Indegene Inc.
Overview
Title: Director - Medical Communications Date: 22 Sept 2025 Location: NJ, US We are a technology-led healthcare solutions provider. We are driven by our purpose to enable healthcare organizations 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 Indegene is scouting for leaders who can help us write the next chapter of our growth story. We are at the exciting intersection of healthcare and technology and are rapidly growing in a sustainable fashion. We are enabling healthcare organizations be future ready for which we are building new capabilities every day and need employees to build things from scratch for us and take ownership. You will be leading teams and delivering outcomes while working with a purpose-driven organization. We are a passionate team that likes to make a difference with our work in our customers’ lives. We ensure a differentiated career for our employees.
Responsibilities
Objective: Provide strategic scientific leadership and ensure development of accurate, high-quality, and compliant scientific content across multiple communication channels. Collaborate across internal teams (US, Europe & India) and external clients as the key medical expert guiding strategy and execution.
Focus areas: Support an upcoming ADHD launch while providing scientific input for other therapeutic areas and client initiatives; report to the VP Medical Affairs and Head of Medical Strategy.
Scientific Leadership & Strategy: Collaborate with client teams and offshore colleagues to align content strategy, messaging, and delivery; lead the multi-year global medical strategy for the specified product/TA in line with overall product/brand strategy.
Conferences and launches: Work with Medical Affairs teams during congresses, product launches, and data releases; prioritize medical communication deliverables; support publications and medical education activities.
Therapeutic area leadership: Provide leadership in key TAs including neurology, oncology, respiratory, cardiovascular, rare diseases, etc.
Content Development & Review: Research, develop, and review materials for scientific accuracy, context, fair balance, audience suitability, and compliance with quality standards.
Document development: Review and/or develop medical and scientific documents (publications, slide decks, scientific platforms, abstracts, newsletters, posters, videos, infographics, medical information letters, etc.).
Cross-functional collaboration: Participate in meetings for development, review, and maintenance of Medical Affairs deliverables with colleagues; understand review platforms (e.g., Veeva) for analysis and tracking.
Ethics and compliance: Collaborate with Legal, Compliance, and Regulatory to ensure ethical interactions with external stakeholders.
Cross-Functional Collaboration: Partner with internal teams (medical writers, project managers, creative teams) based in India to deliver outputs on time; act as liaison with client stakeholders (Medical Affairs, Legal, Regulatory, Commercial).
Medical insights: Inform advisory boards, 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 areas, processes, and platforms; give clear, actionable feedback to offshore writing teams to ensure accuracy and compliance; adapt to new technologies and platforms in the domain.
Education, Behavioral Competencies and Skills
Medical degree or advanced Life Science degree with experience in the life sciences industry; medical communications agency experience in a scientific/medical role.
Minimum 10+ years in Medical Affairs/Medical Communications within the pharmaceutical industry, including 3+ years in ADHD or related CNS disorders.
Proven track record in publications planning and execution per GPP and ICMJE guidelines.
Familiarity with medical strategy development, KOL engagement, and congress activities.
Experience in launch strategies across major markets.
Experience in the disease area of interest through clinical or biopharmaceutical experience preferred.
CMPP or other medical writing, medical communications, or Medical Affairs certification is an advantage.
Attributes: Strategic thinking; ability to synthesize scientific data into impactful communication; excellent written and verbal communication; strong collaboration and stakeholder management; 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.
Equal Opportunity EQUAL OPPORTUNITY
Indegene is proud to be an Equal Employment Employer and is committed to a 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.
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Title: Director - Medical Communications Date: 22 Sept 2025 Location: NJ, US We are a technology-led healthcare solutions provider. We are driven by our purpose to enable healthcare organizations 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 Indegene is scouting for leaders who can help us write the next chapter of our growth story. We are at the exciting intersection of healthcare and technology and are rapidly growing in a sustainable fashion. We are enabling healthcare organizations be future ready for which we are building new capabilities every day and need employees to build things from scratch for us and take ownership. You will be leading teams and delivering outcomes while working with a purpose-driven organization. We are a passionate team that likes to make a difference with our work in our customers’ lives. We ensure a differentiated career for our employees.
Responsibilities
Objective: Provide strategic scientific leadership and ensure development of accurate, high-quality, and compliant scientific content across multiple communication channels. Collaborate across internal teams (US, Europe & India) and external clients as the key medical expert guiding strategy and execution.
Focus areas: Support an upcoming ADHD launch while providing scientific input for other therapeutic areas and client initiatives; report to the VP Medical Affairs and Head of Medical Strategy.
Scientific Leadership & Strategy: Collaborate with client teams and offshore colleagues to align content strategy, messaging, and delivery; lead the multi-year global medical strategy for the specified product/TA in line with overall product/brand strategy.
Conferences and launches: Work with Medical Affairs teams during congresses, product launches, and data releases; prioritize medical communication deliverables; support publications and medical education activities.
Therapeutic area leadership: Provide leadership in key TAs including neurology, oncology, respiratory, cardiovascular, rare diseases, etc.
Content Development & Review: Research, develop, and review materials for scientific accuracy, context, fair balance, audience suitability, and compliance with quality standards.
Document development: Review and/or develop medical and scientific documents (publications, slide decks, scientific platforms, abstracts, newsletters, posters, videos, infographics, medical information letters, etc.).
Cross-functional collaboration: Participate in meetings for development, review, and maintenance of Medical Affairs deliverables with colleagues; understand review platforms (e.g., Veeva) for analysis and tracking.
Ethics and compliance: Collaborate with Legal, Compliance, and Regulatory to ensure ethical interactions with external stakeholders.
Cross-Functional Collaboration: Partner with internal teams (medical writers, project managers, creative teams) based in India to deliver outputs on time; act as liaison with client stakeholders (Medical Affairs, Legal, Regulatory, Commercial).
Medical insights: Inform advisory boards, 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 areas, processes, and platforms; give clear, actionable feedback to offshore writing teams to ensure accuracy and compliance; adapt to new technologies and platforms in the domain.
Education, Behavioral Competencies and Skills
Medical degree or advanced Life Science degree with experience in the life sciences industry; medical communications agency experience in a scientific/medical role.
Minimum 10+ years in Medical Affairs/Medical Communications within the pharmaceutical industry, including 3+ years in ADHD or related CNS disorders.
Proven track record in publications planning and execution per GPP and ICMJE guidelines.
Familiarity with medical strategy development, KOL engagement, and congress activities.
Experience in launch strategies across major markets.
Experience in the disease area of interest through clinical or biopharmaceutical experience preferred.
CMPP or other medical writing, medical communications, or Medical Affairs certification is an advantage.
Attributes: Strategic thinking; ability to synthesize scientific data into impactful communication; excellent written and verbal communication; strong collaboration and stakeholder management; 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.
Equal Opportunity EQUAL OPPORTUNITY
Indegene is proud to be an Equal Employment Employer and is committed to a 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.
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