Indegene: Publications Lead, Medical Affairs (Dermatology)
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Trilogy Writing and Consulting
Princeton, NJ, US
Summary
The Publications Lead will develop and execute scientific publication strategies for the Dermatology therapeutic area while ensuring high-quality, compliant content. They will act as a key liaison between internal cross-functional teams and external clients to manage medical communication deliverables.
Job Description
We are a technology-led healthcare solutions provider. We are driven by our purpose to enable healthcare organizations to be future ready. We offer accelerated, global growth opportunities for talent that’s bold, industrious and nimble. With Indegene, you gain a unique career experience that celebrates entrepreneurship, and is guided by passion, innovation, collaboration and empathy. To explore exciting opportunities at the convergence of healthcare and technology, check out www.careers.indegene.com
What if we told you that you can move to an exciting role in an entrepreneurial organization without the usual risks associated with it?
We understand that you are looking for growth in your career at this point and we would love for you to join us in our journey and grow with us. At Indegene, our roles come with the excitement you require at this stage of your career while providing the reliability you seek. We believe in creating leaders of tomorrow and mentor our team to help them grow and nurture them as people managers and account managers.
We are a rapidly growing global organization and are scouting for the best talent for this phase of growth. With us, you are at the intersection of two of the most exciting industries: healthcare and technology. We offer global opportunities with fast-track careers while you work with a team that is fueled by purpose. This combination will lead to a truly differentiated experience for you.
If this excites you, then apply below.
Position: Publications Lead
Location: US (remote) - must be based in US
We are seeking an experienced Publications Lead with experience in Dermatology therapeutic area (TA) to join our Medical Affairs team. This individual will provide publications strategy, writing and review support and ensure the development of accurate, high-quality, and compliant scientific content across multiple communication channels. The role requires extensive cross-functional collaboration with internal teams (based in US, Europe & India) and external clients, serving as the key medical expert to guide strategy and execution.
While the immediate focus will be on supporting publications related to Dermatology TA, this role will also extend to other TAs, providing scientific expertise and strategic input for a broad range of client initiatives. The position will report to the Director of Publications.
KEY RESPONSIBILITIES
Scientific Strategy
- Collaborate closely with client teams and offshore colleagues to ensure alignment on overall content strategy, scientific narrative, and messaging flow. Act as a key liaison between internal and client teams, ensuring seamless communication, alignment, and delivery of high-quality content.
- Serve as the primary medical/scientific expert to lead the development and execution of dermatology TA/product publications, appropriately aligned with overall product/brand strategy.
- Work with pharmaceutical Medical Affairs teams during congresses, product launches, and key data releases, coordinate and lead on prioritization of medical communication deliverables. Support strategic planning of publications, medical education, and other non-promotional scientific activities.
- Provide therapeutic area leadership in key TAs including (but not restricted to) dermatology, Women’s health, neurology, oncology, respiratory, cardiovascular, rare diseases etc.
Content Development & Review
- Research, develop, and review materials to ensure scientific accuracy, appropriate contextualization, fair balance, audience suitability of content, and compliance with quality standards.
- Review and/or develop medical and scientific documents, including (but not limited to) publications (abstracts, posters/oral presentations, and manuscripts of all types), slide decks, scientific platforms, medical meeting materials etc.
- Participate in meetings for development, review, and maintenance of key Medical Affairs deliverables in collaboration with Medical Affairs colleagues.
- Understanding of Datavision/iEnvision platforms and tracking of publications.
- Collaborate with Legal, Compliance and Regulatory to ensure proper and ethical interactions between Global Medical Affairs personnel and external stakeholders
Cross-Functional Collaboration
- Partner with internal teams (medical writers, project managers, creative team) based in India to deliver high-quality outputs within timelines.
- Act as a key liaison with client stakeholders, including Medical Affairs, Legal, Regulatory, and Commercial teams.
- Provide medical insights to inform advisory boards, symposiums, KOL engagement strategies, and pre-launch/launch initiatives.
Training & Knowledge Sharing
- Provide training, mentoring, and consulting support to internal and cross functional teams on therapy area, processes, platforms etc.
- Provide clear, actionable feedback to the offshore writing teams to ensure scientific accuracy, consistency, and compliance across deliverables.
- Ability to adapt to latest trends in application of newer technologies and platforms related to the domain to build competencies.
EDUCATION, BEHAVIORAL COMPETENCIES AND SKILLS:
- A medical degree/advanced Life Science degree with prior experience of working with or within the life sciences industry; medical communications agency in scientific/medical role
- Minimum 5+ years of experience in Medical Affairs/Publications within the pharmaceutical industry, including 3+ years in Dermatology.
- Proven track record in publications planning and execution as per GPP, ICMJE, and EQUATOR network guidelines.
- Familiarity with medical strategy development, KOL engagement, and congress activities.
- Experience in the disease area of interest through clinical experience or biopharmaceutical experience is preferred
- CMPP or other medical writing, medical communications, or Medical Affairs certification would be an advantage
Attributes:
- Strategic thinking and ability to synthesize scientific and clinical data into impactful communication
- Excellent written and verbal communication skills, with the ability to convey complex data with clarity
- Strong collaboration and stakeholder management skills across diverse functions.
- Ability to work in a fast-paced, matrix environment with multiple priorities.
- Detail-oriented with a commitment to quality and compliance.
- Understanding of Indian Contexts/Ecosystem
Compensation: $120,000 - $140,000USD
EQUAL OPPORTUNITY
Indegene is proud to be an Equal Employment Employer and is committed to the culture of Inclusion and Diversity. We do not discriminate on the basis of race, religion, sex, color, age, national origin, pregnancy, sexual orientation, physical ability, or any other characteristics. All employment decisions, from hiring to separation, will be based on business requirements, candidate’s merit and qualifications.
We are an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, gender identity, sexual orientation, disability status, protected veteran status, or any other characteristics.
At Trilogy, medical writing is our passion. As specialists in clinical regulatory documentation, we provide a service that is more than just writing. Our writers are integral parts of our clients’ teams: proactively planning, coordinating and writing their clinical documents to meet timelines, with a readability that reduces the time for review and approval. We have been helping pharmaceutical companies and clinical research organizations of all sizes, worldwide, to streamline their documentation processes for over 18 years – either as support on a one-off document or the entire clinical development program.
We provide our clients with a constructive advice on their projects: we guide our clients’ teams through the writing process and ask them the right questions in order to produce documents that communicate effectively. Our writers are trained to understand that our job is not to produce a data dump: it is to think about the data available and work with the team to pull out the messages and present them as clearly as possible, so that a reviewer can quickly find the information they are looking for and easily understand the story to be told. Our approach to writing clinical documentation ideally results in a minimum of clarifying questions from reviewers, speeding the process of review and ultimately leading to faster approval.
Trilogy currently has more than 80 writers, who are located in 3 offices: Frankfurt in Germany (HQ), London in the UK, and Durham, North Carolina in the US.
Founded
2002
Company size
51-200 employees
Industry
Writing and Editing
Org type
Privately Held
Headquarters
Frankfurt
At Trilogy, medical writing is our passion. As specialists in clinical regulatory documentation, we provide a service that is more than just writing. Our writers are integral parts of our clients’ teams: proactively planning, coordinating and writing their clinical documents to meet timelines, with a readability that reduces the time for review and approval. We have been helping pharmaceutical companies and clinical research organizations of all sizes, worldwide, to streamline their documentation processes for over 18 years – either as support on a one-off document or the entire clinical development program.
We provide our clients with a constructive advice on their projects: we guide our clients’ teams through the writing process and ask them the right questions in order to produce documents that communicate effectively. Our writers are trained to understand that our job is not to produce a data dump: it is to think about the data available and work with the team to pull out the messages and present them as clearly as possible, so that a reviewer can quickly find the information they are looking for and easily understand the story to be told. Our approach to writing clinical documentation ideally results in a minimum of clarifying questions from reviewers, speeding the process of review and ultimately leading to faster approval.
Trilogy currently has more than 80 writers, who are located in 3 offices: Frankfurt in Germany (HQ), London in the UK, and Durham, North Carolina in the US.
Founded
2002
Company size
51-200 employees
Industry
Writing and Editing
Org type
Privately Held
Headquarters
Frankfurt