Job description

About the role

Inizio Engage works in a long-term partnership with a leading biotechnology organization spanning Commercial, Patient Solutions, and Medical Affairs functions. This role is centered on developing high-quality medical information content across multiple channels for therapeutic areas, ensuring communications are scientifically sound, meaningful, and suitable for patients, healthcare professionals, and access stakeholders.

This opportunity offers the chance to join Inizio Engage and support a major biotechnology client in a hybrid setup based in Titusville, New Jersey, with on-site presence required three days each week.

What you will do

Develop, co-develop, and quality-check medical content for patients, healthcare professionals, and payers so that the material remains scientifically robust, balanced, and effective. This includes field medical slides for Medical Science Liaisons and Managed Care Liaisons, as well as standard and more complex medical information responses.
Monitor repeated inquiries and determine when new standard responses should be created.
As required, conduct medical reviews for scientific accuracy and contribute to the creation and use of scientific and promotional materials in line with approved client procedures, including PRC and RDC workflows.
Work closely with client Medical Content Strategy Leads and MI leadership to identify learning needs for Medical Information, Communications teams, internal partners, and external vendors.
Draft, review, edit, and deliver medical training content when needed.
Prepare US medical information responses by interpreting and summarizing complex scientific literature in a clear, balanced, compliant, and clinically useful format for healthcare decision-making.
Maintain a strong product-response medical information database and support launch readiness planning that aligns with customer scientific needs.
Act as the therapeutic area subject matter expert while keeping product and disease knowledge current and detailed.
Carry out continuous literature reviews and organize complex scientific data into structured, usable formats.
Offer clinical direction and medical information support to help resolve escalated medical or access questions coming through the contact center.
Use internal scientific narratives and creative data visualization approaches to build medical resources and tools that improve scientific engagement.
Review difficult or escalated medical information cases.
Assess derivative content and confirm it stays aligned with medical information responses and approved review processes.
Provide stakeholders with practical insights and recommendations based on therapeutic area and product expertise.
Create or refresh reference documents and data-on-file summaries.
Support quality improvement and training activities for team members in partnership with leadership and, where relevant, the client.

Requirements

An advanced degree in clinical or scientific study, such as a PhD, PharmD, or an equivalent qualification.
At least 3 years of relevant experience in medical communications, with neurology exposure preferred.
At least 3 years of direct medical information experience and/or related medical affairs experience in the pharmaceutical industry, clinical environment, or a comparable setting.
Strong verbal, written, and listening communication abilities.
Comfortable using Google Workspace and Office 365.
Able to work effectively on your own as well as in team settings.
Capable of using computer hardware and software smoothly in day-to-day work.

Compensation and benefits

The base salary range for this position is $88,000 to $163,000 per year, with final pay determined by experience, skills, internal equity, and business requirements.

Benefits include medical, dental, and vision coverage; accrued paid time off; a 401(k) plan with company match; disability and life insurance; paid maternity and paternity leave; company-paid holidays; recognition programs; contests and awards; learning and leadership development opportunities; and support for career advancement.

Recognition and culture

The company highlights an employee-focused culture and has been recognized as a Best Place to Work in BioPharma in 2022, 2023, and 2025, as well as a Certified Great Place to Work in 2021, 2023, 2025, and 2026. It also emphasizes collaboration, appreciation of employee ideas, and meaningful work that contributes to healthcare outcomes.

Equal opportunity and hiring policies

Inizio Engage is an equal opportunity employer and considers all qualified candidates without discrimination based on protected characteristics under applicable law. Reasonable accommodations are available in line with legal requirements.

The company follows fair chance hiring practices where allowed by law and may condition offers on a background check. Information from that check will be assessed only as permitted and relevant to the role.

Artificial intelligence policy for interviews

Candidates are expected to complete interview activities without using artificial intelligence tools or outside help unless prior authorization has been granted by Inizio Engage or accommodation is required by law. This includes using generative AI to create, edit, or guide responses in real time. Candidates may be asked to confirm adherence to this rule, and violations can lead to removal from consideration. Requests for reasonable accommodation may be directed to the Talent Acquisition team.

About Inizio Engage

Inizio Engage is a strategic commercial and creative partner focused on healthcare engagement. The company combines local market knowledge with a global team and capabilities in data, science, and technology to create tailored engagement solutions that help clients improve how they connect with patients, payers, healthcare professionals, and providers. Its mission is to help improve lives by enabling better access to medicines, knowledge, and support.

The organization states core values centered on empowerment, teamwork, challenge, curiosity, and doing the right thing.

Medical Writer

Where you'll work