ZipRecruiter

Log In

1

Clinical Study Assistant Jobs (NOW HIRING)

Mobia Medical, Inc.

Clinical Study Manager

Fridley, MN · On-site

$110K - $160K/yr

Support audit and inspection readiness activities * Assist with preparation of study reports, annual reports, and clinical documentation submissions Collaborate cross-functionally and support ...

Uw

CTU Research Study Assistant

Seattle, WA · Hybrid

$22 - $30.25/hr

... Study Assistant to join their team. The purpose of this position is to support the research ... The Clinical Trials Unit (CTU) at the University of Washington supports these investigators by ...

New

PSI CRO

Clinical Study Coordinator

Cleveland, TN · On-site

We understand what clinical study sites need and our overall mission is to support sites in ... visit to assist in a smooth patient flow at research visits., general study conduct tasks ...

Medacta USA, Inc.

Clinical Study Manager

Franklin, TN · On-site

Experience with study and site level management of clinical trials, including but not limited ... * Assist in reporting and follow-up of clinical unexpected and Serious Adverse Event (SAE ...

New

Medacta USA, Inc.

Clinical Study Manager

Franklin, TN · On-site

Experience with study and site level management of clinical trials, including but not limited ... * Assist in reporting and follow-up of clinical unexpected and Serious Adverse Event (SAE ...

New

DiaSorin

Clinical Study Coordinator

Austin, TX · On-site

Collection and analysis of experimental data generated in-house and externally * Assist with site qualification processes and support monitoring of external clinical sites in accordance with study ...

DiaSorin

Clinical Study Coordinator

Austin, TX · On-site

Collection and analysis of experimental data generated in-house and externally * Assist with site qualification processes and support monitoring of external clinical sites in accordance with study ...

On-Board Services

Clinical Lab Assistant

Stamford, CT · On-site

$25 - $32/hr

Major Duties and Responsibilities Prepare documents for clinical studies, assist in study material preparation, interview and administer informed consent to clinical study subjects. In addition ...

Uw

Research Study Assistant

Seattle, WA · On-site

$21.70/hr

Reporting to David Horn, Associate Professor of Otolaryngology-Head and Neck Surgery, the Research Study Assistant supports clinical research by assisting with participant visits, data collection ...

previous page

Showing results 41-60

All JobsClinical Study JobsClinical Study Assistant Jobs

Clinical Study Assistant information

See salary details

$11

$20

$28

How much do clinical study assistant jobs pay per hour?

As of Aug 13, 2026, the average hourly pay for clinical study assistant in the United States is $20.23, according to ZipRecruiter salary data. Most workers in this role earn between $16.59 and $23.32 per hour, depending on experience, location, and employer.

What are the main challenges a clinical study assistant might face when supporting clinical trial operations?

A Clinical Study Assistant often encounters challenges such as managing multiple tasks under tight deadlines, ensuring accurate documentation, and coordinating communication between research teams, sponsors, and regulatory bodies. Additionally, adapting to evolving study protocols and maintaining compliance with strict regulatory requirements can be demanding. Strong organizational skills, attention to detail, and proactive communication are essential for navigating these challenges successfully.

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

AspectClinical Study AssistantClinical Research Coordinator
CredentialsTypically requires a bachelor's degree in health sciences or related fieldUsually requires a bachelor's degree, often with additional certifications in clinical research
Work EnvironmentSupports clinical trials in hospitals, research centers, or pharmaceutical companiesManages entire clinical studies, coordinating between sites, staff, and sponsors
Employer & IndustryHospitals, research institutions, pharmaceutical companiesAcademic medical centers, hospitals, research organizations
Search & Comparison IntentOften compared for entry-level roles supporting clinical trialsCompared for roles with broader responsibilities in clinical study management

The Clinical Study Assistant primarily supports clinical trial activities by assisting with data collection and documentation, while the Clinical Research Coordinator manages the overall conduct of the study, including patient recruitment and compliance. Both roles require similar educational backgrounds but differ in scope and responsibilities within the clinical research process.

What is a clinical study assistant?

Clinical Study Assistants are professionals who support the conduct of clinical trials by handling administrative tasks, maintaining study documentation, and ensuring regulatory compliance. They work closely with clinical research teams to coordinate schedules, communicate with study sites, and help manage trial materials. Their role is crucial in ensuring that clinical studies run smoothly, efficiently, and according to protocols and regulatory guidelines.

What are the key skills and qualifications needed to thrive as a clinical study assistant?

To thrive as a Clinical Study Assistant, you need strong organizational skills, attention to detail, and a background in life sciences or related fields, often supported by a bachelor's degree. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and regulatory documentation processes is typically required. Effective communication, teamwork, and problem-solving skills help you navigate complex study protocols and collaborate with diverse stakeholders. These abilities are crucial for ensuring the accuracy, compliance, and smooth operation of clinical research studies.
More about Clinical Study Assistant jobs
What cities are hiring for Clinical Study Assistant jobs? Cities with the most Clinical Study Assistant job openings:
What are the most commonly searched types of Clinical Study jobs? The most popular types of Clinical Study jobs are:
What states have the most Clinical Study Assistant jobs? States with the most job openings for Clinical Study Assistant jobs include:
Clinical Study Assistant jobs near you
Infographic showing various Clinical Study Assistant job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 72% Full Time, 17% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $42,079 per year, or $20.2 per hour.

Clinical Study Manager

Mobia Medical, Inc.

Fridley, MN • On-site

$110K - $160K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

This job post has expired today. Applications are no longer accepted.

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)

Apply