ZipRecruiter

Log In

1

Study Manager Jobs (NOW HIRING)

Axogen

Clinical Study Manager

Tampa, FL · On-site

Job Summary of the Clinical Study Manager The Clinical Study Manager (CSM) is accountable for the end-to-end operational leadership of an Axogen-sponsored randomized controlled trial (RCT) and other ...

ARTIDIS

Clinical Study Manager

Houston, TX

The Clinical Study Manager is an integral part of the Clinical Operations Team which manages planned and ongoing clinical studies. The Clinical Study Manager is responsible for overseeing the ...

ARTIDIS

Clinical Study Manager

Houston, TX · On-site

The Clinical Study Manager is an integral part of the Clinical Operations Team which manages planned and ongoing clinical studies. The Clinical Study Manager is responsible for overseeing the ...

ARTHREX

Clinical Study Manager

Naples, FL

Clinical Study Manager Arthrex, Inc. is a global medical device company and a leader in new product development and medical education in orthopedics. Arthrex is actively searching for a Clinical ...

Danaher

Senior Clinical Study Manager

The Senior Clinical Study Manager is responsible for clinical trial execution within the US and EU regions for Leica Biosystems. This role will specifically support Leica Biosystems, an operating ...

Danaher

Senior Clinical Study Manager

OR · On-site +1

The Senior Clinical Study Manager will be responsible for clinical trial execution within the US for Danaher Diagnostics. This role will specifically support Radiometer Medical, an operating company ...

Cordis

Clinical Study Manager

Irvine, CA · On-site +1

$114.95K - $165K/yr

Responsibilities The Clinical Study Manager (CSM) is responsible for the operational management and execution of clinical trials, ensuring studies are delivered on time, within budget, and in ...

Danaher

Senior Clinical Study Manager

OR · Remote

The Senior Clinical Study Manager is responsible for clinical trial execution within the US and EU regions for Leica Biosystems. This role will specifically support Leica Biosystems, an operating ...

next page

Showing results 1-20

People also search for

All JobsStudy JobsStudy Manager Jobs

Study Manager information

See salary details

$24.5K

$59.5K

$116K

How much do study manager jobs pay per year?

As of Jun 1, 2026, the average yearly pay for study manager in the United States is $59,525.00, according to ZipRecruiter salary data. Most workers in this role earn between $42,000.00 and $68,500.00 per year, depending on experience, location, and employer.

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

To thrive as a Study Manager, you need a solid background in clinical research, regulatory compliance, and project management, often supported by a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and GCP certification is typically required. Strong organizational skills, attention to detail, and effective communication are essential soft skills for coordinating teams and stakeholders. These qualifications ensure the successful planning, execution, and oversight of clinical studies within regulatory and timeline requirements.

How does a Study Manager typically collaborate with cross-functional teams during the course of a clinical trial?

As a Study Manager, you'll work closely with cross-functional teams including clinical research associates, data managers, regulatory affairs, and biostatisticians to ensure the trial progresses smoothly and meets regulatory requirements. Regular meetings, status updates, and shared project management tools facilitate clear communication and timely issue resolution. You will often serve as the central point of contact, coordinating tasks and resolving conflicts between departments to keep the study on track. Collaboration skills are essential, as you’ll need to balance input from multiple stakeholders while maintaining study timelines and quality standards.

What does a Study Manager do?

A Study Manager is responsible for overseeing the planning, execution, and completion of research studies, often in clinical or academic settings. They coordinate between various stakeholders, including research teams, sponsors, and regulatory authorities, to ensure studies are conducted efficiently and in compliance with relevant guidelines. Study Managers manage timelines, budgets, and resources, while also handling documentation and reporting requirements. Their role is critical to ensuring that studies meet their scientific objectives and adhere to ethical standards.
More about Study Manager jobs
What cities are hiring for Study Manager jobs? Cities with the most Study Manager job openings:
What are the most commonly searched types of Study jobs? The most popular types of Study jobs are:
What states have the most Study Manager jobs? States with the most job openings for Study Manager jobs include:
Study Manager jobs near you
Infographic showing various Study Manager job openings in the United States as of May 2026, with employment types broken down into 1% As Needed, 83% Full Time, 14% Part Time, 1% Contract, and 1% Nights. Highlights an 90% Physical, and 10% Remote job distribution, with an average salary of $59,525 per year, or $28.6 per hour.
Clinical Study Manager

Clinical Study Manager

Axogen

Tampa, FL • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 22 days ago

Job description

Axogen is committed to building and maintaining a strong and gratifying company culture that fosters professional growth. Our hands-on and personal approach makes transitioning to a new job a seamless and enjoyable process. Most benefits are effective on day one!
Axogen is an equal opportunity employer and does not discriminate against applicants on the basis of race, color, creed, religion, ancestry, age, sex, marital status, national origin, disability or veteran status.
Why you'll love working at Axogen:
  • Friendly, open, and fun team culture that values unique perspectives
  • Company-wide dedication to profoundly impacting patients' lives
  • Comprehensive, high-quality benefits package effective on date of hire
  • Educational assistance available for all employees
  • Matching 401(k) retirement plan
  • Paid holidays, including floating holidays, to be used at your discretion
  • Employee Stock Purchase Plan
  • Referral incentive program

Axogen Mission and Business Purpose
Our business purpose is to restore health and improve quality of life by making restoration of peripheral nerve function an expected standard of care. We aim to lead the markets we serve by always requiring the solutions we offer patients and caregivers provide an improved benefit-to-risk profile as compared to existing standards of care. To ensure we deliver improved benefit-to-risk solutions, we will guide and expect the market and design requirement specifications underlying our engineering, business development, and clinical research activities, objectively target advancements in standards of care.
Job Summary of the Clinical Study Manager
The Clinical Study Manager (CSM) is accountable for the end-to-end operational leadership of an Axogen-sponsored randomized controlled trial (RCT) and other complex prospective clinical studies conducted in highly regulated environments, including biologics, combination products, and medical devices. This role is intended for a highly experienced clinical operations professional who can independently own study execution, serve as the operational authority for an assigned trial, and act as a role model for CRAs, vendors, and cross-functional partners. The CSM is responsible for ensuring exceptional execution quality, data integrity, and inspection readiness while maintaining the highest standards of ethics and Good Clinical Practice (GCP).
Requirements of the Clinical Study Manager
  • Bachelor's degree or higher in a scientific, medical, or engineering discipline (or equivalent experience).
  • Minimum 5 years of industry-sponsored clinical research experience.
  • Demonstrated experience leading complex prospective interventional studies, with RCT experience strongly preferred.
  • Experience conducting studies in biologics, combination products, and/or medical devices.
  • Proven track record of maintaining high data integrity, compliance, and inspection readiness.
  • Strong working knowledge of ICH-GCP and global regulatory requirements.
  • Willingness and ability to travel up to 50%.

Responsibilities of the Clinical Study Manager
The specific duties of the Clinical Study Manager include but are not limited to:
Clinical Operations Leadership
  • Lead the planning, start-up, execution, monitoring, and close out of large, complex prospective clinical studies, including RCTs.
  • Serve as the study level operational owner, accountable for timelines, quality, compliance, and execution excellence.
  • Translate protocol intent and regulatory requirements into robust, executable clinical operations strategies.

Study Planning & Execution
  • Develop and execute comprehensive:
    • Clinical Operations Plans
    • Monitoring Plans
    • Vendor Oversight Plans
    • Recruitment and retention strategies
    • Study timelines, budgets, and resourcing plans
    • Ensure study conduct aligns with protocol, SAP, investigational plan, and regulatory commitments.

Quality, Compliance, and Inspection Readiness
  • Ensure continuous compliance with:
    • ICH-GCP
    • FDA and OUS regulatory requirements
    • Internal SOPs and quality standards
  • Proactively identify and mitigate risks to subject safety, data integrity, and regulatory compliance.
  • Lead and support audit and inspection readiness, responses, and CAPA development.

Vendor & Site Oversight
  • Lead selection, onboarding, and oversight of CROs and other clinical vendors.
  • Drive vendor performance through KPIs, issue escalation, and corrective actions.
  • Oversee site selection, activation, and ongoing performance, including the performance of on-site visits, enrollment tracking, monitoring quality, protocol adherence.

Team Leadership & Mentorship
  • Provide leadership, mentoring, and professional guidance to CRAs and study team members.
  • Serve as a role model for best-in-class clinical operations conduct, documentation quality, and ethical decision-
  • Contribute to SOPs, work instructions, templates, and training materials.

Location
111 West Oak Ave., Tampa, FL 33602
#LI-AC1
Benefits/Compensation
This position is eligible for an annual bonus.
Benefits offered for this position include Health, Dental, Vision, Matching 401K, Paid Time Off, 9 Paid Holidays + 3 Floating Holidays, Dependent Care Flexible Spending Accounts, Medical Flexible Spending Accounts, Tuition Reimbursement, Paid Parental Leave, Paid Caregiver Leave, Basic Life Insurance, Supplemental Life Insurance, Employee Stock Purchase Plan, and Disability Insurance, as described in more detail in summary plan descriptions.
Salary Range
$113,903-$142,378 USD
Axogen follows healthcare system guidelines with respect to credentialing, vaccinations and other employment/compliance related requirements, as well as CDC guidance. Axogen reserves the right to amend its policies from time to time in its sole discretion.

Apply