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Remote Clinical Trial Associate Jobs in Raleigh, NC

Working knowledge of clinical trial processes, GCP guidelines, and medical terminology ... This position is not eligible for employment sponsorship. #LI-CES and #LI-DNP #LI-HCP #remote IQVIA ...

... clinical trial design. The position will participate in the division's ongoing retrospective and ... remote). This position will involve analyzing patient data and coordinating analysis of patient ...

... clinical trial participants across the US. As of today, our board-certified physicians have ... This is a remote position with up to 25% domestic-travel. The Director of Business Development ...

... clinical trial participants across the US. As of today, our board-certified physicians have ... This is a remote position with up to 25% domestic-travel. The Director of Business Development ...

Freelance Independent Rater

Durham, NC · Remote

$62K - $156K/yr

... clinical trial experience and expertise in psychiatric assessments? We are expanding our global network of Central Independent Raters (CIRs) to support a depression study. 100% Remote Flexible ...

... clinical trial experience and expertise in psychiatric assessments? We are expanding our global network of Central Independent Raters (CIRs) to support a depression study. 100% Remote Flexible ...

... clinical trial experience and expertise in psychiatric assessments? We are expanding our global network of Central Independent Raters (CIRs) to support a depression study. 100% Remote Flexible ...

Freelance Independent Rater

Durham, NC · Remote

$62K - $156K/yr

... clinical trial experience and expertise in psychiatric assessments? We are expanding our global network of Central Independent Raters (CIRs) to support a depression study. 100% Remote Flexible ...

Showing results 41-60

Remote Clinical Trial Associate information

See Raleigh, NC salary details

$16

$38

$68

How much do remote clinical trial associate jobs pay per hour?

As of Sep 4, 2026, the average hourly pay for remote clinical trial associate 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 does a remote clinical trial associate do?

A Remote Clinical Trial Associate (CTA) supports the planning, execution, and management of clinical trials from a remote location. Their responsibilities include handling documentation, assisting with regulatory submissions, maintaining trial records, and coordinating communication between trial sites, sponsors, and regulatory bodies. Remote CTAs play a crucial role in ensuring that trials are conducted according to protocols, timelines, and regulatory requirements, all while working offsite. This allows for greater flexibility and can improve efficiency in clinical research processes.

What are the key skills and qualifications needed to thrive as a remote clinical trial associate, and why are they important?

To thrive as a Remote Clinical Trial Associate, you need a solid understanding of clinical research processes, regulatory guidelines, and typically a degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and Good Clinical Practice (GCP) certification are commonly required. Strong organizational skills, attention to detail, and effective communication are crucial soft skills for managing study documentation and collaborating with remote teams. These competencies ensure trials are conducted efficiently, compliantly, and with high data integrity in a virtual environment.

What are some common challenges faced by remote clinical trial associates, and how can they be managed?

Remote Clinical Trial Associates often encounter challenges such as maintaining consistent communication with on-site teams, managing multiple studies across different time zones, and ensuring accurate documentation while working virtually. These can be managed by leveraging robust digital communication tools, setting clear expectations for updates, and staying organized with project management software. Proactively building relationships with colleagues and participating in regular virtual meetings also helps ensure alignment and smooth coordination throughout the trial process.

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

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

What are popular job titles related to Remote Clinical Trial Associate jobs in Raleigh, NC?

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

Infographic showing various Remote Clinical Trial Associate job openings in Raleigh, NC as of August 2026, with employment types broken down into 1% As Needed, 70% Full Time, 26% Part Time, 1% Temporary, and 2% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $80,847 per year, or $38.9 per hour.

Clinical Research Associate II - Oncology - United States (Remote)

Worldwide Clinical Trials

Durham, NC • On-site, Remote

Full-time

Re-posted 13 days ago


Key responsibilities

  • Perform on-site and remote monitoring visits in accordance with protocol, GCP, ICH guidelines, and company SOPs

  • Build strong relationships with investigative sites and serve as a trusted partner

  • Review source documents, verify data accuracy, and support site activation, enrollment, maintenance, and closeout activities


Job description

Who we are

We're a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world's most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.

We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs - in the best possible way.

Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.

Why Worldwide

We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands-on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day.Join us!

What Clinical Operations does at Worldwide

At Worldwide Clinical Trials, we invite you to embark on a rewarding journey within Clinical Operations, where your contributions will leave a profound impact on the lives of patients.

Are you a motivated Clinical Research Associate with 2-3 years of monitoring experience who is looking for more than just your next job? Are you seeking a company that will invest in your development, provide meaningful career progression, and give you the opportunity to work alongside experienced clinical research professionals?

If so, we'd love to hear from you.

We are looking for a CRA II who is eager to expand their monitoring expertise, build strong site relationships, and grow into a senior clinical operations role. This position is ideal for someone who has established a solid foundation in site monitoring and is ready to accelerate their career within a supportive, collaborative, and quality-focused organization.

What you will do

As a CRA II, you will play a critical role in ensuring the successful execution of clinical trials by:

  • Performing on-site and remote monitoring visits in accordance with protocol, GCP, ICH guidelines, and company SOPs

  • Building strong relationships with investigative sites and serving as a trusted partner

  • Reviewing source documents and verifying data accuracy

  • Identifying risks, issues, and trends at sites and proactively driving resolution

  • Supporting site activation, enrollment, maintenance, and closeout activities

  • Ensuring patient safety, data integrity, and protocol compliance

  • Preparing detailed monitoring reports and follow-up letters

  • Collaborating cross-functionally with CTMs, project teams, and site personnel

What you will bring to the role

  • Excellent interpersonal, oral, and written communication skills in English

  • Superior organizational skills with attention to detail

  • Ability to work with little or no supervision

  • Proficiency in Microsoft Office, CTMS, and EDC Systems

Your experience

Required Qualifications

  • 2 - 3 years of experience as a regional, traveling Clinical Research Associate

  • 4-year universitydegree OR Nursing Degree

  • Knowledge of ICH-GCP guidelines and regulatory requirements

  • Experience conducting monitoring visits across multiple sites

  • Strong organizational, communication, and problem-solving skills

  • Ability to manage priorities in a fast-paced environment

  • Experience in Oncology is required

  • Willingness to travel regionally required

Preferred Qualifications

  • Experience in a CRO environment

  • Exposure to multiple therapeutic areas

  • Experience with decentralized or hybrid trial models

  • Desire to take on increasing responsibility and grow within Clinical Operations

At Worldwide Clinical Trials, we are committed to fostering an inclusive and equitable workplace by providing transparent compensation.
The salary range for this position is annually (For hourly paid positions, the stated salary range reflects hourly rates):


United States of America - $79,500.00 - $158,500.00


The salary range provided is intended to give candidates an understanding of potential earnings. Compensation will fall within the provided range, and it not a guarantee of exact salary. The final salary will be determined based on relevant experience, performance, education, and internal equity. In addition to base salary, we offer a competitive benefits package depending on location. We ensure pay equity and transparency and comply with all applicable labor laws. Salary information will be discussed during the interview process, and we encourage candidates to inquire about compensation at any stage.

We love knowing that someone is going to have a better life because of the work we do.

To view our other roles, check out our careers page at Discover a world of difference at Worldwide!For more information on Worldwide, visit www.Worldwide.com or connect with us on LinkedIn.