Inizio Engage

Medical Writer

Inizio Engage

Princeton, Indiana, United States (Hybrid) · Full Time

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Experience
3+ yrs
Salary
USD 88,000 – USD 163,000 / year
Openings
1
Posted
5 hours ago
Work mode
Hybrid
Education
PhD, PharmD, or equivalent advanced clinical/science degree
Eligibility
Qualified candidates with an advanced clinical or science degree and at least 3 years of relevant experience in medical communications, medical information, medical affairs, or a clinical/pharmaceutical setting may apply. Neurology experience is preferred but not mandatory.
Resume
Required to apply

Where you'll work

Job description

Role Overview

Inizio Engage partners with a major biotechnology organization supporting Commercial, Patient Solutions, and Medical Affairs work. This role is centered on developing scientifically sound medical information content across several channels and therapeutic areas for patients, healthcare professionals, and access stakeholders.

The position is a hybrid role based in Titusville, NJ, with on-site work required three days per week.

What You’ll Do

  • Develop or co-develop, assess, and refine medical content for patients, HCPs, and payers so that the material remains accurate, balanced, and effective. This includes field medical materials for Medical Science Liaisons and Managed Care Liaisons, along with standard and more complex medical information responses.
  • Monitor repeated inquiries and spot opportunities to create new standard response documents.
  • When required, conduct scientific review for accuracy and contribute to the creation and use of scientific or promotional materials in line with approved client procedures and review pathways such as PRC and RDC, while working closely with client Medical Content Strategy Leads and MI leadership to identify training needs for MI, Communications, internal teams, and external vendors.
  • Draft, assess, edit, and provide medical content for training-related use cases as needed.
  • Prepare and review US MI responses by reviewing complex scientific publications and summarizing them in a clear, accurate, fair-balanced, concise, and compliant way to support clinical decision-making.
  • Build and maintain a strong product response MI database, including launch preparedness plans that address customer scientific needs.
  • Act as a therapeutic area specialist and retain strong depth of knowledge about the product and disease area.
  • Continuously review scientific literature and pull out complex data, then organize it into a usable structure.
  • Offer clinical direction and medical information support to help resolve escalated medical or access-related questions from the contact center.
  • Use internal scientific narratives and creative data visualization methods to build medical resources and tools that improve scientific engagement.
  • Handle review of difficult or escalated MI cases.
  • Examine derivative content and confirm it stays aligned with MI responses and the relevant review and approval workflow.
  • Share practical insights and recommendations with stakeholders based on product and therapeutic-area expertise.
  • Create or refresh reference materials and data-on-file summaries.
  • Support quality and training efforts for team members in collaboration with leadership and, where appropriate, the client.

What Makes This Opportunity Attractive

  • Competitive compensation aligned with experience, expertise, and impact.
  • Full benefits package including medical, dental, and vision coverage; accrued paid time off; 401(k) with company match; disability and life insurance; and paid maternity and paternity leave.
  • Company-paid holidays.
  • Recognition programs, contests, and awards.
  • Learning, leadership development, and advancement support.
  • A collaborative environment where employee ideas are valued.

Requirements

  • An advanced clinical or science degree such as a PhD, PharmD, or a comparable qualification.
  • At least 3 years of relevant medical communications experience, with neurology experience preferred.
  • At least 3 years of direct medical information experience and/or relevant medical affairs experience in pharma, a clinical setting, or a similar background.
  • Strong speaking, writing, and listening skills.
  • Comfort working independently as well as in a team setting.
  • Proficiency with Google Workspace and Office 365.
  • Ability to use computer hardware and software effectively on a daily basis.

Additional Information

The base salary range for this position is $88,000 to $163,000 per year. Final pay will depend on experience, skills, internal equity, and business needs.

Inizio Engage is an equal opportunity employer and considers all qualified applicants without regard to protected characteristics under applicable law. Reasonable accommodations are available in line with legal requirements.

The company follows fair chance hiring practices and may consider qualified applicants regardless of criminal history where allowed by law. Employment offers may be subject to a background check where permitted. Any background check information will be reviewed in relation to the requirements of the role and applicable law.

Candidates must complete interview activities without the use of artificial intelligence tools or external help unless advance authorization is provided by Inizio Engage or otherwise required by law. This includes using generative AI to create, edit, or guide responses in real time. Candidates may be asked to confirm compliance. Violations may lead to removal from consideration. Requests for reasonable accommodation may be directed to the Talent Acquisition team.

Inizio Engage describes itself as a strategic, commercial, and creative engagement partner focused on healthcare. Its global team combines local expertise with data, science, and technology to create tailored engagement solutions that help clients improve treatment outcomes for patients, payers, healthcare professionals, and providers.

The company’s values include empowering everyone, rising to the challenge, working as one, asking “what if,” and doing the right thing.

The employer notes recognition as a Best Place to Work in BioPharma for 2022, 2023, and 2025, and as a Certified Great Place to Work® for 2021, 2023, 2025, and 2026.

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