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Medical Writer (Medical Information Lead)

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WorkatHome-JobBoard

9d ago

  • Job
    Full-time
    Mid Level
  • Research & Development
    Healthcare
  • Toronto
    Remote

AI generated summary

  • You need an advanced clinical/science degree, 3+ years in medical communication/affairs, strong communication skills, proficiency in Google Workspace and Office 365, and excellent organizational skills.
  • You will create and review medical content, provide scientific accuracy, maintain MI databases, support training, resolve inquiries, and contribute to projects while ensuring compliance and efficiency.

Requirements

  • Advanced Clinical/Science Degree (e.g., MD, PhD, PharmD, or equivalent)
  • Excellent verbal, written and listening communication skills
  • 3 or more years of relevant medical communication experience
  • 3 or more years of direct medical information and/or relevant medical affairs experience in the pharmaceutical industry, a clinical setting or equivalent background and experience
  • Proficient in Google Workspace and Office 365
  • Ability to work both independently and within a group setting
  • Results oriented, excellent organizational skills and ability to work cross-functionally

Responsibilities

  • Create and/or co-create and review medical content for patients, HCPs and payers to ensure scientific rigor, balance and impact, this includes field medical slides (Medical Science Liaisons and Managed Care Liaisons), and standard or complex medical information responses.
  • As needed, provide medical review for scientific accuracy and provide input on the development/use of scientific and promotional materials consistent with approved client processes and policies (Product Review Committee PRC, Reprint Dissemination Committee RDC) and in close partnership with client Medical Content Strategy Leads and MI leadership team to identify and address training needs of Medical Information and Communications staff, internal partners, or external vendors.
  • Write, review, edit and deliver medical content for training purposes, as needed.
  • Author and review US MI responses by identifying and summarizing complex scientific literature in a scientifically accurate, fair balanced, concise and compliant manner to help inform clinical decision-making by HCPs.
  • Plan and maintain a robust product response MI database including launch readiness plans that meets the scientific needs of customers.
  • Serve as subject matter expert for the Therapeutic Area and maintains in-depth product and therapeutic area knowledge.
  • Perform ongoing literature reviews and extracts complex data from scientific literature and arranges the data in an organized format.
  • Provide clinical guidance and medical information to assist the resolution of escalated medical and/or access inquiries from the contact center.
  • Utilize internal scientific narratives and employing creative data visualization techniques to develop medical resources and tools, enhancing scientific engagement through compelling content practices.
  • Review of complex and/or escalated MI cases.
  • Review derivative content and ensuring alignment with MI responses and compliant with relevant review and approval process.
  • Track recurring queries and identify need for creation of new standard responses.
  • Provide relevant stakeholders with actionable insights and recommendations based on knowledge of product/therapeutic area.
  • Create and/or update reference materials and data on file summaries.
  • Contribute to departmental project/task assignments.
  • Participate in cross-functional project teams.
  • Maintain robust understanding of MI contact center processes and technology.
  • Leverage expertise to support the quality and training initiatives for team members in partnership with leadership and or client, as appropriate.
  • Ensure that assigned projects are completed on schedule.
  • Understand how own contribution contributes to results.
  • Understands what the organization delivers and our position within a global context.
  • Builds a network of useful contacts to help get things done more efficiently.
  • Is proactive and anticipatory with solutions to problems in the business.
  • Seeks to stretch own capability, willing to operate outside of comfort zone.

FAQs

Do we support remote work?

Yes, this position is mainly remote.

What qualifications are required for the Medical Writer (Medical Information Lead) position?

An advanced clinical/science degree (e.g., MD, PhD, PharmD, or equivalent) is required.

How many years of experience are necessary for this role?

A minimum of 3 years of relevant medical communication experience and 3 years of direct medical information or relevant medical affairs experience in the pharmaceutical industry or a clinical setting is necessary.

Will I be responsible for creating medical content?

Yes, you will create and/or co-create and review medical content for patients, healthcare professionals (HCPs), and payers.

Is there any training provided for employees?

Yes, there is a library of online training courses available to employees.

What are the leadership responsibilities for this role?

Leadership responsibilities include understanding how your contributions affect results, building a network for efficiency, and proactively finding solutions to business problems.

Are health benefits available immediately upon employment?

Yes, health benefits are available from day one of employment.

Will I need to collaborate with other teams?

Yes, you will participate in cross-functional project teams and work collaboratively with various stakeholders.

How does the company recognize employee contributions?

The company has several recognition programs, including Length of Service Awards, Quarterly Star Awards, and Yearly Inizio Circle of Excellence Awards.

What tools or software should I be proficient in for this job?

You should be proficient in Google Workspace and Office 365.

Is prior experience in the pharmaceutical industry required?

Yes, relevant experience in the pharmaceutical industry or equivalent background is required.

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