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Global Clinical Operations Jobs (NOW HIRING)

Verastem

Associate Director Clinical Supply

Needham, MA · On-site

$175K - $200K/yr

The Associate Director also serves as the operational backup to the Director of Global Clinical Supply as needed Responsibilities: * Develop and execute global clinical supply strategies for multiple ...

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Verastem

Associate Director Clinical Supply

Needham, MA · On-site

$175K - $200K/yr

The Associate Director also serves as the operational backup to the Director of Global Clinical Supply as needed Responsibilities: * Develop and execute global clinical supply strategies for multiple ...

New

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Global Clinical Operations information

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$35K

$98K

$186.5K

How much do global clinical operations jobs pay per year?

As of Jul 17, 2026, the average yearly pay for global 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 does a clinical operations person do?

A clinical operations person manages the planning, execution, and oversight of clinical trials to ensure they are completed on time, within budget, and in compliance with regulations. They coordinate activities such as site selection, patient recruitment, data collection, and vendor management, often using tools like clinical trial management systems (CTMS).

Can I get paid to participate in trials?

In clinical research, participants are often compensated for their time and effort, especially in clinical trials conducted by professionals in global clinical operations. Payment varies depending on the study's complexity, duration, and location, and participants may need to meet specific health or eligibility criteria. Compensation is typically provided in the form of cash, gift cards, or other incentives, and adherence to study protocols is essential for eligibility.

What is global clinical operations?

Global clinical operations is a department within the pharmaceutical or biotech industry responsible for managing and coordinating clinical trials across multiple countries. It involves planning, execution, and oversight of trial activities, ensuring compliance with regulatory requirements, and managing cross-border teams and vendors. Professionals in this field often use project management skills and regulatory knowledge to ensure trials are completed efficiently and accurately.

How do Global Clinical Operations teams typically collaborate with cross-functional stakeholders during a clinical trial?

Global Clinical Operations professionals regularly work with multidisciplinary teams, including regulatory affairs, data management, medical writing, and site management. Effective collaboration is essential to coordinate timelines, ensure protocol compliance, and address site or patient issues as they arise. Team members often participate in regular cross-functional meetings and use project management tools to track progress and share updates. Building strong communication skills and understanding each stakeholder's role are crucial for success in this collaborative environment.

Who is the biggest CRO in the world?

In the context of global clinical operations, the largest Contract Research Organization (CRO) worldwide is IQVIA, which provides comprehensive services for clinical trials, data management, and regulatory consulting. It operates across multiple regions and employs advanced technology and skilled professionals to support pharmaceutical and biotech companies in drug development.

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

AspectGlobal Clinical OperationsClinical Project Manager
ResponsibilitiesOversees multiple clinical trials across regions, manages global teams, and ensures compliance with international regulations.Manages individual clinical trials, coordinates project activities, and ensures milestones are met within a specific project.
Required CredentialsTypically requires a degree in life sciences, clinical research experience, and often advanced certifications.Requires a degree in life sciences or related field, with experience in clinical trial management.
Work EnvironmentGlobal offices, international sites, cross-cultural teams.Clinical sites, project teams, and local offices.

Global Clinical Operations focus on managing multiple trials worldwide, overseeing teams and compliance across regions. Clinical Project Managers handle specific trials, coordinating activities to meet project goals. Both roles require similar credentials but differ in scope and scale.

What are the key skills and qualifications needed to thrive in Global Clinical Operations, and why are they important?

To thrive in Global Clinical Operations, you need expertise in clinical trial management, regulatory knowledge, and a background in life sciences or a related field, often supported by advanced degrees or certifications like PMP or ACRP. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and global regulatory platforms is crucial. Strong leadership, cross-cultural communication, and problem-solving abilities help manage diverse teams and complex projects across regions. These skills ensure successful, compliant execution of global studies and drive efficient delivery of high-quality clinical data.
More about Global Clinical Operations jobs
What states have the most Global Clinical Operations jobs? States with the most job openings for Global Clinical Operations jobs include:
What job categories do people searching Global Clinical Operations jobs look for? The top searched job categories for Global Clinical Operations jobs are:
Global Clinical Operations jobs near you
Infographic showing various Global Clinical Operations job openings in the United States as of July 2026, with employment types broken down into 3% As Needed, 72% Full Time, 18% Part Time, and 7% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $98,039 per year, or $47.1 per hour.
Senior Director, Clinical Operations

Senior Director, Clinical Operations

Janux Therapeutics

San Diego, CA • On-site, Remote

$245K - $260K/yr

Full-time

Re-posted 11 days ago

Job description

The Senior Director of Clinical Operations will provide global operational leadership overseeing complex clinical programs focusing on innovative T-cell engager therapies for immunology and oncology indications. This role is responsible for efficient planning, resourcing and execution of portfolio level programs in adherence to ICH-GCP, FDA regulations, and company SOPs. The Senior Director will report into the Vice President, Clinical Operations and will ensure strategic alignment of programs and key stakeholder management in a fast-paced environment, while mentoring and growing the Clinical Operations team and culture to ensure successful program delivery.
ESSENTIAL FUNCTIONS AND RESPONSIBILITIES
  • Drive global clinical operations strategy and execution for programs ensuring all clinical activities support IND-enabling -Phase 3 objectives, as well as future clinical development plans.
  • Collaborate effectively cross-functionally with senior leadership to ensure operational initiatives support strategic company goals.
  • Establish and refine scalable best practices to drive efficiency while preparing for future departmental growth.
  • Oversee the development, review, and operational implementation of study documents, including protocols, informed consent forms, CRFs, monitoring plans, and pharmacy manuals ensuring consistency among programs.
  • Responsible for successful external partner relationships including CROs, central labs, patient advocacy groups and others. Ensure deliverables are met on time, within budget, and to quality standards.
  • Prepare and deliver program updates, establish KPIs and dashboards, and effectively present to all study teams.  Strongly represent Clinical Operations in internal and external meetings.
  • Mentor and support direct reports, fostering professional development, team performance and a strong culture.
  • Oversee site strategy and establish Clinical Operations team relationships with investigators and key opinion leaders.
  • Contribute to the development and implementation of SOPs, work instructions, and operational plans to enhance team efficiency and compliance.
  • Develop and implement operational plans, timelines, and budgets for clinical programs.
  • Ensure all trial activities are conducted in accordance with the protocol, SOPs, GCP, and applicable regulations.
REQUIRED EDUCATION, EXPERIENCE, SKILLS, AND ABILITIES
  • Bachelor’s degree in life sciences or related field with 12+ years of experience in clinical research, including at least 10 years in clinical trial management. Advanced degree preferred.
  • Strong experience in complex autoimmune indications, early phase experience strongly preferred.
  • Ability to define strategy and ensure organizational goals are executed in global clinical operations plans.
  • Proven track record of leading complex clinical programs from start to completion.
  • Strong knowledge of ICH GCP, FDA regulations, and global clinical regulatory guidelines.
  • Strong IT skills in MS Office and clinical trial systems (e.g., CTMS, eTMF, EDC).
  • Expertise in clinical budgeting and efficient allocation of resources
  • Demonstrated success in leading, mentoring, developing diverse clinical teams and providing oversight to CROs.
  • Excellent communication, leadership, and interpersonal skills, including the ability to understand and present technical information effectively to executive leadership.
  • Strong organizational and time management abilities.
  • High level of accountability, adaptability, and attention to detail with an ability to set priorities and handle multiple tasks simultaneously in a changing environment.
  • Ability to work independently and collaboratively in a fast-paced, matrixed environment.
In addition to a competitive base salary ranging from $245,000 to $260,000, we offer stock options, restricted stock units, a stock purchase plan (ESPP) and a target bonus.  Janux also provides a comprehensive benefits package for our employees and their families, which includes medical, dental, vision, and supplemental disability insurance. Relocation assistance may also be available.
Please note that the hourly rate range is a guideline, and individual total compensation will vary based on factors such as qualifications, skill level, competencies, and internal equity.
Job Type: Full-time
Benefits:
·             Annual bonus program
·             Incentive stock option plan
·             401k plan with flat non-elective employer contribution
·             Comprehensive medical insurance with 90-100% employer-paid premiums
·             Dental and vision insurance
·             HSA, FSA, and supplemental insurance plans (life, disability, accident, critical illness, hospital indemnity)
·             Unlimited PTO
·             Generous holiday schedule; includes summer and winter company shutdown
·             Relocation assistance
Schedule:
·             Monday to Friday
Work authorization:
·             United States (Required)
Additional Compensation:
·             Annual targeted bonus %
Work Location:
·             Hybrid preferred in San Diego office. Remote permitted upon approval, with ability to travel up to 25% for meetings or site visits as required.
 
EQUAL OPPORTUNITY EMPLOYER:
Janux Therapeutics, Inc. is an equal opportunity employer that is committed to providing a work environment free of harassment and discrimination based upon a protected category, as well as an environment free from retaliation for protected activity.

We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.