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

IQVIA

Clinical Research Coordinator

Raleigh, NC · Remote

$35 - $42/hr

... remote 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 ...

COMPASS Pathways

HEOR Science Liaison

Raleigh, NC · On-site +1

$63K - $85K/yr

Location: Remote in the United States. Reports to: Director, HEOR. Roles and responsibilities ... Deliver fair-balanced, scientifically rigorous presentations on clinical data, real-world evidence ...

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Remote Clinical Scientist information

See Raleigh, NC salary details

$27

$53

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How much do remote clinical scientist jobs pay per hour?

As of Jul 28, 2026, the average hourly pay for remote clinical scientist in Raleigh, NC is $53.22, according to ZipRecruiter salary data. Most workers in this role earn between $39.04 and $66.35 per hour, depending on experience, location, and employer.

What is a Remote Clinical Scientist job?

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:
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Remote Clinical Scientist jobs near you
Infographic showing various Remote Clinical Scientist job openings in Raleigh, NC as of July 2026, with employment types broken down into 93% Full Time, 5% Part Time, and 2% Contract. Highlights an 100% Remote job distribution, with an average salary of $110,692 per year, or $53.2 per hour.
Clinical Scientist - Oncology - US - Remote

Clinical Scientist - Oncology - US - Remote

Worldwide Clinical Trials

Durham, NC • On-site, Remote

Full-time

Posted 11 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
As a member of the Clinical Oncology Operations team, the Clinical Scientist leads the review and assessment of clinical data, ensuring it meets the highest standards of quality and integrity. This role translates complex data into clear insights, communicates trends to internal teams and clients, and supports the development of key regulatory deliverables such as clinical study reports. Working closely with cross-functional stakeholders, the Clinical Scientist helps drive timely project delivery, contributes to data review strategies, and identifies opportunities to improve processes and elevate overall study execution.
What you will do
  • Partner with cross-functional Study Teams (Medical, Biostatistics, Data Management) to develop and execute data review plans, ensuring accurate collection and reporting of protocol-defined endpoints.

  • Perform ongoing review and interpretation of clinical data (efficacy and safety) across listings and visual analytics, identifying trends and generating actionable insights.

  • Monitor and analyze safety events across studies and programs, supporting risk identification, escalation, and informed decision-making.

  • Communicate and present clinical findings, trends, and recommendations to Study Teams, Medical leadership, and clients; contribute to strategic discussions and study modifications.

  • Support development of key deliverables, including clinical study reports (CSRs), regulatory documents (e.g., INDs, NDAs/BLAs, IBs), and data summaries for SRCs, DSMBs, and internal review meetings.

  • Collaborate on CRF design, data quality processes, and EDC query management; identify protocol deviations and ensure data integrity in partnership with internal teams and vendors.

  • Contribute to study execution and continuous improvement efforts, including dashboard/UAT support, study documentation, scientific writing (e.g., narratives, abstracts), and mentoring of junior staff.

What you will bring to the role
  • Strong knowledge of the clinical development process, study design principles, and product safety profiles.

  • Experience in clinical data analysis, interpretation, and translating insights into clinical relevance.

  • Proficiency with electronic data capture (EDC) systems, data visualization tools, and Microsoft Office (Excel, PowerPoint, Word).

  • Solid understanding of GCP, ICH, and applicable regulatory requirements.

  • Excellent communication and presentation skills, with the ability to convey complex data clearly to diverse stakeholders.

  • Strong organizational, analytical, and problem-solving skills, with the ability to manage multiple priorities and meet deadlines.

  • Collaborative, adaptable team player with strong interpersonal skills and the ability to work effectively across all levels of an organization.

  • Sound judgment, high attention to detail, and the ability to work both independently and in fast-paced, evolving environments.

Your experience
  • Advanced clinical/science degree (e.g., PharmD, PhD, MSN, MPH, etc.) preferred.

  • 8+ of industry/related experience in Oncology human clinical trial research including review and interpretation of clinical data.

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.
Worldwide is an equal opportunity employer that is committed to enabling professionals from all backgrounds and experiences to succeed and, to that end, we prioritize attracting diverse talent and cultivating an inclusive environment that encourages collaboration and creativity. We know that when our employees feel appreciated and included, they can be more creative, innovative, and successful. We're on a mission to hire the very best and are committed to creating exceptional employee experiences where everyone is respected and has access to equal opportunity. We provide equal employment opportunities to all employees and applicants regardless of race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or other class protected by applicable law

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