healthcare experience.

Clinical study manager vs clinical research coordinator salary

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

Clinical Study ManagerClinical Research Coordinator
Average salary$78,195$52,459
Salary rangeBetween $49,000 And $122,000Between $37,000 And $72,000
Highest paying CitySan Francisco, CARichmond, CA
Highest paying stateCaliforniaWashington
Best paying companyNeuralink IT SolutionsGenentech
Best paying industryManufacturingHealth Care

Differences between clinical study manager and clinical research coordinator education

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

Clinical Study ManagerClinical Research Coordinator
Most common degreeBachelor's Degree, 63%Bachelor's Degree, 60%
Most common majorBiologyNursing
Most common collegeUniversity of PennsylvaniaDuke University

Clinical study manager vs clinical research coordinator demographics

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

Clinical Study ManagerClinical Research Coordinator
Average age4444
Gender ratioMale, 35.0% Female, 65.0%Male, 20.0% Female, 80.0%
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, 2.5% Unknown, 7.5% Hispanic or Latino, 14.7% Asian, 10.7% White, 64.0% American Indian and Alaska Native, 0.5%
LGBT Percentage9%9%

Differences between clinical study manager and clinical research 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

Clinical research coordinator example responsibilities.

  • Assess study participants for adverse reactions or complications and manage side effects of chemotherapy and other study relate drugs.
  • Establish and maintain strong community partnerships to achieve HIV prevention objectives.
  • Direct acquisition and analysis of functional MRI research data following GCP and FDA regulations
  • Prepare and maintain IRB and regulatory documentation for various research projects and consent patients for clinical research.
  • Facilitate constant communication between principal investigators, oncology nurses, and patients to address concerns and maximize eligibility and enrollment.
  • Schedule patient for study procedures; initiate/coordinate drug orders, laboratory procedures and treatments for patients base on standing protocol orders.
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Clinical study manager vs clinical research coordinator skills

Common clinical study manager skills
  • GCP, 7%
  • Informed Consent, 7%
  • Oversight, 6%
  • Clinical Operations, 6%
  • ICH, 6%
  • Data Management, 5%
Common clinical research coordinator skills
  • Patients, 11%
  • Informed Consent, 10%
  • IRB, 7%
  • Data Collection, 5%
  • Research Projects, 4%
  • Patient Care, 4%

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