Senior Medical Writer

ICON Clinical Research; México; Híbrido; MXN 600.000 - 900.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Health insurance offering

Retirement planning

Employee Assistance Programme (LifeWor

Life assurance

Childcare vouchers

Descripción de la vacante

ICON Strategic Solutions is seeking a Senior or Principal Medical Writer to lead high-quality regulatory and clinical document development that supports client submissions to regulatory authorities.

You will guide writing strategy, supervise team members, and ensure timelines and formats meet international regulatory standards across therapeutic areas. This role emphasizes independent leadership with minimal supervision and a focus on impactful submissions.

Formación

• Bachelor’s degree in science or health profession required.
• At least 5 years of pharma/biotech writing experience preferred; 3+ years in electronic documents and submissions.
• Experience writing key documents in major international regulatory submissions (e.g., Clinical study reports, IBs, Protocols).

Responsabilidades

• Lead medical writing document preparation and editing.
• Coordinate assignments to writers and review key regulatory documents.
• Lead writing strategy for regulatory submissions and responses.
• Ensure content consistency and regulatory compliance across programs.
• Represent Medical Writing on cross-functional teams and provide guidance.

Conocimientos

Medical writing leadership

Regulatory submissions

Editorial mastery

Communication skills

Educación

Bachelor's degree in science/health profession

Herramientas

Electronic submissions

Descripción del empleo

Principal Medical Writer

At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise.

As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.

We are currently seeking Senior or Principal Medical Writer to join our diverse and dynamic team. At this role you will be responsible for leading the development of high-quality regulatory and clinical documents that effectively communicate scientific and medical information. Your expertise in medical writing will be crucial in supporting our clients’ submissions to regulatory authorities and ensuring compliance with industry standards.

We hire at Medical Writer 2, Senior Medical Writer or Principal Medical Writer level

What You Will Be Doing:

Guides medical writing document preparation, including coordination of assignments to writers, review, and substantive editing of documents. As necessary, may assume primary responsibility for preparation of key regulatory response documents and documents supporting major regulatory submission. Formulates writing approach, develops timelines, and assesses resource requirements for key documents and regulatory submissions within designated therapeutic or functional area. Participates on relevant project teams and task forces, and provides functional and cross-functional guidance on a wide range of issues related to document preparation, including international regulatory guidance and requirements for content and format, work requirements (style, electronic integrity, and process), and project- or therapeutic area-specific guidance related to content and organization of specific documents.

• Leads the writing strategy providing expertise including organization, content, timelines, and resource requirements.

• Provides more complex advanced input for study designs, analysis plans, sections of INDs and marketing applications

• Provides review and substantive editing of contributions, and ensures resolution of issues.

• Within designated therapeutic or compound function, manages deliverables and preparation of documents for submission to regulatory agencies, ensuring consistency of content within therapeutic areas and adherence to regulatory requirements and Sponsor requirements and processes across development programs.

• Represents Medical Writing on cross-functional teams and task forces (related to projects, process, and standards).

• Acts as a key Medical Point of contact for clinical regulatory strategy

• As required, serves as lead writer for important regulatory response documents and key components of regulatory submissions.

• Provides leadership on functional teams that address requirements or issues related to document preparation and production.

• The Principal Medical Writer is seen as an expert in medical writing and performs work independently with minimal supervision.

Your Profile:

• Bachelor’s degree in science, health profession required

• At least 5 years of experience writing for pharma or biotechnology preferred . 3+ years of electronic documents and submissions required.

• Experience with writing key documents included in major international regulatory submissions required like Clinical study reports, IBs, Protocols

• Experience managing writing activities for a major international regulatory submission preferred.

Knowledge and Skills:

• Clear understanding of clinical development, including the phases, processes, and techniques used within a clinical development environment from protocol design through regulatory submission and support for marketed products.

• Understanding of international regulations, ICH guidelines, and applicable international regulatory processes related to document preparation and production (including CTDs).

• Well-developed oral and written communication skills; ability to clearly present technical information within and across functional areas.

• Demonstrated problem-solving and interpersonal skills that facilitate effective interactions within functional and cross-functional teams and with external providers

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What ICON can offer you:

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our benefits examples include:

• Various annual leave entitlements

• A range of health insurance offerings to suit you and your family’s needs.

• Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.

• Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being.

• Life assurance

• Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.

Visit our careers site (https://careers.iconplc.com/benefits) to read more about the benefits ICON offers.

At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here (https://careers.iconplc.com/reasonable-accommodations)

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

Are you a current ICON Employee? Please click here (https://wd3.myworkday.com/icon/d/task/1422$1235.htmld) to apply