Senior Medical Writer Publications
Senior Medical Writer Publications
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Job Description
AIM OF THE POSITION
The Senior Medical Publications Writer is an expert in publication writing and performs work independently. Reporting to the VP Clinical Development the Senior Medical Publications Writer will play a pivotal role in the development and of publication plans and lead scientific communication efforts by developing highquality evidencebased publications and congress materials ensuring alignment in company objectives and adherence to good publication practices. This role will work crossfunctionally with Medical and Clinical Affairs Commercial and with external investigators.
POSITION WITHIN THE ORGANIZATION
1. Reports to Vice President Clinical Development
2. Cooperates with all departments
3. Participates in:
Crossfunctional projects and meetings
ESSENTIAL DUTIES AND RESPONSIBILITIES
Publication Planning and :
Lead the development and of scientific publication plans for clinical trials realworld evidence studies and translational research findings within preestablished timelines
Develop highimpact manuscripts abstracts posters and presentations for peerreviewed journals and scientific congresses in collaboration with crossfunctional teams.
Ensure alignment of publication strategies with the companys medical and clinical objectives supporting evidence generation and dissemination initiatives
Maintain a thorough understanding of the competitive landscape identifying key areas for publication and differentiation in the oncology space.
Participate in and assist with meetings and discussions with crossfunctional teams to develop a publication strategy and ensure all stakeholders are involved in the publication process.
Scientific Writing and Data Interpretation:
Translate complex clinical and scientific data into clear compelling and scientifically accurate publications tailored to diverse audiences including oncologists researchers and regulatory bodies.
Collaborate with biostatisticians and data scientists to analyze and interpret clinical and realworld evidence ensuring statistical accuracy and clinical relevance.
Perform literature reviews and competitive analyses to support publication development ensuring manuscripts are well contextualized within the existing body of evidence.
Assist in the development of scientific communication materials such as educational slide decks white papers and executive summaries to support internal and external stakeholders.
Project and Publication Management:
Manage multiple concurrent publication projects ensuring timelines and deliverables are met with scientific rigor and operational excellence.
Oversee the manuscript review process coordinating with authors internal teams and journal editors to ensure timely submission and publication
Helps coordinate publications/presentations/congress events with marketing for appropriate visibility (i.e. press releases poster and presentation summaries)
Maintain publication libraries reference databases and literature repositories for streamlined access and organization.
Compliance and Ethical Standards:
Ensure publications comply with AMA writing style Good Publication Practices (GPP) ICMJE guidelines and Agendiaspecific SOPs.
Participate in postmarket surveillance efforts by evaluating new literature summarizing emerging data and contributing to updates on clinical and scientific positioning.
CrossFunctional and External Collaboration:
Work closely with internal stakeholders (Medical Affairs Clinical Development R&D and Marketing) and external authors (Key Opinion Leaders investigators and collaborators) to develop impactful scientific communications
Partner with the Medical Science Liaison (MSL) team Marketing and other stakeholders to ensure publications align with field insights and unmet medical needs
The above listing represents the general duties considered essential functions of the job and is not to be considered a detailed description of all the work requirements that may be inherent in the position.
KEY CONTACTS
Internal
o Medical and Clinical Affairs teams Marketing and R&D
External
o Works closely with external collaborators (i.e. KOLs investigators physicians and researchers)
EDUCATION AND EXPERIENCE REQUIREMENTS
EDUCATION
PhD PharmD or MD in Biomedical Sciences Oncology Molecular Biology or a related field.
Masters degree with significant publication experience may be considered
EXPERIENCE
5 years of experience in medical writing publication planning or scientific communications within oncology diagnostics or the pharmaceutical/biotech industry.
Proven track record of firstauthorship in peerreviewed journals and scientific congress presentations.
Strong understanding of oncology research biomarkerdriven therapies and precision medicine approaches.
Experience working with realworld evidence translational research and clinical trial publications is highly desirable.
Proficiency with publication management software reference management tools (EndNote Mendeley) and literature databases (PubMed)
KNOWLEDGE SKILLS AND ABILITIES (KSAS)
Specific Knowledge Required:
Knowledge: Comprehension of a body of information acquired by experience or study.
Skill: A present observable competence to perform a learned activity.
Ability: Competence to perform an observable behavior.
Expertlevel scientific writing and editing skills with the ability to synthesize complex data into compelling narratives.
Strong analytical skills with a deep understanding of biostatistics data visualization and clinical study design.
Demonstrated ability to manage multiple highpriority projects in a fastpaced environment.
Exceptional stakeholder engagement and project management skills with experience leading crossfunctional teams.
High level of attention to detail scientific integrity and commitment to excellence in publication development.
Proficiency in the following tools:
o Data Visualization software (i.e. Adobe Illustrator PowerPoint Microsoft Excel GraphPad Prism)
o Manuscript development tools (Microsoft Office Word).
o Reference managers (Endnote Mendeley)
Knowledge and experience in performing data analysis a significant plus
Preferably experience with reference management software such as EndNote Mendeley
BEHAVIOURAL COMPETENCIES/DESIRED SKILLS
o Ability to multitask
o Result and customer orientation
o Selforganization
o Quality oriented and results focused
o Initiative
o Flexibility
o Can doattitude
PRIVACY NOTICE: To review the California privacy notice click here: https://agendia/privacypolicy/
Employees must not be classified as an excluded individual who is prohibited from participation in any Federal health care program.
WORKING ENVIRONMENT
Establishes ADA (Americans with Disabilities Act) requirements
ENVIRONMENT/SAFETY/WORK CONDITIONS
Working conditions (inside or outside the office).
General office environment. Adheres to Department Specific Safety Guidelines.
TRAVEL
o Ability to drive/fly domestically up to 10
OTHER DUTIES
Other duties as required.
Required Experience:
Senior IC
Employment Type
Full-Time
