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International Clinical Operations Jobs (NOW HIRING)

Jobgether

Opportunity to lead high-impact international clinical research and evidence development programs. * Broad strategic leadership role with visibility across global operations and client partnerships.

Gilead

Director, Clinical Operations

Parsippany, NJ · On-site

$210K - $272K/yr

Provides leadership and therapeutic expertise for the successful management of international clinical trials (Phase I - IV) across multiple indications through clinical study teams and through the ...

Gilead

Director, Clinical Operations

Foster City, CA · On-site

$210K - $272K/yr

Provides leadership and therapeutic expertise for the successful management of international clinical trials (Phase I - IV) across multiple indications through clinical study teams and through the ...

Gilead

Director, Clinical Operations

Parsippany, NJ · On-site

$210K - $272K/yr

Provides leadership and therapeutic expertise for the successful management of international clinical trials (Phase I - IV) across multiple indications through clinical study teams and through the ...

Gilead

Director, Clinical Operations

Foster City, CA · On-site

$210K - $272K/yr

Provides leadership and therapeutic expertise for the successful management of international clinical trials (Phase I - IV) across multiple indications through clinical study teams and through the ...

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International Clinical Operations information

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$35K

$98K

$186.5K

How much do international clinical operations jobs pay per year?

As of Jul 26, 2026, the average yearly pay for international 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 are International Clinical Operations?

International Clinical Operations refer to the planning, management, and execution of clinical trials conducted across multiple countries. Professionals in this field ensure that clinical studies comply with global regulatory standards, coordinate with international sites, and manage logistics such as patient recruitment, data collection, and reporting. Their work is essential for bringing new medical therapies to global markets efficiently and ethically. Successful international operations require strong project management skills, cultural awareness, and knowledge of local regulations. The ultimate goal is to ensure high-quality, timely, and compliant clinical trial outcomes worldwide.

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

To thrive in International Clinical Operations, you need a solid background in clinical research, regulatory compliance, project management, and typically a relevant life sciences degree. Familiarity with clinical trial management systems (CTMS), ICH-GCP guidelines, and certifications like ACRP or SOCRA are often required. Strong organizational, cross-cultural communication, and leadership skills help foster collaboration across global teams and sites. These skills ensure the efficient, compliant, and successful execution of multinational clinical trials.

What are some common challenges faced in International Clinical Operations, and how can professionals prepare for them?

Professionals in International Clinical Operations often encounter challenges such as navigating varying regulatory requirements across countries, managing communication across different time zones, and ensuring consistent protocol adherence at global sites. To prepare, it’s important to develop strong cross-cultural communication skills, stay updated on international regulatory guidelines, and utilize robust project management tools. Building a network of reliable local partners and being adaptable to changing environments also greatly contribute to overcoming these hurdles and ensuring successful trial execution.
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International Clinical Operations jobs near you
Infographic showing various International Clinical Operations job openings in the United States as of July 2026, with employment types broken down into 2% As Needed, 73% Full Time, 17% Part Time, and 8% 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.
Clinical Trials Manager - II

Clinical Trials Manager - II

Integrated Resources INC

Foster City, CA • On-site

Contractor

Posted 11 days ago

Job description

Job Description

Must meet all requirements for Principal Clinical Research Associate position and have demonstrated proficiency in all relevant areas. In partnership with CPMs, provides guidance and daily oversight for the successful management of all aspects of international clinical trials within designated program budgets and timelines. 

Coaches members of a work team and ensures adherence to established guidelines.

Provide input to program budget and timelines to ensure successful management of all aspects of international clinical trials. 

Anticipates obstacles and client difficulties and implements solutions to achieve project goals. 

Assists CPM in revising project timelines/budgets as necessary. Works with management on departmental issues, providing input to clinical operations strategies and work plans.

Communicates with functional peers regarding project status and issues and ensure project team goals are met. 

Contributes to development of abstracts, presentations and manuscripts.

Participate in the recruiting and hiring process for CPA/ CRAs and support their professional development.Participate in training of CPAs and CRAs. 

Provide guidance and training to CROs, vendors, investigators, and study coordinators on study requirements.
Excellent interpersonal skills and demonstrated ability to lead is required. Must be able to resolve problems using national and international regulations, guidelines, and investigator interaction. 

Strong communication and influence skills and ability to create a clear sense of direction is necessary. Must be able to resolve problems using national and international regulations, guidelines, and investigator interaction. 

Must have a demonstrated ability to successfully develop, implement, manage and complete clinical trials. Thorough knowledge and understanding of FDA and/or EMEA Regulations, ICH Guidelines, and GCPs governing the conduct of clinical trials is required. Experience in developing RFPs and selection and management of CROs/vendors. 

Ability to write study protocols, study reports, sections for investigator brochures, and regulatory documents (e.g. IND, NDA, etc.) with little supervision. 

Ability to examine functional issues from a broader organizational perspective. 

Functional expertise to initiate, author, or contribute to SOP development, implementation, and training.

Additional Information

All your information will be kept confidential according to EEO guidelines.

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About Integrated Resources

Sourced by ZipRecruiter

Integrated Resources Inc (IRI), based in Edison, NJ, US, is an esteemed player in the staffing solutions industry with a credible presence on their official website irionline.com. Notably, IRI provides a range of professional staffing services including contract, contract-to-hire, and direct hire solutions to a wide spectrum of industries such as healthcare, life sciences, manufacturing, financial, insurance, and others. Since its inception, IRI has been committed to delivering top-talent and optimum solutions to meet its clients' diverse needs.

Industry

Recruiting and staffing services

Company size

51 - 200 Employees

Headquarters location

Edison, NJ, US

Year founded

1996

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