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Global Clinical Operations Jobs (NOW HIRING)

Philips

Director of Clinical Operations

Plymouth, MN · On-site

... FDA and global regulatory requirements, local country requirements, and Philips quality and ... Manage clinical operations governance, vendor oversight, and performance management across CROs ...

New

Philips

Director of Clinical Operations

Plymouth, MN

... FDA and global regulatory requirements, local country requirements, and Philips quality and ... Manage clinical operations governance, vendor oversight, and performance management across CROs ...

New

Philips

Director of Clinical Operations

Bothell, WA

... FDA and global regulatory requirements, local country requirements, and Philips quality and ... Manage clinical operations governance, vendor oversight, and performance management across CROs ...

New

Philips

Director of Clinical Operations

Bedford, MA

... FDA and global regulatory requirements, local country requirements, and Philips quality and ... Manage clinical operations governance, vendor oversight, and performance management across CROs ...

New

BeiGene, Inc.

Global Clinical Study Manager

... clinical operations and corporate goals and objectives • Experience in managing global oncology studies; preferably pivotal studies and inspection management with Hiring Authority. Essential ...

Iota Biosciences

Manager, Clinical Operations

Alameda, CA · On-site

$145K - $200K/yr

This role is ideal for someone who has experience in global Class III active implantable medical ... Manage a high performing clinical operations team by providing direction, subject matter expertise ...

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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.
Associate Director, Clinical Operations

Associate Director, Clinical Operations

Protagonist Therapeutics Inc.

Newark, CA • On-site

$185K - $205K/yr

Full-time

Re-posted 2 days ago

Job description

Associate Director, Clinical Operations
Skills & Attributes
Excellent organizational and leadership skills with very strong experience in executing Phase 1-3 global clinical trials. Experience leading a team managing international trials using CROs from set-up through to close out. Global clinical research expertise with excellent line and matrix management skills. Excellent teamwork, communication and interpersonal skills with a demonstrated ability to effectively develop talent. Highly developed critical thinking, prioritization and risk management skills to drive successful execution of trials. Strong knowledge of GCP and related international regulations. Excellent written and spoken English. Ability to work in a fast-paced dynamic environment.
Experience Required
5+ years global experience, with 5+ years at Senior Manager level or above in a Biotech/Pharma/CRO. Proven track record of effective leadership in a multi-disciplinary team.
Education Required
/Bachelor's Degree
Travel Required
Yes (up to 15%)
Job Summary
The Associate Director is accountable for the day-to-day management of the assigned clinical operations team. Provide strategic direction and leadership for the execution of trials. Accountable to ensure the delivery of appropriately skilled resources so that trials are delivered according to corporate objectives. Responsible for the delivery of clinical study milestones. Provide hands-on operations as necessary. Overseeing vendor activities with appropriate risk mitigations and contingency planning. Contribute strategic clinical operations input to the clinical development of Protagonist assets.
Core Responsibilities and skills
  • Primary operational leader of the clinical program implementation.
  • Participate in resource allocation, prioritization and budgeting to ensure department goals and milestones are aligned and tracking to corporate objectives. Line management responsibilities include hiring talent, performance development and mentorship.
  • Ensure ongoing strong vendor interactions and collaborations, including hands-on interactions and management.
  • Develop and manage integrated study timelines and leads study strategy meetings to review trial status/progress
  • Provide input on strategy in the development of realistic project milestones and deliverables. Apply appropriate project management tools and processes.
  • Lead ongoing risk assessments with accompanying mitigation plans and contingency plans. Strong abilities to problem-solve and diagnose the root causes and implement the appropriate corrective actions
  • Provide input to the development and review of study and overall clinical program budgets. Take corrective measures as necessary to keep project(s) in line within agreed timelines, quality, budget and performance metrics. Assess the impact of project scope changes to understand the implications on agreed plans and budgets.
  • Help develop site recruitment, enrollment and engagement strategies. Present overall scorecard and analysis to senior management.
  • Manage interdisciplinary activities to ensure clinical operations team collaborates effectively to set achievable goals, milestones and timelines. Establish strong cross-functional relationships and manage cross functional resources and study deliverables.
  • Identify and implement best practices and leverage lessons learnt and process improvements. Collaborate with Clinical Quality Assurance to develop a strategic plan for CRO and vendor audits. Proactively seek out, recommend and execute process improvements
  • Excellent oral and written communication skills with the ability to communicate clearly, succinctly and credibly to all organizational levels. A proven ability to anticipate and respond quickly to key emerging information.
  • Maintain oversight and contribute to the development of the department's standard operating procedures (SOPs). Ensure plans are developed in accordance with SOPs, and there is compliance with all controlled document requirements and other requirements to help guarantee quality deliverables.
  • Maintain knowledge of product areas, current trends, and literature to help ensure compliance
  • Drive excellence in the overall clinical operational activities across multiple clinical trials. Creative, dynamic and results-oriented. Act with integrity and respect at all times
  • Proficient in the use of computer and software systems (e.g., Excel, MS Project).
  • Perform other duties, initiatives and assignments as requested for the overall performance of the function and the company.

The base pay range for this position at commencement of employment is expected to be between $185K and $205K / year; however, base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience.
Protagonist Therapeutics is a discovery through late-stage development biopharmaceutical company. The Company's proprietary peptide technology platform enables de novo discovery of peptide therapeutics. Two novel peptides derived from Protagonist's proprietary discovery platform are at or near commercialization. ICOTYDE™ (icotrokinra) is approved in the U.S. for the treatment of moderate-to-severe plaque psoriasis in adults and pediatric patients 12 years of age and older who weigh at least 40 kg who are candidates for systemic therapy or phototherapy. ICOTYDE is the first and only targeted oral peptide that precisely blocks the Interleukin-23 receptor (IL-23R) licensed to Janssen Biotech, Inc.,a Johnson & Johnson company. ICOTYDE was jointly discovered by Protagonist and Johnson & Johnson scientists, with Protagonist having primary responsibility for the development of ICOTYDE through Phase 1, and Johnson & Johnson assuming responsibility for further development and commercialization. An NDA for rusfertide, a first-in-class hepcidin mimetic peptide that is being co-developed with Takeda Pharmaceuticals pursuant to a worldwide license and collaboration agreement entered in 2024, is under priority review with the FDA. Protagonist holds an option to co-commercialize rusfertide in the U.S. through a 50/50 profit and loss share structure or can opt-out of this structure. The Company also has a number of preclinical stage drug discovery programs addressing clinically and commercially validated targets including an oral IL-17 peptide antagonist, obesity dual and triple agonists, an oral hepcidin functional mimetic, and the recently announced IL-4 and amylin programs.
More information on Protagonist, its pipeline drug candidates, and clinical studies can be found on the Company's website at https://www.protagonist-inc.com.

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