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Remote Senior Director Clinical Operations Jobs (NOW HIRING)

Senior Director, Clinical Operations

New York, NY · On-site +1

$225K - $265K/yr

About the Role As we continue to grow, we're seeking a Senior Director, Clinical Operations to lead ... With a strong remote culture, as well as offices in NYC and Princeton, we've been named one of the ...

Director, Clinical Operations Remote Company Overview: AMSURG is an independent leader in ... Provides timely and comprehensive updates to Clinical Quality Sr. Leadership regarding status of ...

Position Summary The Director, Clinical Operations is responsible for building and leading a ... Reports to: SVP, Clinical Affairs Location: Redwood City, CA (Hybrid) or Remote (USA) Primary ...

As the Director, Clinical Operations, you will lead the clinical operations function responsible ... ePRO, eTMF, and remote study platforms. * Oversee study startup and regulatory operations ...

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Remote Senior Director Clinical Operations information

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How much do remote senior director clinical operations jobs pay per year?

As of Jun 10, 2026, the average yearly pay for remote senior director clinical operations in the United States is $145,969.00, according to ZipRecruiter salary data. Most workers in this role earn between $102,000.00 and $173,500.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Remote Senior Director Clinical Operations, and why are they important?

To thrive as a Remote Senior Director Clinical Operations, you need extensive experience in clinical trial management, regulatory compliance, and leadership, usually backed by an advanced degree in life sciences or healthcare. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and relevant certifications like PMP or ACRP is highly valuable. Outstanding skills in strategic planning, communication, and cross-functional team leadership differentiate top performers in this role. These competencies ensure effective oversight of complex clinical programs, regulatory adherence, and successful collaboration across remote teams.

What does a Remote Senior Director of Clinical Operations do?

A Remote Senior Director of Clinical Operations oversees clinical trials and research operations, ensuring studies are conducted efficiently and in compliance with regulatory standards—all while working remotely. They lead cross-functional teams, manage budgets, develop operational strategies, and act as a liaison between internal teams and external partners. This leadership role requires a strong background in clinical research, excellent communication skills, and the ability to manage complex projects across multiple locations.

How does a Remote Senior Director Clinical Operations effectively manage and support geographically dispersed clinical teams?

As a Remote Senior Director Clinical Operations, you will leverage digital collaboration tools, regular virtual meetings, and clear communication protocols to oversee and support teams across multiple locations. Success in this role often involves establishing standardized processes, fostering a collaborative culture despite distance, and ensuring alignment with clinical trial objectives. You will also need to address challenges such as time zone differences and maintaining engagement, while providing leadership on trial execution, compliance, and quality metrics. Building strong relationships with cross-functional partners and implementing robust performance monitoring are essential for driving successful clinical operations remotely.

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

AspectRemote Senior Director Clinical OperationsClinical Project Manager
CredentialsAdvanced degrees (e.g., MD, PhD, or PharmD), extensive industry experienceBachelor's or Master's in life sciences, relevant project management certifications
Work EnvironmentStrategic leadership, overseeing multiple projects and teams remotelyManaging individual clinical trials, coordinating project activities
Employer & Industry UsagePharmaceutical companies, biotech firms, CROsPharmaceutical companies, CROs, clinical research organizations

The Remote Senior Director Clinical Operations focuses on strategic oversight and leadership of clinical programs at a high level, often managing teams remotely. In contrast, a Clinical Project Manager handles the day-to-day management of specific clinical trials, ensuring project milestones are met. Both roles require industry experience, but the senior director role involves broader oversight and strategic planning.

More about Remote Senior Director Clinical Operations jobs
What cities are hiring for Remote Senior Director Clinical Operations jobs? Cities with the most Remote Senior Director Clinical Operations job openings:
What states have the most Remote Senior Director Clinical Operations jobs? States with the most job openings for Remote Senior Director Clinical Operations jobs include:
Infographic showing various Remote Senior Director Clinical Operations job openings in the United States as of June 2026, with employment types broken down into 68% Full Time, 22% Part Time, and 10% Contract. Highlights an 87% Physical, 5% Hybrid, and 8% Remote job distribution, with an average salary of $145,969 per year, or $70.2 per hour.
Senior Director, Clinical Operations

Senior Director, Clinical Operations

Mitsubishi Tanabe Pharma America

Jersey City, NJ • On-site, Remote

Full-time

Medical, Dental, Life, Retirement, PTO

Posted 28 days ago


Job description

Company Description

Entrepreneurial
Spirit, Rooted in Tradition
. At Mitsubishi Tanabe Pharma Development America (MTDA), we can tout a storied reputation more than 300 years in the making. Our parent company, Mitsubishi Tanabe Pharma Corporation (MTPC), is a research-driven pharmaceutical company with global reach - and one of Japan's
oldest and most respected companies.
Relatively new to the U.S. market, the innovative compounds of the Mitsubishi Tanabe Pharma Group have already enjoyed commercial success under the brand labels of our U.S. partners. In this next phase of development, we plan to bring exciting new compounds to market under our own MT Pharma America label. We're currently building a new commercial organization and expanding our other functions to support this strategy.

Working with closely with the Head of Clinical Development and the Development Team Leader(s), the Senior Director, Clinical Operations directs global clinical operational activities for MTDA, guiding activities and influencing colleagues in a highly matrixed environment. Concurrently, the incumbent will also directly supervise a clinical operations staff and all activities related to executing clinical studies and full development programs in accordance with company SOPs, FDA, & ICH guidelines and regulations.

The Sr. Director, Clinical Operations will lead the operational strategy for trial execution, implementation, monitoring, analysis, data delivery and regulatory submission. He/she will lead the successful execution and timelines for clinical trials and programs drawing on a high level of expertise with clinical and regulatory requirements, both local and international, for clinical operational processes and requirements

Job Description

  • Lead overall operations program/team responsible for execution of global clinical program; oversee individuals managing operational execution of global clinical protocols for MTDA.

  • Provide clinical trial oversight and management, vendor and CRO performance (including bid/contract, budget/adjudication) and regulatory quality delivery of MTDA clinical trials according to corporate processes and timelines.

  • Participate in developing the long-range strategic plans for MTDA pipeline products and oversight of the clinical operations department.

  • Supervise internal and external staff associated with clinical operations as well as CROs and vendors associated with operational functions.

  • Recommend and/or assess potential CROs and vendors in collaboration with Sourcing and other colleagues.

  • Lead data review and discrepancy resolution, team meetings/presentations with senior management, in the US, EU and Japan, as needed.

  • Define and present complex operational objectives as required for senior management.

  • Oversee data collection activities for clinical programs: CRF, SAE assessment, queries, and follow-up, annual reports, investigator brochures, NDA etc.

  • Oversee management, professional development, training and performance of clinical operations staff/direct reports.



Qualifications
  • MS degree or equivalent.

  • Strong ability to build peer relationships and communicate effectively with company disciplines,
    cross-functional, and external teams.

  • 10+ years of increasing responsibility in clinical operations in a pharmaceutical company or CRO with a strong background in clinical trial design.

  • Deep expertise in outsourcing and CRO management; outstanding budget oversight and adjudication
    skills.

  • Successful experience in a large pharmaceutical company and complex matrix-based organization.

  • Proven history of drug R&D successes as evidenced in publications and regulatory success
    milestones (EOP2, NDA).

  • Experience in GI programs.

  • In-depth expertise in clinical and regulatory requirements, both local and international, of the clinical medicine and drug development processes.

  • Highly analytical, scientific mind with exceptional problem-solving skills.

  • Confident leader with proven ability to apply knowledge base to effectively manage, mentor and motivate staff to achieve corporate objectives.

  • Superior interpersonal skills coupled with multicultural awareness. Able to successfully establish relationships, communicate effectively within/across company disciplines and thrive within a global, highly matrixed organization.

  • Equally skilled at leading external teams at remote locations.

  • Well-honed project management skills; proven ability to simultaneously manage activities associated with multiple clinical trials and programs with short timelines in a fast-paced setting.

  • Attention to detail and commitment to high quality and on-time deliverables.

  • Outstanding computer skills including MS Office.

  • Willingness to travel up to 50% domestically and internationally.

Additional Information

Our Value Proposition:

Enjoy the fast-moving, entrepreneurial spirit more typically found in a small biotech, complemented by the benefits of a global pharmaceutical/chemical conglomerate. At this time, Mitsubishi Tanabe Pharma America offers our employees unparalleled opportunities for career success coupled with a supportive level of employee benefits:

Medical/Dental Life Insurance | Supplemental Life Insurance/Dependent Life Insurance |Accidental Death & Dismemberment Insurance | Business Travel Accident Insurance | Short-Term Disability | Long-Term Disability | Flexible Spending Accounts | Employee's Savings Plan (401K Plan) | Competitive Paid Time Off