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International Clinical Operations Jobs (NOW HIRING)

ExThera Medical

Clinical Operations Manager

Martinez, CA · On-site

A strategic and hands-on Clinical Operations Manager responsible for overseeing clinical trials for ... Ensure compliance of clinical trials with national and international regulatory requirements and co ...

IQVIA

Manager, Clinical Operations

Durham, NC

$86K - $216K/yr

... clinical operations management. May collaborate with other clinical teams and other functional ... International Conference on Harmonization (ICH) guidelines). Good leadership skills. Computer ...

Kite Pharma

Sr Clinical Trials Manager

Parsippany, NJ · On-site

$143K - $185K/yr

... international clinical trials. * Anticipates obstacles and client difficulties and implements ... Works with management on departmental issues, providing input to clinical operations strategies and ...

Kite Pharma

Sr Clinical Trials Manager

Santa Monica, CA · On-site

$143K - $185K/yr

... international clinical trials. * Anticipates obstacles and client difficulties and implements ... Works with management on departmental issues, providing input to clinical operations strategies and ...

Kite Pharma

Sr Clinical Trials Manager

Raleigh, NC · On-site

$143K - $185K/yr

... international clinical trials. * Anticipates obstacles and client difficulties and implements ... Works with management on departmental issues, providing input to clinical operations strategies and ...

IQVIA, Inc.

Manager, Clinical Operations

Durham, NC · On-site

$86K - $216K/yr

... by clinical operations management. • May collaborate with other clinical teams and other ... International Conference on Harmonization (ICH) guidelines). • Good leadership skills. • ...

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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 Jun 10, 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.
More about International Clinical Operations jobs
What job categories do people searching International Clinical Operations jobs look for? The top searched job categories for International Clinical Operations jobs are:
International Clinical Operations jobs near you
Infographic showing various International Clinical Operations job openings in the United States as of June 2026, with employment types broken down into 72% Full Time, 19% Part Time, and 9% Contract. Highlights an 95% Physical, 2% Hybrid, and 3% Remote job distribution, with an average salary of $98,039 per year, or $47.1 per hour.
Clinical Operations Manager

Clinical Operations Manager

ExThera Medical

Martinez, CA • On-site

Full-time

Posted 7 days ago

Job description

A strategic and hands-on Clinical Operations Manager responsible for overseeing clinical trials for medical devices while driving process remediation and operational excellence. This role requires a creative, resourceful, and flexible leader who can prioritize effectively, build structure where needed, and ensure clinical studies are conducted in full compliance with applicable regulatory standards.
Clinical Trial Leadership & Execution
  • Manage sponsor-led clinical trials for medical devices across the U.S. and EU.
  • Ensure all clinical studies are conducted in adherence to study protocols, ICH/GCP guidelines, and region specific regulations.
  • Direct protocol development and finalization in collaboration with cross-functional teams.
Process Improvement & TMF Remediation
  • Assess, remediate, and optimize clinical processes and work instructions to align with regulatory requirements, industry best practices, and organizational needs.
  • Assess Trial Master File(s) against applicable regulations and industry best practices.  As needed remediate structure of Trial Master File(s) and as applicable records to ensure audit readiness/ preparedness across studies.
Regulatory & Compliance Oversight
  • Serve as point of contact for IRB/EC submissions and correspondence (including central IRBs).
  • Oversee the creation and execution of clinical trial activities in accordance with Good Clinical Practices. Ensure compliance of clinical trials with national and international regulatory requirements and co-monitoring the assigned clinical trial following company SOPs.
  • Oversee preparation and submission of study-level regulatory documents
  • Contribute to validation plans and clinical performance study plans.
  • Perform periodic QC of the TMF

Site & Study Management
  • Proactive identification and management of study related risks
  • Responsible for developing and managing study related plans, processes including; Investigator agreements (CTA), CRFs, monitoring plan, data management, safety monitoring
  • Lead development and management of clinical trial documents including (but not limited to) protocols, Case Report Forms (CRFs), consent documents, confidentiality agreements.
  • Contribute to site identification, feasibility, and selection for clinical studies.
  • Oversee site initiation, monitoring, and close-out activities (SQV, SIV, IMV, COV) as required.
  • Develop and deliver training materials for internal teams, CROs, and study sites (e.g., protocols, device training, SIV presentations).
Leadership & Communication
  • Provide regular clinical program updates to executive leadership and project teams.
  • Foster a culture of accountability and continuous improvement.
  • All other duties as assigned
Qualifications
  • Bachelor’s degree or equivalent in life science
  • Minimum of 7+ years preferred of clinical project management experience in conducting clinical trials in sponsor medical device organization, preferably Class III devices
  • A solid understanding of the ICH guidelines/GCP
  • Experience interacting with regulators, including FDA
  • Ability to travel to visit clinical sites and for study meetings. Amount will vary upon project needs
  • Demonstrated ability to lead teams and work in a fast-paced team environment
  • Ability to successfully engage and work collaboratively with sites and internal teams
  • Excellent written and oral communication skills
     

 

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