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Study Manager Jobs (NOW HIRING)

Mobia Medical, Inc.

Clinical Study Manager

Fridley, MN · On-site

$110K - $160K/yr

About the role The Clinical Study Manager is a key member of the Clinical Affairs team, responsible for leading the operational execution and management of clinical studies that support the company ...

Arthrex

Clinical Study Manager

Naples, FL · On-site

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 ...

TEEMA

Study Manager - Mining & Metals

Phoenix, AZ · On-site

$90K - $145K/yr

Study Manager - Mining & Metals (PFS / FS) Location: Phoenix, AZ (Onsite) Role Type: Direct Hire | Senior Leadership The Opportunity Are you a strategic engineer who thrives in the Front-End of ...

ICON

Global Study Manager

Blue Bell, PA · On-site +1

Global Study Manager - Oncology - Home Based ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

Penumbra

Clinical Study Manager

General Summary The Clinical Study Manager provides leadership in the planning, design, and execution of clinical studies sponsored by Penumbra to assess safety and effectiveness of products. This ...

Syneoshealth

OR · On-site

Study Manager - Vaccine Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and ...

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 ...

Syneoshealth

OR · On-site

Study Manager - Oncology Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and ...

Spyglass Pharma

Clinical Study Manager

Aliso Viejo, CA · On-site

$140K - $160K/yr

Summary: The Clinical Study Manager (CSM) plays a key role in the planning and execution of SpyGlass Pharma's clinical trials. Working closely with the Director of Clinical Research and cross ...

Icon plc

Global Study Manager

Blue Bell, PA · On-site +1

Global Study Manager - Oncology - Home Based ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

Syneoshealth

OR

Study Manager - Ophthalmology Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs ...

Syneoshealth

OR

Study Manager - Immunology Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and ...

Intuitive

Sr. Clinical Study Manager

Sunnyvale, CA · On-site +1

The Clinical Study Manager-4 (CSM IV) role will develop and execute strategies for clinical and outcomes research studies to help regulatory approvals and key strategic evidence initiatives. As a ...

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$24.5K

$59.5K

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How much do study manager jobs pay per year?

As of May 31, 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

Mobia Medical, Inc.

Fridley, MN • On-site

$110K - $160K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 11 days ago

Job description

About Mobia Medical
Mobia Medical is a commercial-stage medtech company delivering breakthrough stroke recovery solutions. The company's Vivistim® Paired VNS™ Therapy is the first and only FDA-approved implantable solution designed to improve function in chronic ischemic stroke survivors with moderate to severe upper limb impairments. Vivistim® Paired VNS™ Therapy combines targeted vagus nerve stimulation with functional movement to promote neuroplasticity and improve the brain's ability to relearn motor skills. Mobia Medical is mobilizing patients, providers, and care partners to establish a better way forward in stroke care.
About the role
The Clinical Study Manager is a key member of the Clinical Affairs team, responsible for leading the operational execution and management of clinical studies that support the company's clinical development programs.
In this role, you will partner closely with Clinical, Regulatory, Data Management, Biostatistics, and cross-functional teams to ensure clinical studies are executed efficiently, compliantly, and with high-quality data outcomes. You will play a critical role in supporting feasibility, pivotal, and post-market studies while driving operational excellence and maintaining strong relationships with investigational sites and external partners.
What you'll do
Lead clinical study execution and operations
  • Manage clinical studies from start-up through close-out, ensuring timelines, deliverables, and study objectives are achieved
  • Develop and manage study timelines, enrollment plans, tracking tools, and operational deliverables
  • Support implementation of monitoring plans, enrollment initiatives, and risk mitigation strategies
  • Identify and proactively resolve operational, enrollment, compliance, and data quality challenges

Drive site management and investigator engagement
  • Support site qualification, initiation, interim monitoring, and close-out activities
  • Build and maintain strong relationships with investigators, research coordinators, and study personnel
  • Coordinate investigator meetings and site training activities
  • Ensure investigators and site staff are trained on protocols, investigational devices, EDC systems, and regulatory requirements
  • Support enrollment and retention initiatives while ensuring protocol adherence and informed consent compliance

Ensure data quality and regulatory compliance
  • Ensure accurate, complete, and timely collection of clinical trial data
  • Monitor study metrics and trends to identify risks or quality concerns
  • Identify protocol deviations, safety concerns, and noncompliance issues and ensure appropriate escalation and resolution
  • Support audit and inspection readiness activities
  • Assist with preparation of study reports, annual reports, and clinical documentation submissions

Collaborate cross-functionally and support continuous improvement
  • Partner with Data Management, Biostatistics, Regulatory, and Clinical teams to support study execution and reporting
  • Manage and oversee CROs, vendors, and external study partners to ensure high-quality deliverables
  • Contribute to process improvement initiatives within Clinical Operations

Qualifications
What you bring:
  • Bachelor's degree in life sciences, nursing, engineering, or related scientific discipline required
  • Advanced degree preferred
  • 5+ years of clinical research experience in medical device, biotechnology, or pharmaceutical industries
  • 3+ years of clinical study management or clinical operations experience
  • Experience supporting feasibility, pivotal, and/or post-market clinical studies
  • Strong understanding of clinical trial operations, site management, and study execution

Preferred qualifications:
  • Experience supporting multicenter clinical trials
  • Experience managing CROs and external vendors
  • Strong knowledge of FDA regulations, GCP, and clinical research compliance requirements
  • Experience with EDC systems, CTMS platforms, and clinical trial tracking tools

You'll thrive in this role if you are:
  • Highly organized with strong project management and prioritization skills
  • A collaborative team player who works effectively across cross-functional groups
  • A proactive problem solver who can identify and mitigate study risks
  • Detail-oriented with a strong commitment to data quality and regulatory compliance
  • An effective communicator who builds trusted relationships with study sites and internal stakeholders

Equal Opportunity Employer
Mobia Medical provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
Benefits
Mobia Medical provides a comprehensive benefits program to employees. It includes medical, dental and vision plans along with an FSA. Employees may participate in the company 401(k) plan with company matching. The company offers an unlimited Paid Time Off (PTO) program and approximately 18 paid company holidays per year.
Apply now
The pay range for this role is:
110,000 - 160,000 USD per year (US National)

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