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Remote Biological Science Writer Jobs in Raleigh, NC

IQVIA

Senior Data Team Lead (Remote)

Raleigh, NC · Remote

$86K - $217K/yr

Bachelor's degree in life sciences, health, clinical, biological, or mathematical field. * No less ... Fully remote role - company equipment provided * Competitive salary and performance-based ...

IQVIA

Senior Data Team Lead (Remote)

Durham, NC · Remote

$86K - $217K/yr

Bachelor's degree in life sciences, health, clinical, biological, or mathematical field. * No less ... Fully remote role - company equipment provided * Competitive salary and performance-based ...

IQVIA

Senior Data Team Lead (Remote)

Durham, NC · Remote

$86K - $217K/yr

Bachelor's degree in life sciences, health, clinical, biological, or mathematical field. * No less ... Fully remote role - company equipment provided * Competitive salary and performance-based ...

IQVIA, Inc.

Senior Data Team Lead (Remote)

Durham, NC · On-site +1

$86K - $217K/yr

Bachelor's degree in life sciences, health, clinical, biological, or mathematical field. * No less ... Fully remote role - company equipment provided * Competitive salary and performance-based ...

IQVIA

Senior Data Team Lead (Remote)

Raleigh, NC · Remote

$86K - $217K/yr

Bachelor's degree in life sciences, health, clinical, biological, or mathematical field. * No less ... Fully remote role - company equipment provided * Competitive salary and performance-based ...

Danaher

Senior Engineer, Process Validation

Raleigh, NC · On-site +1

$100K - $130K/yr

We bring together deep scientific expertise, an unwavering commitment to quality, and a ... Proficiency in technical writing with deviation investigations, root cause analysis, and risk ...

IQVIA

AI Solutions Architect (Remote)

Durham, NC · On-site +1

$61 - $80.25/hr

Master's degree or PhD in Computer Science, Bioinformatics, Computational Biology, Data Science, Engineering, ora relatedfield. * Significant experiencedelivering AI, data, analytics, or digital ...

IQVIA, Inc.

AI Solutions Architect (Remote)

Durham, NC · On-site +1

$61 - $80.25/hr

Master's degree or PhD in Computer Science, Bioinformatics, Computational Biology, Data Science, Engineering, or a related field. * Significant experience delivering AI, data, analytics, or digital ...

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Remote Biological Science Writer information

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How much do remote biological science writer jobs pay per hour?

As of Jul 15, 2026, the average hourly pay for remote biological science writer in Raleigh, NC is $45.80, according to ZipRecruiter salary data. Most workers in this role earn between $32.69 and $57.02 per hour, depending on experience, location, and employer.

What does a Remote Biological Science Writer do?

A Remote Biological Science Writer creates scientific content related to biology, such as articles, reports, research summaries, or educational materials, while working from a location outside of a traditional office. They interpret complex biological research and translate it into clear, accessible language for various audiences, including scientists, healthcare professionals, and the general public. This role often involves collaborating with researchers, staying updated on scientific advancements, and ensuring accuracy and clarity in all written materials.

What are the key skills and qualifications needed to thrive as a Remote Biological Science Writer, and why are they important?

To thrive as a Remote Biological Science Writer, you need a solid background in biological sciences, excellent writing abilities, and typically at least a bachelor’s degree in a relevant field. Familiarity with scientific literature databases, reference management tools (like EndNote or Zotero), and proficiency in word processing and collaboration platforms are essential. Strong attention to detail, time management, and the ability to translate complex scientific concepts into clear, engaging language make someone stand out in this role. These skills ensure accurate, accessible content that meets publication standards and effectively communicates scientific information to varied audiences.

How does a Remote Biological Science Writer typically collaborate with researchers and editorial teams while working offsite?

As a Remote Biological Science Writer, you will frequently communicate with researchers, subject matter experts, and editorial teams through email, video conferencing, and project management tools. Regular virtual meetings help clarify project objectives, review scientific content, and ensure accuracy in interpretations. You may also participate in collaborative document editing and receive feedback through shared platforms to maintain alignment with publication standards. Building strong digital communication skills and being proactive in seeking input are essential for success in this remote, team-oriented environment.
What are the most commonly searched types of Biological Science Writer jobs in Raleigh, NC? The most popular types of Biological Science Writer jobs in Raleigh, NC are:
What are popular job titles related to Remote Biological Science Writer jobs in Raleigh, NC? For Remote Biological Science Writer jobs in Raleigh, NC, the most frequently searched job titles are:
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Remote Biological Science Writer jobs near you
Clinical Scientist - Oncology - US - Remote

Clinical Scientist - Oncology - US - Remote

Worldwide Clinical Trials

Durham, NC • On-site, Remote

Full-time

Re-posted 27 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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