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Temporary Clinical Trial Operations Jobs in Raleigh, NC

Remote (United States) Employment Type: Full-Time Our client is seeking a Budget Operations Specialist to support global clinical trial operations by managing investigator budgets, site setup, and ...

As a Clinical Trial Manager at ICON, you will manage clinical trial operations activities, supporting your team and stakeholders to deliver high-quality outcomes across our clinical programmes. What ...

As a Clinical Trial Manager at ICON, you will manage clinical trial operations activities, supporting your team and stakeholders to deliver high-quality outcomes across our clinical programmes. What ...

As a Clinical Trial Manager at ICON, you will manage clinical trial operations activities, supporting your team and stakeholders to deliver high-quality outcomes across our clinical programmes. What ...

Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations. Your Profile: You will have a strong foundation in clinical trial ...

As a Clinical Trial Manager at ICON, you will manage clinical trial operations activities, supporting your team and stakeholders to deliver high-quality outcomes across our clinical programmes. What ...

You will oversee local trial operations, drive performance, and collaborate cross-functionally to ... This role is ideal for a clinical operations professional who thrives in a fast-paced, large ...

You will oversee local trial operations, drive performance, and collaborate cross-functionally to ... This role is ideal for a clinical operations professional who thrives in a fast-paced, large ...

Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations. Your Profile: You will have a strong foundation in clinical trial ...

Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations. Your Profile: You will have a strong foundation in clinical trial ...

Strong knowledge of clinical trial operations, study start-up, maintenance, and close-out activities. * Strong knowledge of ICH/GCP guidelines, applicable regulatory requirements, clinical study ...

Strong knowledge of clinical trial operations, study start-up, maintenance, and close-out activities. * Strong knowledge of ICH/GCP guidelines, applicable regulatory requirements, clinical study ...

Strong knowledge of clinical trial operations, study start-up, maintenance, and close-out activities. * Strong knowledge of ICH/GCP guidelines, applicable regulatory requirements, clinical study ...

Strong knowledge of clinical trial operations, study start-up, maintenance, and close-out activities. * Strong knowledge of ICH/GCP guidelines, applicable regulatory requirements, clinical study ...

Showing results 21-40

Temporary Clinical Trial Operations information

See Raleigh, NC salary details

$16

$38

$68

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

As of Aug 16, 2026, the average hourly pay for temporary clinical trial operations in Raleigh, NC is $38.87, according to ZipRecruiter salary data. Most workers in this role earn between $31.30 and $42.74 per hour, depending on experience, location, and employer.

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.

What are the most commonly searched types of Clinical Trial Operations jobs in Raleigh, NC?

The most popular types of Clinical Trial Operations jobs in Raleigh, NC are:

What are popular job titles related to Temporary Clinical Trial Operations jobs in Raleigh, NC?

For Temporary Clinical Trial Operations jobs in Raleigh, NC, the most frequently searched job titles are:

What job categories do people searching Temporary Clinical Trial Operations jobs in Raleigh, NC look for?

The top searched job categories for Temporary Clinical Trial Operations jobs in Raleigh, NC are:

What cities near Raleigh, NC are hiring for Temporary Clinical Trial Operations jobs?

Cities near Raleigh, NC with the most Temporary Clinical Trial Operations job openings:

Patient Site Engagement Operations Specialist

IQVIA, Inc.

Durham, NC • On-site

$62K - $157K/yr

Full-time

Re-posted 25 days ago


IQVIA rating

8.1

Company rating: 8.1 out of 10

Based on 53 frontline employees who took The Breakroom Quiz

62nd of 224 rated it services


Job description

Overview:
Patient & Site Engagement (PSE) Operations Specialist (OS) services provide the PSE Managers with administrative support for the management, execution and timely delivery of tactics for patient and site-facing initiatives in support of a clinical trial. Interface with key Delivery Unit customers Trial Delivery Leaders (TDLs), Trial Delivery Managers (TDMs). Interface with key Global Clinical Operations (GCO) customers Local Trial Manager (LTM) and Site Manager (SM), suppliers, and other stakeholders involved in the development, management, and dissemination of patient and site-facing tactics.
Responsibilities:
  • Services rendered will adhere to applicable sponsor SOPs, WIs, policies, local regulatory requirements, etc.
  • Comply with relevant time reporting systems, training requirements and developing therapeutic knowledge enough for role and responsibilities.
  • Ensure accuracy and oversight of Scope of Work (SOW) to reflect all External Service Providers planned services and budgets. This includes forecasting and proactive management of PSE trial budgets and Purchase Orders.
  • Keep the project plan updated in relation to timelines and budget based on the scope of work for delivery of the tools and tactics for a clinical trial.
  • Drive execution of tactics and initiatives through management of service providers as required by business including: creative and content development, global translations, material production, technical development of apps, websites, and other technological tools to promote patient/caregiver and/or site engagement.
  • Ensure compliance with sponsor policies by way of documenting Compliance review and approval of tools and tactics; maintain oversight for IRB/EC approvals, as needed.
  • Ensure clear communications with all stakeholders throughout the process to ensure clearly defined expectations. Stakeholders include service providers, study and clinical teams, PSE team members, leadership, and compliance. Contribute to study meetings via facilitation, attending, and/or presenting at various meetings.
  • Maintain deep understanding and use of sponsor finance and contracting systems.
  • Support the coordination of congress / conference preparations and on-site logistics, as applicable
  • Ensure development and delivery of presentations and workshop content at Global Investigator Meetings, Ad Hoc face-to-face meetings, and other similar meetings as needed

Education and Experience Requirements:
  • BA/BS or equivalent, preferably in a scientific or health-related discipline.
  • Minimum of 3 years relevant experience in global patient recruitment and clinical trial execution with a pharmaceutical company, CRO, and/or healthcare facility/research site.
  • Strong clinical project management experience preferred
  • Expertise in the areas of drug development, clinical trial operations, and strategic planning.
  • Previous experience in clinical trial operations including the execution of study outreach, patient compliance and support programs.
  • Strong planning and tracking skills, customer focused, well organized, detail oriented and capable of successfully managing multiple projects.
  • Excellent time, priority, and self-management skills. Strong project management skills.
  • Strong team orientation: demonstrates initiative to solve problems and improve efficiency and/or customer service.
  • High degree of proficiency in Microsoft Excel, PowerPoint and Word. Microsoft Project.
  • Good written and oral communication skills.
  • Strong understanding of appropriate software and company systems.
  • Periodic travel as required

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 at https://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 $62,800.00 - $157,100.00. 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.

What IQVIA employees say

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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