CrawlJobs Logo

Medical Writer, Scientific Communications

vaniamgroup.com Logo

Vaniam Group

Location Icon

Location:
United States

Category Icon

Job Type Icon

Contract Type:
Not provided

Salary Icon

Salary:

70000.00 - 85000.00 USD / Year

Job Description:

The Medical Writer, Scientific Communications is responsible for writing strategically aligned and accurate materials that meet the high-quality standards of Vaniam Group. You will play a supporting role in managing client satisfaction and relationships. In addition, you are responsible for supporting business improvement by meeting personal and departmental goals and objectives effectively and on time.

Job Responsibility:

  • Develop high-quality content for an array of projects, including publications (eg, abstracts, presentations, and manuscripts), advisory boards, scientific platforms, gap analyses, literature summaries, slide sets, and training materials
  • Develop materials that are grammatically accurate and audience appropriate
  • Gain an understanding of the treatment landscape and strategic positioning of client products to help produce strategically aligned materials
  • Assess project needs and challenges
  • identify and implement solutions to meet productivity, quality, and client goals while maintaining compliance standards
  • Participate in client meetings and answer questions about projects when necessary
  • Build strong partnerships with and understand the importance of meeting the needs of internal teams
  • Work on multiple projects concurrently, prioritizing appropriately
  • Collaborate with team to execute project and meet deadlines
  • Emerging ability to assess areas for opportunity and improvement
  • Ensures that work is of the highest quality and instills confidence for clients
  • Begin to think strategically about work and develop an awareness of the work’s impact on business strategy

Requirements:

  • PhD in life sciences, MD, or PharmD
  • At least 1 year of work experience in an agency, the pharmaceutical industry, or a related scientific or medical writing position
  • Working knowledge of digital marketing
  • Commitment to ethical and transparent data dissemination standards
  • Demonstrated ability to work collaboratively in a dynamic team environment
  • Excellent interpersonal, organization, verbal, and written communication skills
  • Excellent quantitative and analytical skills and ability to synthesize complex or diverse information
  • Excellent problem-solving skills
  • Strong attention to detail and listening skills
  • Ability to meet tight deadlines and have excellent time management skills
  • Highly proficient with MS Office (Word, Excel, PowerPoint, Outlook), Adobe, Google or similar calendar system

Nice to have:

  • At least 1 year of experience as an oncology (solid tumors and/or hematologic malignancies) medical writer
  • Preference will be given for experience in hematologic or solid tumor oncology
  • Familiarity with EndNote or other reference management software and publication database (ie, DataVision)
  • Proficient in PubMed or other scientific/medical search websites
What we offer:
  • 100% remote environment with opportunities for local meet-ups
  • Positive, diverse, and supportive culture
  • Investment in you with opportunities for professional growth and personal development through Vaniam Group University
  • Health benefits – medical, dental, vision
  • Generous parental leave benefit
  • Focused on your financial future with a 401(k) Plan and company match
  • Work-Life Balance and Flexibility
  • Flexible Time Off policy for rest and relaxation
  • Volunteer Time Off for community involvement
  • Emphasis on Personal Wellness
  • Virtual workout classes
  • Discounts on tickets, events, hotels, child care, groceries, etc.
  • Employee Assistance Programs

Additional Information:

Job Posted:
December 25, 2025

Employment Type:
Fulltime
Work Type:
Remote work
Job Link Share:

Looking for more opportunities? Search for other job offers that match your skills and interests.

Briefcase Icon

Similar Jobs for Medical Writer, Scientific Communications

Quality Assurance Specialist, Medical Communications

Location
Location
India
Salary
Salary:
Not provided
parexel.com Logo
Parexel
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Experienced Medical Writer (1-2 years)
  • Scientific background and degree (PharmD, MD, PhD or Masters)
  • Knowledge of IT and digital solutions
  • Strong attention to detail and accuracy
  • Ability to manage and prioritize multiple, detailed activities
  • Results-orientated with fast and focused execution
  • Good communication, coordination and time management skills
  • Ability to work within a team or across multiple teams (including remotely) as well as independently
  • Fluent in oral and written English with high level of communication skills
  • Values teamwork, collaboration, and innovation
Job Responsibility
Job Responsibility
  • Cross check scientific information against cited references and ensure medical accuracy (fact check)
  • Ensure consistency with product label where applicable
  • Verify presence of essential information
  • Correct interpretation of scientific data from reference/sources
  • Alignment/formatting of content as per style guides/journal guidelines/congress guidelines
  • Ensure consistency of scientific content across different sections (including text, figures, tables)
  • Accurate bibliography/in-text citation and alignment of figures/graphs as per branding guidelines
  • Confirm that every sentence is source annotated, and each source annotation matches with respective reference and vice versa
  • Ensure that information is presented in a neutral manner without any interpretations and/or author’s conclusion
  • Track work and communicate with client team on job reviews, prioritization etc., through emails and teleconferencing if needed
Read More
Arrow Right

Medical Writer

We are currently looking for a Medical Writer or Senior Medical Writer to be at ...
Location
Location
United Kingdom , Manchester / Macclesfield / London
Salary
Salary:
Not provided
bioscriptgroup.com Logo
Bioscript Group
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Minimum 15 months medical writing experience in an MedComms agency
  • Evident writing skills and a passion for communicating complex ideas backed up with strong customer focus
  • Meticulous attention to detail and the ability to distil complex information for diverse audiences
  • A proactive approach to learning and staying informed about industry trends
  • Enthusiasm for working in a collaborative and dynamic environment
Job Responsibility
Job Responsibility
  • Translating complex scientific data into clear, concise, and accessible content
  • Collaborating with cross-functional teams to create compelling narratives to push the boundaries of medical science
  • Ensuring adherence to industry guidelines and regulatory standards
  • Conducting thorough research to stay abreast of the latest medical advancements
  • Developing educational materials and promotional content that help to bring the next generation of medicines to patients around the world
What we offer
What we offer
  • 25 days holiday + bank holidays + winter shutdown + holiday purchase scheme
  • Enhanced sick and compassionate leave
  • Enhanced maternity, paternity & adoption leave
  • Birthday charity donation to a charity of your choice
  • Bonus Day off to be spent giving back to the community
  • Life Insurance and Critical Illness cover
  • Private Medical (Vitality for UK based colleagues)
  • Health cash plan or wellbeing allowance
  • International Employee Assistance Program
Read More
Arrow Right

Medical Writer

The healthcare industry requires that we abide by regulations from all around th...
Location
Location
Malta , Marsa
Salary
Salary:
Not provided
https://www.baxter.com/ Logo
Baxter
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • BS or MS in scientific or clinical discipline with excellent writing skills
  • 2 years of on-the-job experience in scientific/medical writing (e.g., clinical trial and regulatory documents) preferred but not mandatory
  • Knowledge of computer software Microsoft Word and Adobe Acrobat products
  • Microsoft Project and Visio are a plus
  • Experience in scientific and/or medical writing
  • Experience in the analytical evaluation of scientific data and written or oral presentation in a logical, clear, concise manner
  • Strong organizational skills and meticulous attention to detail
  • Familiarity with clinical trial-related and regulatory clinical submission templates and documents
  • Apply global regulatory authority regulations and/or guidance
  • Manage multiple projects with competing priorities
Job Responsibility
Job Responsibility
  • Develops high quality clinical documents ensuring scientific excellence and regulatory compliance
  • Writing, interpreting and summarizing clinical and non-clinical data
  • Compiling information and ensuring delivery within timelines
  • Ensure compliance of clinical documents with Baxter procedures, national and international regulatory requirements and guidelines
  • Collaborate with cross-functional team members and serve as MW representative at study team meetings
  • Prepare document timelines, with guidance from manager
  • Develop knowledge of one or more Baxter therapeutic areas
Read More
Arrow Right

Medical Writer

We are looking for individuals to write and edit clinical documents to support r...
Location
Location
Malta , Marsa
Salary
Salary:
Not provided
https://www.baxter.com/ Logo
Baxter
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • BS or MS in scientific or clinical discipline with excellent writing skills
  • 2 years of on-the-job experience in scientific/medical writing preferred but not mandatory
  • knowledge of computer software Microsoft Word and Adobe Acrobat products
  • Microsoft Project and Visio are a plus
  • experience in scientific and/or medical writing
  • experience in the analytical evaluation of scientific data and written or oral presentation in a logical, clear, concise manner
  • strong organizational skills and meticulous attention to detail
  • familiarity with clinical trial-related and regulatory clinical submission templates and documents
  • apply global regulatory authority regulations and/or guidance
  • manage multiple projects with competing priorities
Job Responsibility
Job Responsibility
  • Develop high quality clinical documents ensuring scientific excellence and regulatory compliance
  • write, interpret and summarize clinical and non-clinical data
  • compile information and ensure delivery within timelines
  • ensure compliance of clinical documents with Baxter procedures, national and international regulatory requirements and guidelines
  • collaborate with cross functional team members and serve as MW representative at study team meetings
  • prepare document timelines, with guidance from manager, as needed
  • develop knowledge of one or more Baxter therapeutic areas.
Read More
Arrow Right

Scientific Medical Writer

We are seeking a Scientific Writer to serve as a critical bridge between our Res...
Location
Location
Denmark , Københavns Kommune
Salary
Salary:
Not provided
life-science-talent-solutions.dk Logo
Life Science Talent
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • PhD in life sciences, biomedical sciences, pharmacology, immunology, hematology, or related field
  • Demonstrated experience in scientific writing, including peer-reviewed publications as first author or significant contributor
  • Strong understanding of clinical drug development processes and regulatory requirements
  • Excellent written and verbal communication skills with the ability to translate complex scientific concepts for diverse audiences
  • Meticulous attention to detail and commitment to scientific accuracy
  • Strong organizational skills and ability to manage multiple projects simultaneously
  • Proven ability to work collaboratively in a fast-paced, team-oriented environment
Job Responsibility
Job Responsibility
  • Lead the preparation of scientific manuscripts for peer-reviewed publications, demonstrating our research and preclinical findings
  • Lead the preparation of patent filings
  • Develop and write regulatory documentation including: Technical reports, Investigator's Brochures and briefing documents
  • Investigational New Drug (IND) applications and Clinical Trial Applications (CTAs)
  • Regulatory responses and agency communications
  • Create high-quality abstracts, posters, and presentations for scientific conferences
  • Collaborate with Medical Affairs to develop scientifically accurate medical communications materials
  • Prepare scientific brochures, data summaries, and disease-state educational content
  • Support the creation of materials for advisory boards and key opinion leader (KOL) engagements
  • Contribute to medical information responses and scientific exchange materials
What we offer
What we offer
  • Opportunity to make a meaningful impact on patients living with rare bleeding disorders who have few or no treatment options
  • Collaborative, mission-driven culture with a commitment to scientific excellence
  • Work at the forefront of innovation in bleeding disorder therapeutics
  • Professional development opportunities and growth within a rapidly expanding organization
  • Fulltime
Read More
Arrow Right

Senior Medical Writer

The Senior Medical Writer: 1) writes original content for publications activitie...
Location
Location
United States , West Chester
Salary
Salary:
Not provided
synchronygroup.com Logo
Synchrony Group
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • PhD, PharmD, or MD
  • Minimum of 3 years’ experience in medical communications
  • Substantial professional medical writing experience in a wide variety of communication formats
  • Ability to work independently on assigned projects
  • Excellent attention to detail and high degree of scientific and medical accuracy
  • Ability to manage outcomes to win-win resolution
  • Ability to identify key issues and to creatively and strategically overcome challenges or obstacles
  • High level of integrity, ethics, confidentiality, and accountability
  • Sound analytical thinking, planning, prioritization, and execution skills with an ability to multitask
  • Well-developed professional communication skills, including written and interpersonal
Job Responsibility
Job Responsibility
  • Demonstrate a command of assigned therapeutic areas and expertise with assigned products
  • Write original content for publication/communication activities (primary and review manuscripts, abstracts, posters), slide presentations, meeting summaries, and other materials for HCP and internal audiences
  • Prepare materials according to internal writing guidelines and other applicable guidelines (eg, client-specific style guidelines, compliance best practices, journal style guidelines)
  • Follow all internal processes and procedures with regard to workflow, development of deliverables, and adherence to industry best practices, including GPP3
  • Demonstrate the flexibility/adaptability necessary to function on different therapeutic teams as needed
  • Interpret and apply clinical data
  • Maintain a proactive approach on initiatives for existing and prospective clients
  • Work in conjunction with team members to manage workload and develop and adhere to logical and attainable timelines for project completion
  • Attend team meetings to provide input and aid in troubleshooting/problem-solving
  • Efficiently and accurately collate and incorporate author/client comments
What we offer
What we offer
  • Competitive salaries
  • Generous paid time off
  • Excellent health insurance
  • Family leave
  • 401(k) plan with employer matching
  • Fulltime
Read More
Arrow Right

Associate Medical Writer

EMJ is looking for an Associate Medical Writer to join our growing team. This is...
Location
Location
United Kingdom , London
Salary
Salary:
35000.00 GBP / Year
emjreviews.com Logo
EMJ
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Degree (MSc or PhD) in a scientific, medical, or healthcare-related field
  • Strong interest in medical writing or healthcare communications
  • Excellent written and verbal communication skills, with strong attention to detail
  • Organised, proactive, and able to manage multiple tasks with support
  • Eager to learn, take feedback onboard, and develop skills quickly
  • Basic understanding of scientific research and interest in the pharmaceutical/healthcare industry
Job Responsibility
Job Responsibility
  • Support the creation of high-quality scientific content, including symposium reviews, eLearning modules, and KOL interviews
  • Conduct literature research and summarise complex scientific data into clear, engaging content
  • Assist with the development of educational materials, including needs assessments and gap analyses
  • Work closely with senior writers and the wider team to deliver projects on time and to a high standard
  • Contribute to multimedia content such as webinars, podcasts, and infographics
  • Attend (or support coverage of) key medical congresses and help identify important scientific insights
  • Ensure all work aligns with ethical, legal, and regulatory standards
  • Incorporate feedback from internal stakeholders and clients to continuously improve work
What we offer
What we offer
  • Opportunities for progression
  • Bupa medical cashback after passing probation
  • Aviva private medical insurance after one year
  • Bike to Work scheme
  • 25 days of holiday, plus an extra day for each year of service (up to 30 days)
  • 1.5-Hour Gym Lunch
  • Enhanced maternity leave
  • Summer Ball
  • Christmas celebrations
  • Fulltime
Read More
Arrow Right
New

Freelance Medical Writers (2 Positions)

Our client, a NYC-based pharmaceutical agency, is seeking experienced Freelance ...
Location
Location
United States
Salary
Salary:
Not provided
solomonpage.com Logo
Solomon Page
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Strong background in pharmaceutical sciences, life sciences, or a related field
  • Prior experience in a medical communications or advertising agency environment preferred
  • Experience with scientific writing, referencing, and annotation of clinical content
  • Familiarity with Medical-Legal-Regulatory (MLR) review processes
  • Proven ability to interpret, review, and summarize peer-reviewed medical literature
  • Strong attention to detail with the ability to manage deadlines in a fast-paced environment
Job Responsibility
Job Responsibility
  • Develop, edit, and review high-quality medical and scientific content for pharmaceutical and healthcare communications
  • Annotate, cite, and reference scientific and clinical source materials accurately and consistently
  • Conduct literature reviews and synthesize findings from peer-reviewed medical journals
  • Support Medical-Legal-Regulatory (MLR) review processes, including addressing reviewer feedback and ensuring compliance
  • Collaborate closely with cross-functional teams including account, strategy, creative, and medical affairs
  • Ensure all deliverables meet scientific accuracy, regulatory requirements, and brand guidelines
What we offer
What we offer
  • medical
  • dental
  • 401(k)
  • commuter benefits
  • Fulltime
Read More
Arrow Right