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Clinical Research Study Manager Jobs (NOW HIRING)

Axogen

Clinical Study Manager

Tampa, FL

Job Summary of the Clinical Study Manager The Clinical Study Manager (CSM) is accountable for the ... Minimum 5 years of industrysponsored clinical research experience. * Demonstrated experience ...

Tenet Health

Clinical Research Coordinator

Delray Beach, FL · On-site

$22.75 - $30.25/hr

Full Time, Days Onsite position at Delray Medical Center The Clinical Research Coordinator (CRC ... Assists with coordination of overall study management of participants. This includes patient's care ...

Tenet Health

Clinical Research Coordinator

Delray Beach, FL · On-site

$22.75 - $30.25/hr

Full Time, Days Onsite position at Delray Medical Center The Clinical Research Coordinator (CRC ... Assists with coordination of overall study management of participants. This includes patient's care ...

Uw

CTU Research Study Assistant

Seattle, WA · Hybrid

$22 - $30.25/hr

... industry sponsored clinical research studies. The CTU supports and manages Human Subjects ... regulatory, and financial oversight to ensure efficient execution of studies with the highest ...

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$49K

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$189K

How much do clinical research study manager jobs pay per year?

As of Jun 8, 2026, the average yearly pay for clinical research study manager in the United States is $107,336.00, according to ZipRecruiter salary data. Most workers in this role earn between $81,000.00 and $122,500.00 per year, depending on experience, location, and employer.

What does a Clinical Research Study Manager do?

A Clinical Research Study Manager oversees the planning, execution, and completion of clinical trials to ensure they are conducted ethically and in compliance with regulatory standards. They coordinate with research teams, manage budgets and timelines, and ensure accurate data collection and reporting. Their role is crucial in ensuring that clinical studies run smoothly and produce reliable results that can be used for regulatory submissions or scientific publications.

What are the key skills and qualifications needed to thrive as a Clinical Research Study Manager, and why are they important?

To thrive as a Clinical Research Study Manager, you need expertise in clinical trial management, regulatory compliance, and protocol development, often supported by a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and certifications such as GCP (Good Clinical Practice) are typically required. Strong organizational, leadership, and communication skills help manage cross-functional teams and ensure smooth study execution. These skills and qualifications are crucial for maintaining study integrity, meeting regulatory standards, and delivering successful clinical trial outcomes.

What are some common challenges faced by Clinical Research Study Managers in coordinating multi-site studies?

Clinical Research Study Managers often encounter challenges in ensuring consistent protocol adherence and data integrity across multiple study sites. Coordinating communication between site teams, managing timelines, and troubleshooting unexpected issues such as recruitment delays or regulatory hurdles are frequent tasks. Successful managers use strong organizational skills and proactive planning to mitigate these challenges, and often rely on regular meetings and digital tools to keep all stakeholders aligned. Establishing clear processes and fostering open communication are key to overcoming these complexities and ensuring study success.

What is the difference between Clinical Research Study Manager vs Clinical Research Coordinator?

AspectClinical Research Study ManagerClinical Research Coordinator
CredentialsBachelor's degree, often with experience in project managementBachelor's degree in health sciences or related field, certification optional
Work EnvironmentOversees multiple studies, manages teams, and coordinates with sponsorsHandles daily study activities, patient interactions, and data collection
Employer & IndustryPharmaceutical companies, CROs, academic institutionsHospitals, clinics, research sites
Search & Comparison IntentUnderstanding managerial roles, responsibilities, and qualificationsFocus on operational tasks and patient management

The Clinical Research Study Manager typically oversees multiple studies, manages teams, and liaises with sponsors, requiring project management skills. In contrast, the Clinical Research Coordinator handles daily study activities, patient interactions, and data collection at research sites. Both roles are essential in clinical research but differ in scope and responsibilities.

More about Clinical Research Study Manager jobs
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Clinical Research Study Manager jobs near you
RN Clinical Research Study PRN

RN Clinical Research Study PRN

CommonSpirit Health

Loveland, OH

$38/hr

Part-time, Per diem

Posted 7 days ago

CommonSpirit Health rating

7.1

Company rating: 7.1 out of 10

Based on 503 frontline employees who took The Breakroom Quiz

372nd of 869 rated healthcare providers

Job description

At CHI Health, we're dedicated to making a difference in people's lives every day.   We are offering a PRN opportunity on either day and night working on a clinical research study at Cincinnati Children's Hospital Medical Center.

 

Registered Nurse / Clinical Research Study on a PRN basis.

We currently are  seeking several quality, self-driven RN's to work in  In-Patient Clinical Research Studies at Cincinnati Children's Hospital Medical Center in Cincinnati, OH.

  • Shifts are guaranteed and scheduling is very flexible.
  • $38 per hour paid weekly.
  • Part-time and up to 40 hours per week are available for this assignment. 

  • Graduate of an accredited school of nursing
  • Currently licensed to practice in Ohio.
  • One year of RN nursing experience required

#RN_rx.

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