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International Clinical Operations Jobs (NOW HIRING)

Orion Group

Clinical Operations Support

Orange, CA · On-site

$19 - $23.50/hr

Clinical Operations Support II - Skincare Location: Irvine, CA - 100% Onsite Contract Duration: 12 ... international recruitment companies. We have a network of 200 employees working from 24 offices ...

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 ...

Avant Staffing Professionals

NY · On-site

$80 - $100/hr

... with international clinicians, and fosters class-leading outcomes, ensuring Avant maintains a ... Operations. * 5 - 7 years of experience as a Registered Nurse * Minimum 2 years of leading people ...

11 Premier Research International LLC

NY · On-site

$110 - $130/hr

About Premier Research Premier Research is looking for a Manager, Clinical Operations to join our Clinical Monitoring, Site Management and SSU team. You will help biotech, medtech, and specialty ...

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How much do international clinical operations jobs pay per year?

As of Sep 5, 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 is 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?

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.

What does an international clinical operations person do?

An international clinical operations person manages and oversees clinical trials across multiple countries, ensuring compliance with local regulations and study protocols. They coordinate activities such as site selection, monitoring, data collection, and reporting, often using project management tools and requiring knowledge of Good Clinical Practice (GCP) standards.
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International Clinical Operations jobs near you
Infographic showing various International 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.

Head of Clinical Operations

Kumquat Biosciences Inc

San Diego, CA • On-site

$225K - $325K/yr

Full-time

Re-posted 23 days ago

Key responsibilities

  • Oversee the planning, execution, and delivery of clinical trial programs in collaboration with medical product leads.

  • Manage and support clinical operations teams, including study start-up, vendor oversight, and study progress monitoring.

  • Ensure compliance with regulatory guidelines and lead efforts for inspection readiness and audits.

Job description

Description:

We are looking for a highly experienced and results-driven Head of Clinical Operations to join our team at Kumquat Biosciences. As the Head of Clinical Operations, you will be responsible for overseeing the planning, execution, and delivery of clinical trial programs in collaboration with the medical product leads. This individual will oversee clinical operations across multiple studies and be responsible for operational excellence to meet corporate and clinical program goals. An ideal candidate is a strategic thinker with deep experience in clinical operations and cross-functional collaboration with excellent communication skills in the life sciences or healthcare industry.


Key Responsibilities:


  • Oversee the day-to-day clinical operations team, including Clinical Operations Study Leads (COSLs), Clinical Research Associates (CRAs), and other operations staff.
  • Develop and implement SOPs, work instructions, tools, templates, workflows, and study-level performance metrics to optimize operational efficiency and compliance.
  • Strike new and manage existing business relationships with CROs, clinical sites, vendors, and consultants to ensure high-quality vendor performance and financial accountability.
  • Collaborate with Medical, Clinical Science, Data Management, Quality Assurance, Regulatory, Clinical Supply, Regulatory and other departments to support clinical development programs.
  • Perform as a key member of a product development team to provide timelines, budgets, feasibility, and product strategy
  • Support COSLs in study start-up, development of study budgets, plans, and timely and quality study execution with excellent vendor oversight. 
  • Monitor clinical trial progress, identify risks and mitigation strategies, and provide regular updates to leadership.
  • Help strategize with study teams for rapid study start-up, site initiation, accruals to assigned product trials, and rapid database locks (60 days or less).
  • Ensure compliance with ICH-GCP guidelines, FDA regulations, and other applicable global regulatory requirements.
  • Lead and mentor team members, fostering a high-performance culture and supporting professional development.
  • Help lead inspection readiness initiative and regulatory authority inspections/audits. Be a key member of the audit response team. 


Requirements:
  • Bachelor's degree in a related field (Life Sciences, Nursing, etc.).
  • Minimum of 12 years of clinical research experience, including 5+ years in a leadership or management role.
  • Experience in early-phase oncology trials, and/or immunology and inflammation (I & I) trials, biomarker driven therapy, and small molecule drugs
  • Clinical operations lead of a minimum of 1 prior successful product approval and NDA submission with experience of a minimum of 1 accelerated approval pathway and compressed regulatory timelines
  • Experience in global clinical trials, early and late phase research
  • Strong understanding of clinical development processes, ICH-GCP, FDA, and international regulatory requirements.
  • Proven track record of successfully managing global clinical trials across all phases.
  • Excellent leadership, communication, and interpersonal skills.
  • Ability to thrive in a fast-paced, dynamic, and collaborative environment.