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Director Clinical Operations Jobs in Colorado (NOW HIRING)

Director, Clinical Applications

Denver, CO · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

As a trusted thought partner to clinical and operational leadership, the Director drives technology-enabled care transformation, leveraging AI, interoperability, and data-driven workflows to support ...

Clinical Director

Fort Collins, CO · On-site

$79K - $107K/yr

  • Medical

  • PTO

Exempt JOB SUMMARY The Clinical Director is responsible for the overall operation of the outpatient clinic, including daily management, ensuring that clinical supervision is available during all ...

Clinical Director

Denver, CO · On-site

$82K - $112K/yr

  • Medical

  • PTO

Exempt JOB SUMMARY The Clinical Director is responsible for the overall operation of the outpatient clinic, including daily management, ensuring that clinical supervision is available during all ...

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Showing results 1-20

Director Clinical Operations information

See Colorado salary details

$63.1K

$153.5K

$297.1K

How much do director clinical operations jobs pay per year?

As of Aug 13, 2026, the average yearly pay for director clinical operations in Colorado is $153,489.00, according to ZipRecruiter salary data. Most workers in this role earn between $107,300.00 and $182,400.00 per year, depending on experience, location, and employer.

What does a director of clinical operations do?

A director of clinical operations manages the daily operations of a healthcare facility or a specific department within a clinic or hospital. As a director of clinical operations, your responsibilities include scheduling staff to ensure proper coverage of patients and overseeing the productivity of your team to meet the organization's expectations. You define policies and procedures, facilitating further training when necessary. The director of clinical operations must also assess the performance of the medical team under your supervision regularly and mainstream processes when possible. Medical device manufacturers and pharmaceutical companies often hire a director of clinical operations to oversee research, lab, and testing operations.

What are the key skills and qualifications needed to thrive as a director of clinical operations?

To thrive as a Director of Clinical Operations, you need a robust background in clinical management, regulatory compliance, and healthcare administration, often supported by a relevant degree and substantial leadership experience. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and certifications like PMP or CCRA are commonly required. Exceptional leadership, strategic thinking, and communication skills help drive teams, manage stakeholders, and oversee complex projects. These skills are critical for ensuring clinical programs run efficiently, meet regulatory standards, and deliver high-quality patient outcomes.

What is the difference between Director Clinical Operations vs Clinical Project Manager?

AspectDirector Clinical OperationsClinical Project Manager
CredentialsTypically requires advanced degrees (e.g., MS, PhD) and extensive industry experienceUsually holds a bachelor's or master's degree in a related field, with relevant project management certifications
Work EnvironmentOversees multiple projects and teams across departments, strategic planningManages individual clinical trials, coordinates project activities, and timelines
Employer & Industry UsageUsed in pharmaceutical, biotech, and healthcare companies for senior leadership rolesCommonly employed in clinical research organizations and pharmaceutical companies for trial management

The main difference is that the Director Clinical Operations focuses on strategic oversight and leadership across multiple clinical trials, while the Clinical Project Manager handles the day-to-day management of specific clinical studies. Both roles require strong industry knowledge, but the director position involves broader responsibilities and higher-level decision-making.

What does a director of clinical operations do?

A Director of Clinical Operations is responsible for overseeing the day-to-day management and strategic direction of clinical trials and research activities within healthcare organizations or pharmaceutical companies. They ensure that clinical studies are conducted efficiently, ethically, and in compliance with regulatory requirements. This role involves supervising teams, managing budgets, developing protocols, and liaising with stakeholders to ensure successful trial outcomes. Directors of Clinical Operations play a crucial role in bringing new medical treatments to market by ensuring studies run smoothly from start to finish.

How does a director of clinical operations typically collaborate with cross-functional teams to ensure successful clinical trial execution?

A Director of Clinical Operations regularly collaborates with cross-functional teams such as regulatory affairs, data management, medical affairs, and biostatistics to ensure clinical trials are executed on time, within budget, and in compliance with regulations. This role involves leading team meetings, aligning project timelines, and facilitating communication between internal stakeholders and external partners like CROs and vendors. Strong coordination skills are essential, as the Director must balance diverse priorities and resolve any operational issues that arise, ensuring all teams work toward shared objectives.

What are the most commonly searched types of Clinical Operations jobs in Colorado?

The most popular types of Clinical Operations jobs in Colorado are:

What are popular job titles related to Director Clinical Operations jobs in Colorado?

For Director Clinical Operations jobs in Colorado, the most frequently searched job titles are:

What cities in Colorado are hiring for Director Clinical Operations jobs?

Cities in Colorado with the most Director Clinical Operations job openings:

Infographic showing various Director Clinical Operations job openings in Colorado as of August 2026, with employment types broken down into 85% Full Time, 12% Part Time, 1% Temporary, and 2% Contract. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $153,489 per year, or $73.8 per hour.

Director Clinical Research Operations

Cochlear Limited

Highlands Ranch, CO • On-site

$178 - $195/hr

Other

Medical, Dental, Vision, Life, Retirement, PTO

Posted 8 days ago


Job description

Director Clinical OperationsSkip to main content# CareersDirector Clinical Operations page is loaded## Director Clinical OperationsApplylocations: Lone Tree, Coloradotime type: Full timeposted on: Posted Yesterdaytime left to apply: End Date: August 1, 2026 (28 days left to apply)job requisition id: R-623700Change people’s lives and love what you do! Cochlear is the most recognized brand in hearing health care.**Director Clinical Operations****Position Spotlight:*** Lead regional clinical operations strategy and study execution for Cochlear Sponsored investigations* Oversee high-quality, compliant clinical research delivery across multiple countries and regulatory jurisdictions* Drive operational excellence, resource optimization, vendor strategy, site performance, and continuous improvement across the region* Serve as a senior clinical operations leader responsible for people leadership, budget accountability, inspection readiness, and regional stakeholder partnership* Hybrid work model of 3 days in office reporting to our North American headquarters in Lone Tree, CO* Willing to travel up to 20% regionally and internationally***About the role***Change people’s lives and love what you do at Cochlear—the most recognized brand in hearing health care—helping people hear and be heard around the world, while being part of one of Denver Business Journal’s 2026 Best Places to Work honorees in Denver. If you have experience leading clinical investigations and monitoring in the medical device/pharmaceutical industry and a passion for leadership, this is a fantastic opportunity to join the Clinical Operations team at the global leader in implantable hearing devices! In this role, you will be based in our Americas head office in Lone Tree, CO.The Director of Clinical Operations is responsible for developing and implementing the short- to medium-term clinical operations strategy for the region while managing the delivery of Cochlear Sponsored investigations. This role ensures clinical studies are delivered with regulatory excellence, operational efficiency, financial accountability, and alignment to business objectives and priorities.In this role, you will lead a team of Clinical Operations professionals, partner closely with regional stakeholders, sites, vendors, and cross-functional teams, and oversee the execution of complex, multi-site clinical investigations. You will be responsible for optimizing resources, strengthening operational capabilities, improving study delivery performance, managing regional vendor and site strategies, and using metrics and dashboards to drive continuous improvement in clinical research delivery.As a senior leader, you will also serve as a regional escalation point for complex operational challenges, support compliant study startup and site activation, oversee budgets and contracts, and help ensure readiness for audits, inspections, ethics committee interactions, and applicable regulatory requirements. This role requires deep clinical operations expertise, strong financial and analytical acumen, proven people leadership, and the ability to translate organizational strategy into effective regional execution.***Key Responsibilities**** Develop and implement the Clinical Operations strategy for study execution in the region, ensuring studies are executed on-time and within budget.* *Serve as the escalation point for complex operational challenges affecting the region, working collaboratively with Regional peers and team members to develop and implement solutions.** *Drive operational efficiency initiatives across regional clinical operations, identifying opportunities to standardize processes, leverage technology, optimize vendor relationships, and reduce waste.** *Direct clear performance expectations across the region to drive operational excellence and career growth.** *Ensure the Regional Clinical Operations team adheres to specific study protocols and complies with established regional and country-specific clinical research standards (including ISO 14155:2011 and 2020, ICH-GCP, MDR, IVDR, and applicable national regulations) governing the conduct of clinical studies.** *Serve as regional point of contact for regulatory inspections, audits, and ethics committee interactions****Key Requirements***To add value to Cochlear in this role you'll be able to meet and demonstrate the following knowledge, skills and abilities in your application and at interview:* Bachelor's Degree in Scientific or Health-related Discipline* 8-10 years' of progressive experience in clinical operations within the pharmaceutical or medical device industries, with at least 3 years in leadership roles* Proven experience managing clinical operations across multiple countries and regulatory jurisdictions* Deep knowledge of ISO 14155:2011 and 2020, ICH-GCP, and applicable regional regulations (e.g., FDA 21 CFR 812, MDR/IVDR, country-specific requirements across APAC)* Proven track record of planning and executing complex, multi-site, clinical investigations* Extensive experience with region-specific clinical research challenges (e.g., ethics committee processes, reimbursement landscapes, healthcare system structures)* Experience in people management and development, with demonstrated success building and leading high-performing teams* Demonstrated ability to translate organizational strategy and context into operational execution* Financial acumen including budget development, financial management, and resource optimisation* Proven ability to innovate, deliver change and navigate ambiguity* Understanding of quality systems, risk management, and regulatory compliance in the context of clinical research* Demonstrated ability to partner effectively with cross-functional stakeholders including Regulatory Affairs, Quality, Commercial, and external partners* Cultural intelligence and ability to work effectively across diverse organizational and cultural contexts* Strong analytical skills with ability to leverage data and metrics to drive decision-making and continuous improvement* Fluency in English; additional language skills highly valued* Willingness and ability to travel internationally (approximately 20%)**Total Rewards**In addition to the opportunity to develop your knowledge and grow professionally, we offer competitive wages and benefits.* Pay Range in the United States: $178,000 - $195,000 based upon experience, as well as an annual bonus opportunity of 20% of base salary. Exact compensation may vary based on skills, experience, and location.* Benefit package includes medical, dental, vision, life and disability insurance as well as 401(K) matching with immediate vesting, Paid Time Off, tuition reimbursement, maternity and paternity leave, Employee Stock Purchase Plan and pet insurance.***Who are we?***Human needs have always been our inspiration, ever since Professor Graeme Clark set out to create the first multi-channel cochlear implant because he saw his father struggle with hearing loss. We always start with people in mind – thinking about their needs.For this reason, our products, services and support will continue to evolve and improve. We are by our customers’ side through the entire hearing journey, so they can experience a life full of hearing. Our employees tell us that the number one reason they enjoy working for Cochlear is the opportunity to make a difference to people’s lives and working in an organization where they can be part of bringing the mission to life each day.***Physical & Mental Demands***The physical and mental demands described below are representative of those that must be met to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the individual is regularly required to be in a stationary (seated/standing) position; utilize business technology for work product delivery, communicate orally and in writing with others internal or external to the organization, utilize problem solving/critical thinking skills to discern and convey information. May be asked to occasionally transport/move up to 30 pounds, depending on the position. Specific vision abilities required by this job include ability to adjust focus. The individual is regularly required to utilize comprehension, critical thinking, communication, problem solving, organization reasoning, relating to others and discernment of items such as product specifications, procedures and processes to customers (whether internal or external). Influence, organization/classification of information and planning are also required.The work environment is a home/office. This is representative of the environment an individual may encounter while performing the essential functions of this job.***Apply now*** by completing your application form online. Applicants must meet the job specific application criteria to be considered. Visit our careers site at www.cochlear.us/careers to learn more.Cochlear Americas is an Equal Opportunity Employer. We will provide reasonable accommodations for qualified individuals with disabilities. If you require accommodation with completing the online application, please contact us via web or phone at 303-264-2549.*Application deadline: July 31, 2026* #J-18808-Ljbffr