Current jobs related to Medical Writer - sunnyvale - Raise

  • Technical Writer

    2 weeks ago

    Sunnyvale, California, United States Kelly Science, Engineering, Technology & Telecom Full time

    Job Title: Technical WriterWe are seeking a skilled Technical Writer to join our team at Kelly Science & Clinical. As a Technical Writer, you will be responsible for creating high-quality documentation for our client's in vitro diagnostic tests and instrument systems.Key Responsibilities:Develop and publish user manuals, guides, and other documentation for...

  • Technical Writer

    1 week ago

    sunnyvale, United States Kelly Science, Engineering, Technology & Telecom Full time

    Technical WriterShift: M-F, standard working hoursLocation: Sunnyvale, CA (hybrid)Pay: $50-60/hr6 month contract role to startOverview:The Technical Writer is responsible for writing, editing, formatting, and managing the publication and translation of customer-facing documents for in vitro diagnostic Xpert tests and GeneXpert instrument systems. Document...

  • Technical Writer

    2 weeks ago

    sunnyvale, United States Kelly Science, Engineering, Technology & Telecom Full time

    Technical WriterShift: M-F, standard working hoursLocation: Sunnyvale, CA (hybrid)Pay: $50-60/hr6 month contract role to startOverview:The Technical Writer is responsible for writing, editing, formatting, and managing the publication and translation of customer-facing documents for in vitro diagnostic Xpert tests and GeneXpert instrument systems. Document...

  • Technical Writer

    2 weeks ago

    Sunnyvale, United States Kelly Science, Engineering, Technology & Telecom Full time

    Technical WriterShift: M-F, standard working hoursLocation: Sunnyvale, CA (hybrid)Pay: $50-60/hr6 month contract role to startOverview:The Technical Writer is responsible for writing, editing, formatting, and managing the publication and translation of customer-facing documents for in vitro diagnostic Xpert tests and GeneXpert instrument systems. Document...

  • Technical Writer

    1 week ago

    Sunnyvale, United States Kelly Science, Engineering, Technology & Telecom Full time

    Technical WriterShift: M-F, standard working hoursLocation: Sunnyvale, CA (hybrid)Pay: $50-60/hr6 month contract role to startOverview:The Technical Writer is responsible for writing, editing, formatting, and managing the publication and translation of customer-facing documents for in vitro diagnostic Xpert tests and GeneXpert instrument systems. Document...

  • Life Sciences Technical Writer

    3 months ago

    Sunnyvale, United States Kelly Science, Engineering, Technology & Telecom Full time

    Kelly® Science & Clinical is seeking two experienced Technical Writers for a 6-month contract opportunity with a leading molecular diagnostics company at their headquarters in Sunnyvale, CA. If you are driven by the prospect of translating cutting-edge scientific discoveries into tangible advancements and are poised to advance your career, join us as we...

  • Technical Writer, Topic Based Writing

    1 week ago

    sunnyvale, United States Kelly Science, Engineering, Technology & Telecom Full time

    Kelly® Science & Clinical is seeking two experienced Technical Writers for a 6-month contract opportunity with a leading molecular diagnostics company at their headquarters in Sunnyvale, CA. If you are driven by the prospect of translating cutting-edge scientific discoveries into tangible advancements and are poised to advance your career, join us as we...

  • Technical Writer, Topic Based Writing

    2 weeks ago

    sunnyvale, United States Kelly Science, Engineering, Technology & Telecom Full time

    Kelly® Science & Clinical is seeking two experienced Technical Writers for a 6-month contract opportunity with a leading molecular diagnostics company at their headquarters in Sunnyvale, CA. If you are driven by the prospect of translating cutting-edge scientific discoveries into tangible advancements and are poised to advance your career, join us as we...

  • Technical Writer, Topic Based Writing

    1 week ago

    Sunnyvale, United States Kelly Science, Engineering, Technology & Telecom Full time

    Kelly® Science & Clinical is seeking two experienced Technical Writers for a 6-month contract opportunity with a leading molecular diagnostics company at their headquarters in Sunnyvale, CA. If you are driven by the prospect of translating cutting-edge scientific discoveries into tangible advancements and are poised to advance your career, join us as we...

  • Technical Writer

    4 weeks ago

    Sunnyvale, United States Juniper Networks Full time

    At Juniper, we believe the network is the single greatest vehicle for knowledge, understanding, and human advancement the world has ever known. To achieve real outcomes, we know that experience is the most important requirement for networking teams and the people they serve. Delivering an experience-first, AI-Native Network pivots on the creativity and...

  • Technical Content Specialist

    2 weeks ago

    Sunnyvale, California, United States Kelly Science, Engineering, Technology & Telecom Full time

    Job Title: Technical WriterJoin Kelly Science, Engineering, Technology & Telecom as a Technical Writer, responsible for creating high-quality documentation for in vitro diagnostic Xpert tests and GeneXpert instrument systems.Key Responsibilities:Develop and publish Instructions for Use, Quick Reference Instructions, User's Guides, and Getting Started...

  • Literary Agent

    3 weeks ago

    Sunnyvale, California, United States Crazy Maple Studio Full time

    Job Title: Literary AgentWe are seeking a highly skilled and well-connected Literary Agent to join our team at ReelShort Publishing House. As a key member of our team, you will be responsible for sourcing new and established romance authors, negotiating contracts, and managing author relationships.About UsReelShort Publishing House is part of ReelShort, a...

  • Product Manager

    4 weeks ago

    Sunnyvale, California, United States Walmart Full time

    Job SummaryWe are seeking a highly skilled Product Manager to join our Financial Services team at Walmart. As a Product Manager, you will be responsible for leading the roadmap and execution plan for our directed spend platform, leveraging our massive worldwide footprint to create an omni experience that meets our customers where they are.Key...

Medical Writer

2 months ago

sunnyvale, United States Raise Full time

We’re Hiring Our key client in clinical robotics is looking for additional members for their team. We have a Medical Writer (Clinical Evaluation Specialist) on the team.


Pay Rate: $70.00/hour on W2

Work Type: Hybrid – Onsite 2 days a week

Location: Sunnyvale, CA 94086

Duration: 3-month contract (with possible extension)


Job Overview:

  • This position reports to the Manager, Medical Science, and requires a strong candidate with experience in medical writing of clinical regulatory documents.
  • The position will mainly focus on supporting the in-house team with the Clinical Evaluation Reports (CERs), with the potential for future additional responsibility for developing other clinical evidence documents.
  • The purpose of this job is to support clinical evaluation reports (CERs) per Medical Device Regulation (MDR), to meet essential requirements in support of submission for CE Mark application to obtain Declaration of Conformity and EU market clearance, recertification and proposed indication/labeling changes, as well as CER updates to maintain EU product conformance.

Key Responsibilities:

  • Authoring sections of Clinical documentation as part of the Clinical Evaluation Reports [CER].
  • Acquire knowledge of therapeutic areas, literature review processes, and the ability to keep abreast of current literature.
  • Participates in and/or performs comprehensive literature searches to develop in-depth knowledge and understanding of current scientific literature required to support identified product lines and related clinical studies.
  • Work with the clinical librarian to help with conducting literature searches on products/product families.
  • Review the scientific literature and critically appraise and write clinical summaries for products and surgical procedures.
  • Support the internal team members by adhering to CER timelines and providing data on time to support global Regulatory activities.
  • Interacting with internal teams to understand the plan and strategy for developing the Clinical evaluation reports for new and existing products.
  • Conduct proofreading, editing, document formatting, review comment integration, and document completion/approval activities.
  • May assist with creation of clinical content including the preparation of manuscripts, scientific abstracts, conference presentations, and posters based on the company’s clinical trials.
  • May author Protocols and/or routine Clinical Study Progress Reports.
  • Ensure compliance with corporate (e.g., SOPs) and regulatory requirements (e.g., GCP and US and OUS guidelines)

Qualifications:

  • MD, PhD, or M.S. degree in a scientific field is desired.
  • Previous experience in the application of therapeutic and device knowledge to support the development of clinical evaluation reports.
  • Must have a minimum of 2-4 years of medical writing experience.
  • Minimum of 0-2 years of experience in clinical evaluation report writing in the medical device industry is preferred.
  • Strong experience in conducting literature searches, reviews, and appraisal of scientific data.
  • Demonstrated ability to clearly and effectively communicate verbally and in technical or scientific writing.
  • Demonstrated effective scientific writing skills.
  • Excellent critical and analytical thinking skills.
  • Must have a high level of attention to detail and accuracy.
  • Must be able to work effectively with internal team members.
  • Must be able to manage multiple projects across numerous surgical disciplines.
  • Strong communication, presentation, and interpersonal skills with high attention to detail and organization.
  • Strong experience in protocol development and writing clinical sections for regulatory submission.
  • Ability to learn quickly and self-educate on different surgical specialties as applicable to medical products and procedures (Self-starter attitude)
  • Consistently shows dedication or strong work ethic to help meet aggressive timelines or multiple projects when necessary.

Raise PBC is committed to a policy of nondiscrimination and equal opportunity for all employees and qualified applicants without regard to race, color, religious creed, national origin, ancestry, age, disability, genetics, gender identity, veterans' status, sexual orientation, or any other characteristic protected by law. Raise PBC is an equal-opportunity employer encouraging diversity in the workplace.