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Temporary Clinical Trial Operations Jobs (NOW HIRING)

IQVIA

Clinical Trial Operations Specialist

Durham, NC · Remote

$68K - $171K/yr

Job Posting Title- Clinical Trial Operations Specialist (CTOS) Location: Home-based in the U.S. Job Overview Provide operational support and coordination for global clinical trials, ensuring ...

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IQVIA

Clinical Trial Operations Specialist

Durham, NC · Remote

$68K - $171K/yr

Job Posting Title- Clinical Trial Operations Specialist (CTOS) Location: Home-based in the U.S. Job Overview Provide operational support and coordination for global clinical trials, ensuring ...

New

Icon plc

Senior Clinical Trial Associate

Blue Bell, PA

$32 - $43.75/hr

Senior Clinical Trial Associate ICON is a global healthcare intelligence and clinical research ... Collaborating with cross-functional teams to support trial operations and resolve any issues that ...

ICON

Senior Clinical Trial Associate

Blue Bell, PA · On-site +1

$32 - $43.75/hr

Senior Clinical Trial Associate ICON is a global healthcare intelligence and clinical research ... Collaborating with cross-functional teams to support trial operations and resolve any issues that ...

Kardigan

Clinical Trial Manager

Princeton, NJ · Remote

As a Clinical Trial Manager (CTM), you will be part of the Clinical Operations team reporting to the asset's Clinical Trial or Clinical Program Lead. This position will be responsible for the ...

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How much do temporary clinical trial operations jobs pay per hour?

As of Jul 14, 2026, the average hourly pay for temporary clinical trial operations in the United States is $39.99, according to ZipRecruiter salary data. Most workers in this role earn between $32.21 and $43.99 per hour, depending on experience, location, and employer.

What jobs pay $10,000 a week?

In the field of temporary clinical trial operations, high weekly earnings of $10,000 or more are uncommon and typically associated with senior-level roles, project managers, or consultants with extensive experience and specialized skills. Such compensation may also be found in executive or highly specialized positions within the healthcare or pharmaceutical industries, often requiring advanced certifications and a strong track record. Most roles in clinical trial operations offer salaries below this level, but top-tier consultants or those working on large, complex trials may reach or exceed this threshold.

What jobs make $3,000 a day?

In the field of temporary clinical trial operations, high-paying roles such as senior clinical trial managers or principal investigators can earn around $3,000 per day, especially when overseeing large or complex studies. These positions typically require extensive experience, specialized knowledge, and often involve contract or consulting work with flexible schedules. Compensation varies based on project scope, location, and individual expertise.

Is CRA better than CRC?

A Clinical Research Associate (CRA) typically oversees multiple clinical trials, monitors site compliance, and ensures data quality, often requiring travel and certification such as CCRP. A Clinical Research Coordinator (CRC) manages daily trial activities at a specific site, handles patient interactions, and maintains study documentation. Both roles are essential, but CRAs usually have more responsibility for oversight and may require more experience or advanced training.

Why do 90% of clinical trials fail?

Clinical trial operations professionals understand that about 90% of trials fail due to issues like patient recruitment challenges, protocol deviations, or insufficient data quality. Effective planning, clear communication, and adherence to regulatory standards are essential to improve trial success rates.

What is the difference between Temporary Clinical Trial Operations vs Clinical Trial Coordinators?

AspectTemporary Clinical Trial OperationsClinical Trial Coordinators
CredentialsRelevant experience, sometimes certifications in clinical researchOften require a degree in health sciences or related field, plus certification
Work EnvironmentContract-based, project-specific settings within research organizationsTypically office-based, coordinating daily trial activities
Employer & Industry UsageUsed by CROs, pharmaceutical companies for short-term needsCommonly employed by research sites and hospitals

Temporary Clinical Trial Operations roles focus on short-term, project-specific tasks within clinical research, often requiring specialized experience or certifications. Clinical Trial Coordinators handle ongoing trial management and participant coordination, usually with a background in health sciences. Both roles are essential in the clinical research process but differ mainly in duration, scope, and employment setting.

More about Temporary Clinical Trial Operations jobs
What cities are hiring for Temporary Clinical Trial Operations jobs? Cities with the most Temporary Clinical Trial Operations job openings:
What are the most commonly searched types of Clinical Trial Operations jobs? The most popular types of Clinical Trial Operations jobs are:
What states have the most Temporary Clinical Trial Operations jobs? States with the most job openings for Temporary Clinical Trial Operations jobs include:
What job categories do people searching Temporary Clinical Trial Operations jobs look for? The top searched job categories for Temporary Clinical Trial Operations jobs are:
Temporary Clinical Trial Operations jobs near you
Infographic showing various Temporary Clinical Trial 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 $83,169 per year, or $40 per hour.
Clinical Trial Operations Specialist

Clinical Trial Operations Specialist

IQVIA

Durham, NC • Remote

$68K - $171K/yr

Full-time

This job post has expired today. Applications are no longer accepted.

IQVIA rating

8.1

Company rating: 8.1 out of 10

Based on 53 frontline employees who took The Breakroom Quiz

56th of 210 rated it services

Job description

Job Posting Title- Clinical Trial Operations Specialist (CTOS) Location: Home-based in the U.S. Job Overview

Provide operational support and coordination for global clinical trials, ensuring efficient trial execution from planning through close-out. Responsible for managing trial-related documentation, systems, communication, and logistics in compliance with SOPs, ICH-GCP, and regulatory requirements, while meeting quality and timeline objectives.

Essential Functions
  • Plan, coordinate, and execute clinical trial activities across regions in compliance with ICH-GCP, ensuring timely and high-quality delivery.
  • Maintain and oversee trial documentation (e.g., ISF, TMF, submissions), ensuring completeness, accuracy, timeliness and audit readiness.
  • Collaborate with global and regional stakeholders, vendors, and trial teams to ensure seamless trial conduct and communication.
  • Manage and maintain clinical trial systems, databases, and tracking tools ensuring data accuracy.
  • Prepare and distribute project plans, status updates, reports, and presentation materials.
  • Monitor trial progress, budgets, and system data, identifying risks and implementing corrective actions as needed.
  • Coordinate documentation workflows, regulatory submissions, and communication with authorities and regional teams.
  • Support reporting, trial close-out activities, and preparation of key deliverables (e.g., CTR appendices).
  • Coordinate logistics for trial meetings, materials, and supplies.
  • Contribute to quality oversight, inspection readiness, and best practices in clinical trial conduct.
  • Act as a key point of contact for trial-related systems, documentation, and operational queries.
Qualifications
  • University degree qualified and/or comparable professional education with at least 3+ years' experience in clinical trial operations or project coordination.
  • Exceptional communication and stakeholder management skills.
  • Strong knowledge of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
  • Excellent organizational and problem-solving skills with ability to work independently, prioritize tasks, and manage projects in a complex international environment.
  • Detail-oriented with strong commitment to quality and compliance.
  • Proficiency in MS Office and clinical trial systems/tools.
  • Fluent in written and spoken English.

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IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more athttps://jobs.iqvia.com

IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

The potential base pay range for this role, when annualized, is $68,400.00 - $171,000.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

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About IQVIA

Sourced by ZipRecruiter

At IQVIA, we are passionate about helping customers and partners improve results and patient outcomes. Everything we do contributes to this vision for creating a healthier world. In today’s healthcare environment, it’s not only about how much data, information, and technology you have at your fingertips – it’s what you do with it. IQVIA is focused on making intelligent connections for customers across the entire healthcare ecosystem to help you drive healthcare forward. Whether that means partnering with novel technology companies to boost patient engagement, leveraging AI & machine learning to accelerate results, or using decentralized trials to reach the right patients wherever they are – we are always looking for smarter ways to move you forward.

Industry

Health care and social assistance

Company size

10,000+ Employees

Headquarters location

Durham, NC, US

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