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Remote Clinical Scientist Jobs in Raleigh, NC (NOW HIRING)

Danaher

Principal Clinical Scientist

Raleigh, NC · On-site +1

Principal Clinical Scientist . This role is responsible for clinical trial strategies within the US ... We recognize the benefits of flexible, remote working arrangements for eligible roles and are ...

ICON

Senior Clinical Scientist

Raleigh, NC · On-site +1

Senior Clinical Scientist (Hematology-Oncology) ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients ...

Agilent

Clinical Affairs Scientist

Durham, NC · On-site +1

$105K - $197K/yr

We are searching for an experienced Clinical Affairs Scientist (CAS) to work within the medical diagnostic field as a key member of the Organization of Chief Medical Officer(OCMO) Global Clinical ...

IQVIA

Clinical Trial Rater

Durham, NC · Remote

Flexible, remote work schedule. * Opportunity to contribute to global clinical research. * Collaborate with a team committed to improving patient care and advancing science. #LI-DNP #LI-Remote #LI ...

IQVIA

Clinical Trial Rater

Raleigh, NC · Remote

Flexible, remote work schedule. * Opportunity to contribute to global clinical research. * Collaborate with a team committed to improving patient care and advancing science. #LI-DNP #LI-Remote #LI ...

Allucent

Clinical Trial Lead

Cary, NC · On-site +1

We are looking for a Clinical Trial Leader (CTL) to join our A-team (office-based*/remote). As a ... A degree in life sciences or nursing qualification preferred, but notrequired. * A minimum of5years ...

Allucent

Clinical Trial Lead

Cary, NC · Remote

We are looking for a Clinical Trial Leader (CTL) to join our A-team (office-based*/remote). As a ... A degree in life sciences or nursing qualification preferred, but not required. * A minimum ...

Allucent

Clinical Trial Lead

Cary, NC · On-site +1

We are looking for a Clinical Trial Leader (CTL) to join our A-team (office-based*/remote). As a ... A degree in life sciences or nursing qualification preferred, but not required. * A minimum of 5 ...

Berriehill Research

Senior Scientist

Raleigh, NC · On-site +1

$80K - $110K/yr

Remote work may be considered for the right candidate. What you will do as a senior scientist: * Develop and use engineering computer codes such as wind/storm surge/wave hazard models and engineering ...

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Remote Clinical Scientist information

See Raleigh, NC salary details

$25

$48

$72

How much do remote clinical scientist jobs pay per hour?

As of Sep 8, 2026, the average hourly pay for remote clinical scientist in Raleigh, NC is $48.40, according to ZipRecruiter salary data. Most workers in this role earn between $35.48 and $60.34 per hour, depending on experience, location, and employer.

What is a remote clinical scientist?

A Remote Clinical Scientist conducts clinical research, analyzes data, and supports drug or therapy development while working remotely. They collaborate with cross-functional teams, including medical, regulatory, and biostatistics professionals, to ensure study integrity and compliance. Responsibilities may include protocol development, clinical trial monitoring, and scientific data interpretation. This role typically requires expertise in clinical research, regulatory guidelines, and therapeutic areas relevant to the employer’s focus. It allows professionals to contribute to clinical advancements without being tied to a physical location.

How does a remote clinical scientist collaborate with onsite teams and manage project responsibilities from a distance?

Remote Clinical Scientists work closely with clinical research associates, data managers, and investigators through frequent virtual meetings, collaborative platforms, and electronic documentation tools. They are responsible for reviewing data, monitoring trial progress, ensuring protocol compliance, and addressing site queries, all while maintaining regular communication with onsite staff. This remote setup requires proactive scheduling, timely reporting, and strong organizational skills to stay aligned with project milestones. The ability to leverage digital communication tools ensures effective teamwork and consistent project oversight despite physical distance.

What are the key skills and qualifications needed to thrive in the remote clinical scientist position, and why are they important?

To excel as a Remote Clinical Scientist, you typically need an advanced degree in a life science field, experience in clinical research, and strong data analysis skills. Familiarity with electronic data capture (EDC) systems, clinical trial management software, and regulatory requirements such as GCP is crucial, as are relevant certifications like SOCRA or ACRP. Excellent communication, self-motivation, and problem-solving abilities set apart top candidates in this remote role. These skills ensure the effective oversight of clinical trials, compliance with regulations, and successful remote collaboration with multidisciplinary teams.

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

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

What job categories do people searching Remote Clinical Scientist jobs in Raleigh, NC look for?

The top searched job categories for Remote Clinical Scientist jobs in Raleigh, NC are:

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

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

Remote Clinical Scientist jobs near you
Infographic showing various Remote Clinical Scientist job openings in Raleigh, NC as of September 2026, with employment types broken down into 100% Full Time. Highlights an 100% Remote job distribution, with an average salary of $100,675 per year, or $48.4 per hour.

Clinical Scientist

Durham, NC • On-site, Remote

Worldwide Clinical Trials
Scientific Research and Development Services • 10K+ employees
Learn more about Worldwide Clinical Trialsexternal

Full-time

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 the Clinical Scientist does at Worldwide
The Clinical Scientist is responsible for the review, interpretation, and assessment of clinical data with key findings communicated to Clients and study team. The Clinical Scientist works closely with the Medical Monitor as appropriate. This role communicates and presents clinical trends and findings to the Study Team and Clients while working collaboratively to ensure high quality data, maintain the highest integrity of the clinical database and clinical study reports (e.g., CSR). The Clinical Scientist partners with Clients, subcontractors, and internal study team members to meet project timelines and expectations related to clinical data review.
What you will do
  • Develop clinical data review plans for assigned studies.
  • Collaborate with cross-functional study team members to ensure protocol-defined variables are collected and reported accurately.
  • Conduct ongoing review and analysis of clinical data, (e.g., efficacy, safety related data components) utilizing listings, tables, figures, graphs, and EDC as needed.
  • Track and analyze potential safety events in collaboration with Pharmacovigilance and Medical Monitoring.
  • Contribute to discussions on potential study or strategy modifications based on clinical data review.
  • Create data summary slides for Safety Review Committee Meetings, Data Review Meetings with support from Director.
  • Present key data trends and findings to the Medical Monitor, Study Team, and Client.
  • Query data as appropriate on EDC data as needed during Clinical review with timely follow up, and identification of potential protocol deviations.
  • Partner with vendors and study team members to ensure accurate endpoint reporting.
  • Serve as a point of contact for site staff and monitors for protocol and clinical inquiries.
  • Collaborate with Data Management on CRF design, CRF instructions, and data quality plans.
  • Review data-driven sections of regulatory and clinical reporting documents (e.g., CSRs, INDs, NDAs/BLAs, annual reports, IBs, etc.).
  • Provide scientific writing support, including patient narratives, abstracts, posters, and presentations.
  • Mentor and train junior staff.
  • Utilize visual analytics tools to interpret and communicate data insights.

The duties and responsibilities listed above are representative of the nature and level of work assigned and are not necessarily all-inclusive.
What you bring to the role
  • Strong knowledge of clinical development processes and study design principles.
  • Deep understanding of product profiles and safety concepts.
  • Skilled in clinical data analysis, interpretation, and assessing clinical relevance in human clinical trials, within the relevant therapeutic area.
  • Proficient with electronic data capture systems and data visualization tools.
  • Solid understanding of GCP, ICH guidelines, and regulatory requirements.
  • Excellent written, oral communication, and presentation skills.
  • Strong organizational, analytical, and problem-solving abilities.
  • Ability to manage multiple priorities and adapt to changing demands.
  • Strong interpersonal skills and the ability to collaborate across teams and levels.
  • Demonstrated ability to work independently and within teams.
  • Good judgment and decision-making skills.
  • Willingness to travel as needed.

Your experience
  • Advanced clinical or scientific degree preferred (e.g., PharmD, PhD, MSN, MPH) with 8+ years of industry-related experience in Oncology
  • OR Bachelor's degree with 12+ years of relevant industry/research experience in the relevant therapeutic area, including data review and interpretation.
  • Proficiency in Microsoft Office Suite.
  • Experience with EDC systems and data visualization platforms.

Promotion to the next level is not automatic based on years of experience. Personnel are evaluated on proven competency, level of responsibility, and ability to work independently.
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 - $79,000.00 - $157,000.00
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.

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