Associate Director, Medical Writing

Position Title: Associate Director, Medical Writing

Reports to: Senior Director, Regulatory Affairs

Status: Regular, Full-time, Exempt

Summary: We are seeking a highly motivated Associate Director, Medical Writing, to be responsible for the planning, coordination, and oversight of all medical writing activities within the company. In this role, you will lead the Medical Writing function and be responsible for developing and implementing a standardized process for the development of clinical and regulatory documents and managing external resources. Success in this role requires you to be adept at working cross-functionally with stakeholders.

This position is based in our South San Francisco, CA, location, with flexibility to work remote some of the time, and will be required to be on-site for meetings on a routine basis.

Specific responsibilities include, but are not limited to:

• Planning, managing, and aligning medical writing activities and communication across multiple projects and development programs

• Overseeing the development of critical documents, including Investigator Brochures, protocols/protocol amendments, and clinical study reports, in compliance with SOPs, ICH E3 guidelines, other applicable regulatory guidance documents, and local requirements

• Supporting the selection of CROs and vendors and providing project-level oversight of CROs and other vendors

• Developing the medical writing functional area, including creation of standardized policies, procedures, work instructions, timelines, document tools and templates, style guide, and best practices

• Engaging and communicating with functional area leads and stakeholders across development programs to support medical writing activities

• Providing leadership in planning and contributing to key regulatory submissions to US and global health authorities (NDAs, MAAs, INDs, annual reports, DSURs).

• Ensuring key messages are clear and consistent within and across documents

• Contributing strategically and scientifically at the project and/or study team level

• Forecasting costs for individual medical writing projects

• Generating and tracking medical writing project budgets against planned budget and timelines

• Partnering with legal and financial functions to negotiate medical writing contracts and budgets

• Identifying and anticipating issues related to budget and project milestones and lead mitigation and resolution efforts for issues identified

• Creating and regularly updating medical writing project timelines and ensure that medical writing timelines are in sync with the program timelines

• Acting as a key contributor to the organization cross-functionally to promote organizational goals and knowledge sharing

• Leading and driving process improvement initiatives for medical writing

• Setting up and leading kick off meetings and comment resolution meetings

Qualifications include:

• Bachelor's degree with 8+ years of pharmaceutical/biotechnology medical writing experience including development of regulatory documents for Phase I-III clinical trials. A Master's or PhD degree may be considered in place of years of relevant experience.

• Subject matter expert in the regulatory medical writing process with strong attention to detail

• Demonstrated ability to communicate and write clearly, concisely, and effectively. Aptitude for compilation, analysis, and presentation of data

• Expert knowledge of AMA style, medical terminology, and clinical data analysis

• Demonstrated experience in the preparation of protocols, study reports, investigator brochures, safety updates, and other clinical and regulatory documents required for IND and MAA submissions

• Demonstrated experience in a lead medical writing role managing projects of varying size and complexity, preferably within a pharmaceutical company or contract research organization (CRO)

• Experience managing medical writing vendors and/or contract medical writers

• Excellent communication skills to ensure that medical writing plans and processes are transparent, strict timelines are met, and risks, issues, and results are clear to all stakeholders

• Outstanding organizational skills with the ability to multi-task, prioritize, negotiate, manage competing priorities, analyze and solve problems

• Thorough knowledge of regulatory and compliance requirements for medical writing, including ICH E3 and other applicable guidelines

• Willing to embrace change and work in a changing environment

• Able to work collaboratively across cultures and geographies

• Proficient in Microsoft Word, Project, PowerPoint, Excel

• Proficient in Adobe Acrobat, and electronic document templates (e.g. eCTD templates)

Pay Range:

$144,000 - $160,000/yr

The stated pay range for this position reflects the San Francisco Bay Area job market. Assembly Bio establishes pay ranges based on geographic work locations. Additional factors such as academic credentials and relevant experience will influence the actual salary offered.

About Assembly Bio

Assembly Bio (NASDAQ: ASMB) is an ambitious biopharmaceutical company with cutting-edge therapeutic clinical candidates capable of improving the lives of millions living with chronic hepatitis B virus (HBV) infection around the world, and research and preclinical programs focused on the discovery of novel antivirals to treat devastating viral diseases, including HBV, hepatitis delta virus (HDV) and herpesviruses.

We pride ourselves on creating a culture and work environment that is scientifically driven, ambitious, and collaborative. We encourage diversity of thought that leads to great innovation and are looking to add great people to our dynamic team who are driven to transform the lives of patients. We set our sights high-and pursue our goals with determination. Our unique organization stands ready to welcome talented, motivated individuals, who share our ambitions.

As an equal opportunity employer, we are committed to diversity and inclusion and will not tolerate discrimination and harassment of any kind. All employment decisions are based on business needs, job requirements and individual qualifications, without regard to race, color, religion or belief, national, social or ethnic origin, sex (including pregnancy), age, physical, mental or sensory disability, HIV status, sexual orientation, gender identity and/or expression, marital, civil union or domestic partnership status, past or present military service, family medical history or genetic information, family or parental status, or any other status protected by the laws or regulations in the locations where we operate.

Information for Recruitment Agencies

Assembly Bio does not accept from recruiters/agencies any unsolicited resumes, or any candidate information including blinded resumes and will not be responsible for any fees related to resumes or candidate information that is unsolicited. Please do not contact hiring managers or Assembly Bio employees directly with any information related to a resume or a candidate. We handle all recruiting through our internal Human Resources team, and we will reach out to you directly should we wish to engage in a search.