Director, Medical Writing - WCH

About This Role

As the Director of Medical Writing- WCH, you are responsible for the writing and / or managing complex marketed and development programs at the portfolio level based on Therapeutic Area, disease state, and / or phase of development. You are also responsible for providing direct supervision for the Medical Writing program leads, including response to potential Medical Writing issues with internal cross-functional teams and external development partners. You will contribute to the long-term growth strategy of the department and ensure that standard procedures are followed across and within projects. You will synchronize prioritization of projects and in some cases, you represents Medical Writing in meetings with governance committees, regulatory agencies, and external development partners. Performs outreach within pharmaceutical / biotech industry to maintain knowledge of evolving / emerging industry standards and to establish medical writing best practices within company.

What You’ll Do

• Have the knowledge and be independently able to prepare clinical and regulatory documents and packages : protocols and amendments, CSRs, IBs, INDs / CTAs, submissions. Thorough understanding of industry best practices to strategically design documents that fulfil their purpose but written with public disclosure requirements in mind.
• Lead the planning, development, and delivery of documents according to ICH guidelines, company SOPs, templates, and regulatory requirements. Support the development and maintenance of SOPs and templates for document development.
• Ability to critically analyze and synthesize complex scientific information, and ensure scientific accuracy and consistency of documents. Develop and integrate messaging and medical writing strategy and ensure consistency through documents in a therapeutic area and / or disease state.
• Collaborate with cross-functional SMEs including (but not limited to), Clinical Development, Regulatory Affairs, Biostatistics, Pharmacovigilance, Clinical Operations.
• Participate in regulatory submission planning, timelines, and document development.
• Manage and / or provide oversight of in-house and / or contractor / vendor medical writers, ensuring high-quality deliverables. Mentor and provide professional development guidance to junior writers. May serve as the MW liaison for one or more Functional Service Providers (FSP).
• Provide mentoring and career development to direct reports to create a high-quality and productive group.
• Review statistical analysis plans and clinical data reports that are incorporated in data-related documents (CSRs, IBs, etc). Provide strategic input to TFL outputs to streamline TFL production.
• Lead departmental initiatives as necessary.

Who You Are

In addition to having exceptional written and communication skills, you successfully worked in a matrix environment where you collaborated with other clinical teams. You have strong regulatory writing experience and strong teamwork capabilities. You have expert knowledge of global requirements related to all aspects of clinical regulatory documentation to support all phases of clinical development (Phase 1-4), and acts as a medical writing subject matter expert to other departments. You have a demonstrated management, scientific, and customer-focused leadership skills.

Required Skills

Additional Information

The base compensation range for this role is : $188,000.00-$259,000.00

Base salary offered is determined through an analytical approach utilizing a combination of factors including, but not limited to, relevant skills & experience, job location, and internal equity.

Regular employees are eligible to receive both short term and long-term incentives, including cash bonus and equity incentive opportunities, designed to reward recent achievements and recognize your future potential based on individual, business unit and company performance.

In addition to compensation, Biogen offers a full and highly competitive range of benefits designed to support our employees’ and their families physical, financial, emotional, and social well-being; including, but not limited to :

Why Biogen?

We are a global team with a commitment to excellence, and a pioneering spirit. As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning, growth, and expanding their skills. Above all, we work together to deliver life-changing medicines, with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives.

At Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired. Read on to learn more about our DE&I efforts.

All qualified applicants will receive consideration for employment without regard to sex, gender identity or expression, sexual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information or any other basis protected by federal, state or local law. Biogen is an E-Verify Employer in the United States.

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