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Remote Scientific Writing Jobs in Raleigh, NC (NOW HIRING)

Contemporaries

Data Scientist

Durham, NC · Remote

$51 - $58/hr

This is a long-term contract opportunity offering remote work flexibility. We are looking for ... technical writing, editing, and interpretation of findings * Provide scientific guidance ...

GlaxoSmithKline

Principal Medical Writer

Durham, NC · On-site +1

... scientific field. * 5+ years of experience in medical or regulatory writing within the ... Experience working in multicultural or remote team settings. * Proven ability to independently ...

ViiV Healthcare

Principal Medical Writer

Durham, NC · On-site +1

... scientific field. * 5+ years of experience in medical or regulatory writing within the ... Experience working in multicultural or remote team settings. * Proven ability to independently ...

Trilogy

Senior/Principal Medical Writer - USA

Durham, NC · On-site +1

$120K - $159K/yr

Trilogy Writing & Consulting,anIndegeneCompany, ishiring Senior/Principal Medical Writers (USA) to ... A minimum of aBachelor's degree in science/pharmacy (Ph.D. not necessary). * Fluent written and ...

Hitachi

Research Scientist - Power Systems

Raleigh, NC · On-site +1

Engineering & Science Job Schedule: Full time Remote: No Research Scientist - Power Systems The ... Fluency in English, both written and spoken. * Fluency in common programming languages like Python ...

Darkhorse Tech

IT Field Technician (Remote)

Raleigh, NC · Remote

$43K - $50K/yr

Excellent verbal and written communication * Proven time management skills * Proven reliability and ... Bachelor's degree in Information Technology or Computer Science is preferred * Must have reliable ...

WIRB-Copernicus Group (WCG)

CTMS Analyst (Remote)

Cary, NC · On-site +1

$73K - $114K/yr

WCG is proud to serve individuals on the frontlines of science and medicine, and the organizations ... Excellent communication (oral/written) and interpersonal skills. * Preferred but not required:

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Remote Scientific Writing information

See Raleigh, NC salary details

$10.7K

$68.5K

$77.3K

How much do remote scientific writing jobs pay per year?

As of Jun 17, 2026, the average yearly pay for remote scientific writing in Raleigh, NC is $68,531.00, according to ZipRecruiter salary data. Most workers in this role earn between $65,100.00 and $71,900.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in the Remote Scientific Writing position, and why are they important?

To thrive in Remote Scientific Writing, you need strong research, analytical, and technical writing skills, usually backed by a degree in a scientific discipline. Familiarity with reference management software like EndNote or Mendeley, as well as proficiency in formatting and submitting manuscripts for scientific journals, is often required. Being detail-oriented, self-motivated, and possessing excellent communication skills are important soft skills for this role. These abilities are critical for producing clear, accurate, and publishable scientific documents while working independently and meeting tight deadlines remotely.

What are some typical daily responsibilities for a Remote Scientific Writing position?

In a Remote Scientific Writing role, your daily tasks often include researching scientific literature, drafting and editing manuscripts, and ensuring documents adhere to specific journal or publication guidelines. You may also collaborate remotely with researchers, editors, and subject matter experts to clarify technical content or gather additional data. Adhering to deadlines and managing multiple projects at once are common aspects of this role. Regular communication through email, project management tools, and virtual meetings is essential for coordination and feedback, even while working independently.

What is a Remote Scientific Writing job?

A Remote Scientific Writing job involves creating and editing scientific content, such as research papers, grant proposals, regulatory documents, or educational materials, from a remote location. Writers typically work for research institutions, pharmaceutical companies, or scientific publishers. This role requires strong writing skills, domain-specific knowledge, and the ability to communicate complex scientific concepts clearly. Many remote scientific writers have advanced degrees in science, medicine, or engineering.

What are popular job titles related to Remote Scientific Writing jobs in Raleigh, NC? For Remote Scientific Writing jobs in Raleigh, NC, the most frequently searched job titles are:
What job categories do people searching Remote Scientific Writing jobs in Raleigh, NC look for? The top searched job categories for Remote Scientific Writing jobs in Raleigh, NC are:
What cities near Raleigh, NC are hiring for Remote Scientific Writing jobs? Cities near Raleigh, NC with the most Remote Scientific Writing job openings:
Remote Scientific Writing jobs near you
Infographic showing various Remote Scientific Writing job openings in Raleigh, NC as of June 2026, with employment types broken down into 75% Full Time, and 25% Part Time. Highlights an 100% Remote job distribution, with an average salary of $68,531 per year, or $32.9 per hour.
Clinical Scientist - Oncology - US - Remote

Clinical Scientist - Oncology - US - Remote

Worldwide Clinical Trials

Durham, NC • On-site, Remote

Full-time

Posted 29 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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