Senior Scientist, Scientific Communications

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Senior Scientist, Scientific Communications, york col-narrow-left
Client: Genesis Research Group
Location: Job Category: Other
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EU work permit required: Yes
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Job Views: 4
Posted: 31.05.2025
Expiry Date: 15.07.2025
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Job Description: Genesis is one of the leading evidence generation consultancies providing agile, tech-enabled real-world evidence (RWE), as well as health economics and outcomes research (HEOR) solutions to clients in the pharmaceutical, biotech, and medical device industries. Since 2009, we’ve partnered with our clients to develop impactful evidence across the product lifecycle to optimize market access for novel healthcare innovations and satisfy regulatory, provider, and payer evidence requirements. Genesis is database agnostic, regularly working across many structured and unstructured real-world data sources. As a company, we deliver services across many RWE and HEOR applications and a wide range of therapeutic areas with an emphasis on uncompromising quality, scientific rigor, and flexible solutions.
The Scientific Communication team and this position:
Our SciComm team consists is seeking a skilled scientist/medical writer to join our dynamic team.
The successful candidate will be responsible for drafting, revising, and editing high-quality scientific deliverables including manuscripts, abstracts, posters, and slide decks. These deliverables will support projects grounded in real-world evidence (RWE), health economics and outcomes research (HEOR), and market access strategy.
Candidates should be prepared to demonstrate enthusiasm for good writing, excellent project management skills, attention to detail, and a genuine willingness to learn. Candidates should be able to communicate clearly and effectively in written English, producing well-organized, accurate, and audience-tailored content.
This position will report to the Senior Director, Value and Scientific Communications.
Accountabilities within this role:
Draft, revise, and finalize scientific materials, including:
Abstracts for scientific conferences
Scientific posters and slide decks for podium presentations
Tables, figures, and data visualizations
Demonstrate an ability to articulate complex information clearly and concisely
Correctly evaluate and interpret source documents and demonstrate an ability to develop appropriate tables and figures
Provide copy editing, proofreading, and quality control reviews for other writers and researchers
Collaborate with internal researchers and client teams to ensure scientific accuracy using protocols, study reports, results tables, and other source documents to develop outlines and draft documents
Remotely participate in client-facing project meetings as needed
Methodically incorporate author and reviewer comments to improve the accuracy and clarity of the documents
Address, revise, and clarify conflicting and/or ambiguous comments from authors and reviewers
Perform relevant online searches of the clinical literature and summarize the findings
Coordinate and complete journal/abstract submissions that adhere to submission guidelines and client templates
Work across therapy areas to learn about different types of studies and methods
Develop familiarity with current industry practices, regulatory requirements, and guidelines that affect medical writing
Share ideas for process improvement across the organization
Demonstrate an interest in monitoring assigned projects and managing own workload, taking ownership, and anticipating capacity issues and potential solutions
Maintain compliance with publication policies and procedures, including confidentiality, Quality Management System, secure file transfer, copyright law, and privacy protection
Participate in training opportunities to enhance relevant skills and share learnings with the larger team
Support and encourage junior staff members involved in writing projects
Contribute to internal thought leadership projects
Qualifications:
Master’s or other advanced degree in a life science, public health, or health economics-related field
More than 2 years of experience in a technical writing role as a professional or student
Strong attention to detail, clarity, and scientific accuracy
Ability to work independently in a deadline-driven environment
Effective interpersonal/verbal communications skills
Proficiency in Microsoft Office (Word, PowerPoint, Excel)
Experience with GraphPad Prism and Adobe tools (Illustrator, InDesign, Acrobat Pro) is a plus
Proficiency in EndNote
Proven experience writing for the pharmaceutical industry, public health, RWE, epidemiology, and/or HEOR is strongly preferred
Graphic design skills are preferred
Compensation:
Performance-related bonus
Flexible PTO and numerous company holidays, including the last week of the year
Genesis Research is an equal opportunity employer.

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