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Remote Clinical Investigator Jobs in Raleigh, NC

Remote based in the US Hours: Approximately 5h per week Role: Clinical Specialist Start: immediate ... Work closely with study investigators, site staff, and sponsor/CRO teams to support highquality ...

Remote based in the US Hours: Approximately 5h per week Role: Clinical Specialist Start: immediate ... Work closely with study investigators, site staff, and sponsor/CRO teams to support highquality ...

Collaborate with investigators, sponsors, monitors, and study team members to ensure protocol ... This position is not eligible for employment sponsorship. #LI-CES and #LI-DNP #LI-HCP #remote IQVIA ...

Drive advancement of technology-enabled clinical trial solutions, including workflow automation ... Support investigations, root cause analyses, and Corrective and Preventive Action (CAPA) activities.

Drive advancement of technology-enabled clinical trial solutions, including workflow automation ... Support investigations, root cause analyses, and Corrective and Preventive Action (CAPA) activities.

In this remote role you will serve as the primary country-level leader for clinical trial delivery ... Drive investigator engagement and site performance , including recruitment and retention strategies ...

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Remote Clinical Investigator information

See Raleigh, NC salary details

$34K

$54.5K

$98.2K

How much do remote clinical investigator jobs pay per year?

As of Aug 28, 2026, the average yearly pay for remote clinical investigator in Raleigh, NC is $54,491.00, according to ZipRecruiter salary data. Most workers in this role earn between $45,200.00 and $45,700.00 per year, depending on experience, location, and employer.

What is a remote clinical investigator?

A Remote Clinical Investigator is responsible for overseeing and analyzing clinical trial data, ensuring compliance with regulatory standards, and monitoring patient safety—all while working remotely. They collaborate with research teams, healthcare professionals, and regulatory bodies to assess trial integrity and effectiveness. Their duties may include reviewing medical records, identifying adverse events, and ensuring protocol adherence. This role requires strong analytical skills, clinical knowledge, and experience in research or regulatory compliance.

What does a remote clinical investigator do?

As a Remote Clinical Investigator, your day often includes reviewing clinical trial data, ensuring protocol compliance, and conducting remote site monitoring visits via video calls or secure digital platforms. You'll communicate regularly with study coordinators, sponsors, and regulatory agencies to resolve queries and address study-related issues. Documentation, data verification, and ongoing training to stay updated with regulations are also part of the workflow. This role offers flexibility and autonomy, but requires excellent organization to manage multiple studies and deadlines from a home or remote office environment.

What are the key skills and qualifications needed to thrive as a remote clinical investigator?

To excel as a Remote Clinical Investigator, you need a strong background in clinical research, data analysis, and regulatory compliance, usually supported by a degree in a health-related field. Familiarity with electronic data capture systems, Good Clinical Practice (GCP) certification, and experience using remote monitoring tools are highly valued. Exceptional organizational skills, attention to detail, and effective written and verbal communication are standout soft skills for this role. These competencies ensure rigorous study conduct, accurate data collection, and clear collaboration with sponsors, study sites, and regulatory bodies.

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

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

What cities near Raleigh, NC are hiring for Remote Clinical Investigator jobs?

Cities near Raleigh, NC with the most Remote Clinical Investigator job openings:

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

Durham, NC • On-site, Remote

Worldwide Clinical Trials
Scientific Research and Development Services • 10K+ employees

Full-time

Re-posted 6 days ago


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 Psychiatry 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.