Pharmaceutical Medical Writer - Oncology

HTC Global Services Inc

Remote, OR(remote)

JOB DETAILS
JOB TYPE
Full-time, Employee
SKILLS
Agile Programming Methodologies, Algorithms, Artificial Intelligence (AI), Biology, Biotech and Pharmaceutical, Brochures, Clinical Practices/Protocols, Clinical Research, Code of Federal Regulations, Communication Skills, Cross-Functional, Customer Relations, Develop and Maintain Customers, Documentation, Emerging Technology, FDA (Food and Drug Administration), HIPAA (Health Insurance Portability and Accountability Act), Health Science, Healthcare, Healthcare Software, Legal, Medical Equipment, Medical Products, Medical Writing, Medical and Scientific Writing, Medicine, Oncology, Product Design, Product Development, Product Planning, Product Requirements Document (PRD), Product Reviews, Publications, Regulations, Requirements Management, Requirements Validation/Verification, Sprint Planning, Technical Writing, Time Management, Training/Teaching Curriculum, Training/Teaching Materials, User Documentation, User Experience Design (UXD), User Interface Design, User Interface/Experience (UI/UX), White Papers, Writing Skills, eLearning
LOCATION
Remote, OR
POSTED
5 days ago

Scientific Medical Writer

Are you a Scientific Medical Writer with deep Oncology knowledge who enjoys working at the intersection of clinical science and technology? In this role, you will help shape a new healthcare platform by translating oncology workflows, scientific evidence, and clinical requirements into product guidance, training content, and high-quality scientific publications.

We are seeking a Scientific Medical Writer to serve as the clinical and scientific voice on a multidisciplinary product team comprised of AI and UI engineers. In this hybrid role, you will bridge the gap between clinical science and technology development — translating complex medical concepts into actionable product requirements and authoritative, audience-appropriate publications. You will play a central part in shaping a cutting-edge healthcare platform from the ground up.

Key Responsibilities

Clinical-Technology Requirements Definition

  • Partner with AI engineers and UI/UX designers to define, document, and validate product requirements at the intersection of clinical science and technology.
  • Translate clinical workflows, regulatory considerations, and scientific evidence into clear, implementable functional specifications.
  • Serve as the subject matter expert (SME) who ensures the platform's features, algorithms, and outputs align with clinical accuracy standards.
  • Participate in sprint planning, design reviews, and product roadmap sessions to provide a scientific perspective and flag clinical risks early.
  • Collaborate with clinical stakeholders to gather and synthesize input into requirements documentation.

Training Publications

  • Develop comprehensive training materials — including user guides, e-learning content, and quick-reference documentation — that effectively communicate platform functionality to clinical end-users.
  • Author scientifically grounded training curricula tailored to healthcare professionals, ensuring accuracy, clarity, and regulatory appropriateness.
  • Maintain and update training content in alignment with product iterations and evolving clinical evidence.

Customer-Facing Manuscripts & Content

  • Write and edit peer-reviewed manuscripts, white papers, and case studies that demonstrate the clinical value, evidence base, and real-world outcomes of the platform.
  • Develop customer-facing scientific communications, including product brochures, clinical summaries, and conference abstracts.
  • Ensure all publications meet journal submission standards, adhere to ICMJE authorship guidelines, and comply with applicable regulatory and promotional requirements.
  • Manage publication timelines and coordinate with internal teams and external authors or KOLs as needed.

Qualifications

Required

  • Advanced degree in a life sciences, health sciences, or clinical discipline (Ph.D., PharmD, MD, or Master's with significant industry experience).
  • 3+ years of medical writing experience in a healthcare technology, pharmaceutical, biotech, or clinical research environment.
  • Demonstrated ability to produce high-quality regulatory, scientific, or technical documents on deadline.
  • Strong understanding of clinical research methodology, evidence-based medicine, and healthcare data.
  • Comfortable working in agile or sprint-based product development environments.

Preferred

  • Experience writing requirements documentation or user stories for healthcare software or SaMD (Software as a Medical Device).
  • Familiarity with AI/ML concepts as applied in clinical or diagnostic settings.
  • Working knowledge of regulatory frameworks such as FDA 21 CFR, EU MDR, or HIPAA.
  • AMWA or ISMPP certification, or equivalent professional credentials.
  • Prior experience engaging with Key Opinion Leaders (KOLs) for manuscript development.
  • Oncology background/experience required

What Makes HTC A Great Place To Build Your Future

HTC Global Services wants you to join our team. Come build new things with us and advance your career. At HTC Global, you’ll collaborate with experts, work alongside clients, and be part of high-performing teams driving success together. You’ll have long-term opportunities to grow your career and develop skills in the latest emerging technologies.

At HTC Global Services, our employees have access to a comprehensive benefits package. Benefits can include Group Health (Medical, Dental, and Vision), Paid Time Off, Paid Holidays, 401(k) matching, Group Life and Disability insurance, Professional Development opportunities, Wellness programs, and a variety of other perks.

Our success as a company is built on inclusion and diversity. HTC Global Services is committed to providing a workplace free from discrimination and harassment, where every employee is treated with dignity and respect. We celebrate differences and believe that diverse cultures, perspectives, and skills drive innovation and success. HTC is an Equal Opportunity Employer and a proud National Minority Supplier. We seek to empower each individual, fostering an environment where everyone feels valued, included, and respected.

For information on the compensation range for the job and an overview on benefits that HTC Global Services offers please email compensationrange@htcinc.com.  The salary, other compensation and benefits information shared by HTC would be accurate as of the date of sharing the information.  The disclosed range would consider factors not limited to, geographic location, educational qualification, relevant experience, certifications, skills, suitability/fit for the role, and business or organizational needs. HTC Global services reserves the right to modify the ranges at any time, subject to applicable law.

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About the Company

H

HTC Global Services Inc

INDUSTRY
Computer/IT Services