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Remote Life Science Editor Jobs in Oregon (NOW HIRING)

Life Sciences Location: US or Canada (Hybrid/Remote) Position Overview The Research Associate/Senior Research Associate, Real World Evidence (RWE) is part of the global Real World & Late Phase (RWLP ...

Remote Travel Expectations: 0% Job Classification: Temporary (W2T) Join Centric Consulting - A ... This is how we bringour mission and core values to life, working together to provide the ...

Data Scientist 1

OR · On-site +1

$95K - $115K/yr

College degree in Computer Science, Information Science or related field preferred - OR ... Voluntary Life Insurance (Employee/Spouse/Child) * Employer Paid Short & Long Term Disability

... science into clear, accurate, audience-friendly explanations. You will work closely with our social ... Video editing skills (not required since we have an editor, but a plus) Logistics * Engagement type ...

Principal Technical Specialist

Portland, OR · On-site +1

$140K - $165K/yr

Are you ready to accelerate your potential and make a real difference within life sciences ... We recognize the benefits of flexible, remote working arrangements for eligible roles and are ...

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Remote Life Science Editor information

What are Remote Life Science Editors?

Remote Life Science Editors are professionals who work from a remote location to review, edit, and improve scientific manuscripts, articles, and reports in the life sciences field. Their responsibilities often include checking for accuracy, clarity, grammar, and adherence to journal or publication guidelines. These editors help researchers and scientists communicate their findings effectively, ensuring that manuscripts are well-organized and scientifically sound before publication. They may work for academic journals, publishing houses, or as freelancers. Strong backgrounds in biology, medicine, or related fields and excellent language skills are typically required.

What are some common challenges faced by Remote Life Science Editors, and how can they be managed effectively?

Remote Life Science Editors often encounter challenges such as managing tight deadlines across multiple projects and ensuring clear communication with authors and team members in different time zones. Staying organized with task management tools and setting clear expectations with collaborators can help overcome these hurdles. Additionally, keeping current with the latest research and industry guidelines is essential for maintaining high editorial standards. Proactive communication and continuous professional development are key to succeeding in this dynamic, remote role.

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

To thrive as a Remote Life Science Editor, you need a strong background in life sciences, excellent command of the English language, and experience with scientific writing and editing, often supported by an advanced degree (e.g., MSc or PhD). Familiarity with reference management tools, editing software such as Microsoft Word with track changes, and guidelines like AMA or APA is typically required. Attention to detail, time management, and clear communication are critical soft skills for managing deadlines and collaborating with researchers. These skills ensure the delivery of high-quality, publication-ready manuscripts and effective remote teamwork.

What is the difference between Remote Life Science Editor vs Remote Medical Writer?

AspectRemote Life Science EditorRemote Medical Writer
Required credentialsAdvanced degree in life sciences, editing certificationsAdvanced degree in life sciences, writing certifications
Work environmentEditing scientific content, peer review, manuscript preparationWriting scientific documents, clinical study reports, regulatory submissions
Employer & industry usagePublishers, research institutions, biotech companiesPharmaceutical companies, CROs, regulatory agencies
Common search & comparison intentUnderstanding editing roles in life sciencesUnderstanding writing roles in life sciences

While both roles require a strong background in life sciences, Remote Life Science Editors focus on reviewing and refining scientific content, ensuring clarity and accuracy. Remote Medical Writers primarily create and compose scientific documents, such as clinical reports and regulatory submissions. Both roles often work in similar environments and require advanced degrees, but their core responsibilities differ in content creation versus editing.

What are popular job titles related to Remote Life Science Editor jobs in Oregon? For Remote Life Science Editor jobs in Oregon, the most frequently searched job titles are:
What job categories do people searching Remote Life Science Editor jobs in Oregon look for? The top searched job categories for Remote Life Science Editor jobs in Oregon are:
What cities in Oregon are hiring for Remote Life Science Editor jobs? Cities in Oregon with the most Remote Life Science Editor job openings:
Senior Research Associate

Senior Research Associate

Syneoshealth

OR • On-site, Remote

Full-time

Posted 4 days ago


Syneos Health rating

8.3

Company rating: 8.3 out of 10

Based on 21 frontline employees who took The Breakroom Quiz

24th of 73 rated pharmaceutical


Job description

Senior Research Associate

Syneos Health is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress.
Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape.
Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you'll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to deliver - for one another, our customers, and, most importantly, for those in need.
Discover what your 25,000 future colleagues already know:
Why Syneos Health
We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.
We are committed to building an inclusive culture - where you can authentically be yourself. Central to this is our purpose - Driven to Deliver - which captures the passion of our colleagues to show up each day and shape solutions that have the ability to dramatically impact someone's life.
We are continuously building the company we all want to work for and our customers want to work with. Why? Because we know that when we bring together smart colleagues from across the world, we can shape the future of healthcare, driving impact for customers and defining the pace of patient progress.

Job Responsibilities

JOB TITLE: Research Associate/Senior Research Associate, Real World Evidence

SELECT ONE: Clinical Solutions

JOB CODE: SH1317/ SH1323

REPORTS TO: Associate Director, Real World Evidence; or designee

Business Unit: Real World & Late Phase (RWLP)
Industry: Life Sciences
Location: US or Canada (Hybrid/Remote)

Position Overview

The Research Associate/Senior Research Associate, Real World Evidence (RWE) is part of the global Real World & Late Phase (RWLP) Business Unit, supporting the generation of real-world evidence, and patient outcomes evidence across the drug development lifecycle.

In this role, you will contribute to and or lead real-world research initiatives that inform clinical strategy, regulatory engagement, and market access decisions for life sciences clients. Working closely with senior team members, you will support the design and execution of retrospective and prospective studies while developing your expertise in RWE and outcomes research methodologies.

This position is well suited to professionals seeking meaningful exposure to or to deepen their expertise in evidence generation within a collaborative, well-supported team environment that values high-quality work and sustainable performance.

Key Responsibilities

  • Contribute to study design and methodology development
  • Develop innovative approaches, frameworks and solutions to client problems
  • Deliver project outputs that meet established quality standards, timelines, and budget requirements.
  • Conduct structured literature reviews and targeted secondary research to support RWE initiatives.
  • Participate in qualitative research activities, including patient interviews, to generate actionable healthcare insights.
  • Analyze and interpret qualitative and quantitative 'real-world' data for deliverables
  • Conduct workshops and moderate discussions
  • Present results to external clients
  • Contribute to the development of:
    • Study protocols
    • Technical reports
    • Manuscripts and scientific posters
    • Client presentations
  • Develop and format materials using PowerPoint, Word, and Excel.
  • Summarize and synthesize complex clinical and outcomes data into clear, structured findings.
  • Support retrospective and prospective real-world studies under senior guidance.
  • Demonstrate openness to leveraging emerging technologies, including AI-enabled tools, to improve efficiency, analytical rigor, and personal productivity.

Qualifications

Required

  • Master's degree in public health, epidemiology, health sciences, or a related field (or equivalent combination of education and experience).
  • 1-2 years (Research Associate), or 2+ years (Senior Research Associate) of relevant experience within the life sciences industry (e.g., HEOR, RWE, clinical research, pharmaceutical industry, healthcare consulting, or academia).
  • Foundational understanding of real-world research methodologies and study design.
  • Overall understanding of the drug development lifecycle.
  • Strong analytical and critical thinking skills.
  • Proficiency in Microsoft Excel, Word, and PowerPoint.
  • Working knowledge of statistical software (e.g., SAS, R, Stata, or similar).
  • Business-level conversational English (written and spoken).

Preferred

  • Graduate degree (Master's or PhD) in a relevant discipline.
  • Academic or industry research experience.
  • Conducting analyses in databases and/or registries

Key Competencies

  • Clear and professional communication skills
  • Strong teamwork and collaboration
  • Attention to detail and commitment to quality
  • Ability to manage multiple priorities in a structured, deadline-driven environment
  • Intellectual curiosity and commitment to continuous improvement, including adoption of new technologies
  • Willingness to travel (~10%)

Work Environment

As part of a global RWLP team, you will work within an international, cross-functional environment with access to experienced mentors and structured development opportunities. Our hybrid model offers flexibility, and our team culture emphasizes high standards, collaboration, and sustainable performance to support long-term career growth in the life sciences industry.

Get to know Syneos Health


Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients.

No matter what your role is, you'll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health.

http://www.syneoshealth.com

Additional Information


Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.


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