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Sr Manager Clinical Operations Jobs (NOW HIRING)

You will have solid clinical operations experience, with the ability to manage competing priorities and develop your team. Required qualifications and experience: * Bachelor's degree in a relevant ...

Manager, Clinical Operations

Durham, NC · On-site

$86K - $216K/yr

... clinical operations management. • May collaborate with other clinical teams and other functional leadership to manage project related challenges and to achieve exemplary customer service. • ...

Manager, Clinical Operations

Durham, NC · On-site

$86K - $216K/yr

Ensures that staff are meeting defined workload and quality metrics through regular review and reporting of findings as outlined by clinical operations management. May collaborate with other clinical ...

The incumbent of this position will work closely with Best Care Best Experience, Quality Management, Communications, IS & T, Human Resources and Senior Leaders, Operational Directors and Managers, to ...

Ensures that staff are meeting defined workload and quality metrics through regular review and reporting of findings as outlined by clinical operations management. May collaborate with other clinical ...

Manager, Clinical Operations

Durham, NC · On-site

$86K - $216K/yr

Ensures that staff are meeting defined workload and quality metrics through regular review and reporting of findings as outlined by clinical operations management. May collaborate with other clinical ...

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Sr Manager Clinical Operations information

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$35K

$98K

$186.5K

How much do sr manager clinical operations jobs pay per year?

As of Sep 7, 2026, the average yearly pay for sr manager clinical operations 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 is a Sr Manager Clinical Operations?

A Sr Manager Clinical Operations is a senior professional responsible for overseeing the planning, execution, and management of clinical trials and studies within a healthcare or pharmaceutical organization. They ensure that clinical projects are conducted efficiently, comply with regulatory standards, and meet organizational goals. This role involves leading clinical operations teams, managing budgets and timelines, and collaborating with cross-functional departments. Sr Managers also play a key role in process improvement and maintaining high standards of data quality and patient safety.

What are the key skills and qualifications needed to thrive as a Sr Manager Clinical Operations, and why are they important?

To thrive as a Sr Manager Clinical Operations, you need a strong background in clinical research, project management, and regulatory compliance, typically supported by a degree in life sciences or a related field and extensive experience in clinical trials. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and GCP guidelines is essential, and certifications such as PMP or ACRP are often preferred. Exceptional leadership, strategic thinking, and communication skills help you effectively lead teams and manage complex projects. These capabilities are crucial for ensuring efficient trial execution, regulatory adherence, and the delivery of high-quality clinical outcomes.

What are some common challenges faced by a Sr Manager Clinical Operations, and how can they be addressed?

A Sr Manager Clinical Operations often encounters challenges such as coordinating cross-functional teams, ensuring regulatory compliance, and managing multiple clinical trial timelines simultaneously. Balancing the needs of various stakeholders—such as sponsors, investigators, and regulatory bodies—requires strong communication and leadership skills. Staying organized with robust project management tools and fostering transparent communication within the team can help address these challenges effectively. Additionally, proactively identifying potential risks and implementing mitigation strategies is key to maintaining smooth clinical trial operations.

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

AspectSr Manager Clinical OperationsClinical Project Manager
CredentialsTypically requires a Bachelor's or Master's in Life Sciences, with experience in clinical operationsRequires similar educational background, often with certifications like PMP
Work EnvironmentOversees multiple projects, manages teams, and ensures compliance across clinical trialsFocuses on managing individual clinical projects, timelines, and deliverables
Employer & Industry UsageCommon in pharmaceutical, biotech, and CRO companies for operational leadershipUsed in similar settings, often as a project-focused role within clinical research teams

The Sr Manager Clinical Operations typically has broader responsibilities overseeing multiple projects and teams, while the Clinical Project Manager concentrates on managing specific clinical trials. Both roles require similar credentials and are vital in clinical research, but differ in scope and focus.

More about Sr Manager Clinical Operations jobs

What cities are hiring for Sr Manager Clinical Operations jobs?

Cities with the most Sr Manager Clinical Operations job openings:

What states have the most Sr Manager Clinical Operations jobs?

States with the most job openings for Sr Manager Clinical Operations jobs include:

Infographic showing various Sr Manager Clinical Operations job openings in the United States as of August 2026, with employment types broken down into 84% Full Time, 13% Part Time, 1% Temporary, 1% Contract, and 1% Nights. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $98,039 per year, or $47.1 per hour.

Senior Manager, Clinical Operations - FSP Resource & Vendor Management

Biopharma Careers

King Of Prussia, PA • On-site

$170 - $201/hr

Other

Posted 4 days ago


Job description

The Senior Manager, Clinical Operations FSP Resource & Vendor Management

sits within the Clinical Operations organization and is accountable for the end‑to‑end oversight, planning, and optimization of FSP resources supporting Clinical Operations functions.

This role owns the Clinical Operations FSP workforce model, ensuring the right capabilities, capacity, and timing of resources to support portfolio delivery. The role serves as the primary Clinical Operations interface to FSP vendors and works in close partnership with the POE organization, which retains accountability for enterprise‑level contracting, sourcing strategy, and overall vendor governance.

Work Environment

*** This is a hybrid position based onsite at any of the posted locations with a minimum of 3 days onsite required weekly. Relocation and mobility assistance are not provided.

Main Responsibilities and AccountabilitiesClinical Operations FSP Workforce Ownership
  • Own the FSP resourcing strategy for Clinical Operations functions (e.g., study execution, site management, start‑up, monitoring, portfolio execution support).
  • Partner with Global and TA Clinical Operations leaders to understand portfolio plans, study mix, and anticipated demand across the study lifecycle.
  • Translate Clinical Operations demand into forward‑looking, data‑driven resourcing plans for FSP staff, including timing, skill mix, and capacity assumptions.
  • Continuously evolve and maintain resourcing algorithms and forecasting models to support proactive workforce planning.
FSP Vendor Relationship (Clinical Operations Scope)
  • Act as the primary Clinical Operations point of contact for assigned FSP vendors delivering ClinOps services.
  • Manage day‑to‑day operational relationships, including performance discussions, capacity planning, issue resolution, and continuous improvement.
  • Ensure FSP resources supporting Clinical Operations meet CSL expectations for quality, compliance, and delivery.
  • Escalate risks and performance issues through established governance channels, in alignment with POE frameworks.
Partnership with POE (Procurement / Outsourcing Excellence)
  • Work in close partnership with POE, who own enterprise‑level contracting, sourcing strategy, and vendor governance.
  • Provide Clinical Operations input into contracting strategies, SOW scope definitions, demand assumptions, and vendor performance discussions.
  • Ensure Clinical Operations resourcing needs are accurately reflected in POE‑led contracts and governance structures.
  • Align on roles and responsibilities to avoid duplication while ensuring strong operational ownership within Clinical Operations.
Financial Management & Invoicing (Clinical Operations FSP Spend)
  • Own financial oversight of Clinical Operations FSP labor spend, including forecasting, accruals, and variance management.
  • Review and approve FSP invoices related to Clinical Operations resources, ensuring accuracy, compliance, and alignment with delivered services.
  • Partner with Finance, Business Operations, and POE to ensure transparency and predictability of ClinOps FSP costs.
  • Support annual operating plans and long‑range forecasts related to FSP Clinical Operations capacity.
Systems, Data & Reporting
  • Ensure systems supporting Clinical Operations FSP tracking (resources, costs, utilization, performance) are accurate, current, and fit for purpose.
  • Drive standardization, resourcing algorithms and data quality across FSP resource and financial reporting.
  • Develop and maintain leadership‑ready dashboards and insights on capacity, cost, performance, and risk within Clinical Operations.
  • Identify opportunities to streamline processes and improve automation in partnership with POE and Business Operations.
Clinical Operations Enablement & Governance
  • Act as a trusted advisor to Clinical Operations leaders on FSP resourcing strategy, trade‑offs, and risk mitigation.
  • Provide clarity and guidance to study teams on FSP engagement models, resourcing processes, and financial expectations.
  • Support inspection readiness, audits, and internal reviews related to Clinical Operations vendor oversight and financial controls.
  • Contribute to the evolution of CSL’s Clinical Operations outsourcing model in line with transformation and operating‑model objectives.
Job Qualifications and Experience

Bachelor’s degree required; advanced degree preferred.

  • 8+ years of experience in Clinical Operations, outsourcing, vendor management, or business operations within pharma/biotech.
  • Demonstrated experience managing FSP or outsourced staff supporting Clinical Operations.
  • Strong understanding of clinical trial execution and Clinical Operations functional models.
  • Proven financial and analytical capability (forecasting, accruals, invoice review).
  • Experience partnering with procurement / outsourcing excellence organizations.
  • Comfortable operating in a complex, global, matrix environment.
Competencies
  • Strategic workforce planning
  • Vendor and stakeholder management
  • Financial and operational rigor
  • Data‑driven decision making
  • Clear, confident communication

The minimum and maximum base salary range that CSL expects to pay for this position at the Waltham, MA USA work location at the time of this posting is $170,000 - $201,000/yr. Individual base salary for a successful candidate is determined by qualifications, skill level, experience, competencies and other relevant factors. In addition to base salary, total compensation for this role may also include incentive compensation and equity.

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About CSL Behring

CSL Behring is a global biotherapeutics leader driven by our promise to save lives. Focused on serving patients’ needs by using the latest technologies, we discover, develop and deliver innovative therapies for people living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. We use three strategic scientific platforms of plasma fractionation, recombinant protein technology, and cell and gene therapy to support continued innovation and continually refine ways in which products can address unmet medical needs and help patients lead full lives.

CSL Behring operates one of the world’s largest plasma collection networks, CSL Plasma. Our parent company, CSL, headquartered in Melbourne, Australia, employs 32,000 people, and delivers its lifesaving therapies to people in more than 100 countries.

To learn more about CSL, CSL Behring, CSL Seqirus and CSL Vifor visit https://www.csl.com/ and CSL Plasma at https://www.cslplasma.com/ .

Our Benefits

For more information on CSL benefits visit How CSL Supports Your Well-being | CSL .

You Belong at CSL

At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future.

To learn more about inclusion and belonging visit https://www.csl.com/careers/inclusion-and-belonging

Equal Opportunity Employer

CSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please visit https://www.csl.com/accessibility-statement .

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