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Non Clinical Study Operations Manager Jobs (NOW HIRING)

AbbVie

Study Project Manager II

Irvine, CA · On-site

$124K/yr

Leading the delivery of clinical operational strategies to ensure studies are executed with quality ... Experience in: drug, device, interventional and non-interventional, early feasibility studies

AbbVie

Study Project Manager II

Irvine, CA · On-site

Leading the delivery of clinical operational strategies to ensure studies are executed with quality ... Experience in: drug, device, interventional and non-interventional, early feasibility studies

Danaher

Senior Clinical Study Manager

The Senior Clinical Study Manager is responsible for clinical trial execution within the US and EU ... Provide strategic oversight into the operational planning and execution of complex programs and ...

Omni Inclusive

Spec 1, Clinical Operations

Irvine, CA · On-site

Ensure compliance with regulations and manage the lifecycle of devices, while closely partnering with other internal key stakeholders (e.g., clinical study teams, Manufacturing Operations, Finance ...

Zentalis

Sr Clinical Study Manager

San Diego, CA · Remote

... targeted, non-chemo, orally available medicine that enhances treatment experience, choice, and ... Clinical operations experience at a small or mid-size company. * Experience in running a trial from ...

ICON

Global Study Manager

Global Study Managers (GSMs) provide operational leadership across the full clinical study lifecycle, with accountability for the oversight and delivery of study management, site management, and ...

Icon plc

Global Study Managers (GSMs) provide operational leadership across the full clinical study lifecycle, with accountability for the oversight and delivery of study management, site management, and ...

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Non Clinical Study Operations Manager information

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How much do non clinical study operations manager jobs pay per year?

As of Sep 13, 2026, the average yearly pay for non clinical study operations manager in the United States is $98,039.00, according to ZipRecruiter salary data. Most workers in this role earn between $72,500.00 and $113,500.00 per year, depending on experience, location, and employer.

What does a non clinical study operations manager do?

A Non Clinical Study Operations Manager oversees the planning, execution, and management of non-clinical research studies, often in pharmaceutical or biotechnology settings. Their responsibilities include ensuring studies comply with regulatory requirements, managing budgets and timelines, coordinating with various teams, and maintaining documentation. They play a key role in supporting drug development by ensuring that preclinical studies, such as toxicology and pharmacology studies, run smoothly and efficiently. This role requires strong organizational, leadership, and communication skills, as well as a thorough understanding of Good Laboratory Practice (GLP) and other relevant guidelines.

What are the key skills and qualifications needed to thrive as a non clinical study operations manager?

To thrive as a Non Clinical Study Operations Manager, you need a background in life sciences, project management expertise, and experience with regulatory compliance, often supported by a relevant degree and industry certifications. Familiarity with Laboratory Information Management Systems (LIMS), data management tools, and Good Laboratory Practice (GLP) guidelines is typically required. Exceptional organizational, leadership, and communication skills help you coordinate cross-functional teams and manage complex study timelines. These competencies are crucial to ensure studies run efficiently, meet regulatory standards, and deliver reliable scientific results.

What are some common challenges faced by a non clinical study operations manager, and how can they be addressed?

A Non Clinical Study Operations Manager often encounters challenges such as coordinating complex study timelines, managing cross-functional teams, and ensuring regulatory compliance across diverse projects. To address these, it's important to maintain clear communication with stakeholders, implement robust project management tools, and stay updated on industry regulations. Building strong relationships with vendors and internal teams also helps anticipate and resolve potential bottlenecks efficiently.

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

AspectNon Clinical Study Operations ManagerClinical Research Coordinator
CredentialsBachelor's degree in life sciences, project management experienceBachelor's degree in health sciences or related field, clinical research certifications
Work EnvironmentLaboratories, research facilities, pharmaceutical companiesHospitals, clinics, research sites
Employer & IndustryPharmaceutical, biotech, contract research organizationsHospitals, academic medical centers, clinical trial sites

The Non Clinical Study Operations Manager primarily oversees preclinical research activities in labs and industry settings, focusing on study management and compliance. In contrast, the Clinical Research Coordinator manages clinical trial activities at research sites, ensuring patient recruitment and data collection. Both roles require related credentials and work within the broader clinical research industry, but they differ in focus and environment.

What are popular job titles related to Non Clinical Study Operations Manager jobs?

For Non Clinical Study Operations Manager jobs, the most frequently searched job titles are:

Infographic showing various Non Clinical Study Operations Manager job openings in the United States as of September 2026, with employment types broken down into 94% Full Time, and 6% Part Time. Highlights an 83% In-person, and 17% Remote job distribution, with an average salary of $98,039 per year, or $47.1 per hour.

Clinical Study Operations Manager

Boston, MA • On-site, Remote

Beacon Biosignals
Software Development • 1 - 10 employees
Learn more about Beacon Biosignalsexternal

$90K - $110K/yr

Full-time, Contractor

PTO

Re-posted 14 days ago

Job description

As a Clinical Study Operations Manager within the Clinical Study Operations team, you will be responsible for ensuring the successful operational delivery of Beacon's clinical studies, from startup through close-out. You will work closely with sponsors, project teams, and clinical sites to drive efficient study execution and uphold Beacon's commitment to quality, compliance, and scientific rigor.
 
You will oversee study startup planning, site onboarding and training, and ongoing operational oversight to ensure studies are executed on time and to the highest standards. Acting as a key operational partner to both sponsors and internal teams, you will proactively identify risks, streamline communication, and maintain alignment across stakeholders. In addition, you will foster a culture of quality within the organization by coaching peers on GCP compliance, documentation discipline, version control, and complaint management, strengthening the team's collective operational excellence.
 
This is a contract-to-hire individual contributor role, fully remote anywhere in the U.S., and will require up to 10% travel. Beacon's robust asynchronous work practices ensure a first-class remote work experience, but we also have in-person office hubs available located in Boston, New York and Paris.
 
What success looks like:
  • Collaborate with project teams to implement study startup activities, including communication planning, logistics, development of study documentation, and data configuration.
  • Instill confidence with clients on study operations through start up, maintenance and close out activities.
  • Act as the primary point of contact for clinical sites, ensuring smooth operations and clear communication.
  • Provide training to research sites on the use of Beacon's devices and study protocols, ensuring proper device usage and data collection.
  • Monitor project progress, ensuring adherence to timelines, protocols, and quality standards.
  • Maintain compliance with Good Clinical Practice (GCP), International Conference on Harmonization (ICH) guidelines, and regulatory standards.
  • Foster a culture of quality within the ClinOps and Scientific teams by coaching peers on GCP requirements, documentation discipline, versioning, and complaint management.
  • Address operational issues promptly, escalating through tools like Zendesk and Asana for resolution.
  • Provide actionable feedback from research sites to inform improvements in devices and workflows.
 
What you will bring:
  • 5+ years of experience in clinical project management or clinical operations roles.
  • Strong organizational and project management skills, with the ability to manage multiple responsibilities effectively.
  • Excellent written and verbal communication skills in English; additional languages are a bonus.
  • A proactive mindset with the ability to identify priorities and anticipate challenges.
  • Meticulous attention to detail, ensuring accuracy in data collection and reporting.
  • Ability to work in a fast paced environment with multiple priorities.
  • Familiarity with GCP, ICH guidelines, and clinical research regulatory requirements.
  • Knowledge of decentralized data collection, compliance and oversight while showing empathy for both patients and sites.
  • A desire to learn more about analytics, statistics, machine learning, and clinical trials.
The salary range for this role is $90,000 - $110,000. Salary ranges are determined using current market compensation data for this role and adjusted based on experience, skills, and location. The base salary is one component of the total compensation package, which includes equity, PTO and other benefits.
 
At Beacon, we've found that cultural and scientific impact is driven most by those that lead by example. As such, we're always seeking new contributors whose work demonstrates an avid curiosity, a bias towards simplicity, an eye for composability, a self-service mindset, and - most of all - a deep empathy towards colleagues, stakeholders, users, and patients. We believe a diverse team builds more robust systems and achieves higher impact.

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