The Associate Director of Medical Writing will be responsible for leading the development of key regulatory and clinical documents supporting the company's drug development programs, while also ...
The Associate Director of Medical Writing will be responsible for leading the development of key regulatory and clinical documents supporting the company's drug development programs, while also ...
Associate Director, Medical Writing Location: Hybrid 4 days/week in South San Francisco, CA (2 remote flex days per month!) * Relocation Assistance Available About the Opportunity Our client is ...
Associate Director, Medical Writing Location: Hybrid 4 days/week in South San Francisco, CA (2 remote flex days per month!) * Relocation Assistance Available About the Opportunity Our client is ...
Associate Director, Medical Writing (Hybrid - SF Bay Area) We are seeking an experienced Associate Director of Medical Writing to lead the development of high-quality clinical and regulatory ...
Associate Director, Medical Writing (Hybrid - SF Bay Area) We are seeking an experienced Associate Director of Medical Writing to lead the development of high-quality clinical and regulatory ...
Associate Director, Medical Writing (Hybrid - SF Bay Area) We are seeking an experienced Associate Director of Medical Writing to lead the development of high-quality clinical and regulatory ...
Associate Director, Medical Writing (Hybrid - SF Bay Area) We are seeking an experienced Associate Director of Medical Writing to lead the development of high-quality clinical and regulatory ...
Associate Director, Medical Writing
South San Francisco, CA · On-site
$230K - $240K/yr
Calico is seeking an Associate Director, Medical Writing to provide leadership and functional oversight for writing and leading the review/approval process of high quality clinical and regulatory ...
Associate Director, Medical Writing
South San Francisco, CA · On-site
$230K - $240K/yr
Calico is seeking an Associate Director, Medical Writing to provide leadership and functional oversight for writing and leading the review/approval process of high quality clinical and regulatory ...
Associate Director, Medical Writing Location: Hybrid 4 days/week in South San Francisco, CA (2 remote flex days per month!) * Relocation Assistance Available About the Opportunity Our client is ...
Associate Director, Medical Writing Location: Hybrid 4 days/week in South San Francisco, CA (2 remote flex days per month!) * Relocation Assistance Available About the Opportunity Our client is ...
Associate Director, Medical Writing Location: Hybrid 4 days/week in South San Francisco, CA (2 remote flex days per month!) * Relocation Assistance Available About the Opportunity Our client is ...
Associate Director, Medical Writing Location: Hybrid 4 days/week in South San Francisco, CA (2 remote flex days per month!) * Relocation Assistance Available About the Opportunity Our client is ...
Associate Director, Medical Writing Location: Hybrid 4 days/week in South San Francisco, CA (2 remote flex days per month!) * Relocation Assistance Available About the Opportunity Our client is ...
Associate Director, Medical Writing Location: Hybrid 4 days/week in South San Francisco, CA (2 remote flex days per month!) * Relocation Assistance Available About the Opportunity Our client is ...
Associate Director, Medical Writing Location: Hybrid 4 days/week in South San Francisco, CA (2 remote flex days per month!) * Relocation Assistance Available About the Opportunity Our client is ...
Associate Director, Medical Writing Location: Hybrid 4 days/week in South San Francisco, CA (2 remote flex days per month!) * Relocation Assistance Available About the Opportunity Our client is ...
Senior Vice President, Medical Writing and Project Management What you'll do: * Lead authoring strategy and oversee the successful development ofclinical and regulatory documents (e.g., INDs, NDAs ...
Senior Vice President, Medical Writing and Project Management What you'll do: * Lead authoring strategy and oversee the successful development ofclinical and regulatory documents (e.g., INDs, NDAs ...
Medical Writing Operations Manager
Emeryville, CA · On-site +1
$125K - $140K/yr
Position Summary The Medical Writing Operations Manager will drive operational excellence and consistency across Medical Writing deliverables in support of inspection readiness and regulatory ...
Medical Writing Operations Manager
Emeryville, CA · On-site +1
$125K - $140K/yr
Position Summary The Medical Writing Operations Manager will drive operational excellence and consistency across Medical Writing deliverables in support of inspection readiness and regulatory ...
The Grant Writing Program Manager will be responsible for building and leading a team of four or more grant writers, while expanding service offerings to include grant administration and ...
The Grant Writing Program Manager will be responsible for building and leading a team of four or more grant writers, while expanding service offerings to include grant administration and ...
The Grant Writing Program Manager will be responsible for building and leading a team of four or more grant writers, while expanding service offerings to include grant administration and ...
The Grant Writing Program Manager will be responsible for building and leading a team of four or more grant writers, while expanding service offerings to include grant administration and ...
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Oakland, CA · On-site
The Grant Writing Program Manager will be responsible for building and leading a team of four or more grant writers, while expanding service offerings to include grant administration and ...
Quick apply
Grant Writing Program Manager
Oakland, CA · On-site
The Grant Writing Program Manager will be responsible for building and leading a team of four or more grant writers, while expanding service offerings to include grant administration and ...
The Grant Writing Program Manager will be responsible for building and leading a team of four or more grant writers, while expanding service offerings to include grant administration and ...
Quick apply
The Grant Writing Program Manager will be responsible for building and leading a team of four or more grant writers, while expanding service offerings to include grant administration and ...
Visiting Professor of Legal Writing
San Francisco, CA · On-site
$100K - $120K/yr
Visiting Professor of Legal Writing Job Summary: The School of Law at the University of San Francisco is seeking a visiting full-time non-tenure track Legal Research, Writing, and Analysis Professor ...
Visiting Professor of Legal Writing
San Francisco, CA · On-site
$100K - $120K/yr
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Provides writing guidance to internal teams based on organizational goals and company policy, with responsibility for results. * Peer reviews project work and training materials/guidelines drafted by ...
Provides writing guidance to internal teams based on organizational goals and company policy, with responsibility for results. * Peer reviews project work and training materials/guidelines drafted by ...
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Berkeley, CA · On-site
$70K - $199K/yr
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Lecturer Pool - College Writing Programs
Berkeley, CA · On-site
$70K - $199K/yr
Position description The College Writing Programs at the University of California, Berkeley invites applications for a pool of qualified temporary instructors to teach courses in the College Writing ...
Senior content manager that leverages strong writing, user experience, and editorial skills to craft a variety of deliverables. Interfaces with PMs, Engineers, subject matter experts, and technical ...
Senior content manager that leverages strong writing, user experience, and editorial skills to craft a variety of deliverables. Interfaces with PMs, Engineers, subject matter experts, and technical ...
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Sunnyvale, CA · On-site
BA degree in English, Journalism, Technical Writing, a related field or equivalent practical experience. 5 years of experience writing software documentation in a web production environment. Writing ...
Technical Writer
Sunnyvale, CA · On-site
BA degree in English, Journalism, Technical Writing, a related field or equivalent practical experience. 5 years of experience writing software documentation in a web production environment. Writing ...
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| Aspect | Writing | Copywriting |
|---|---|---|
| Primary Focus | Creating various types of content, such as articles, blogs, reports | Creating persuasive content to promote products or services |
| Skills Needed | Research, storytelling, clarity | Persuasion, marketing, concise messaging |
| Work Environment | Media companies, publishing houses, online platforms | Advertising agencies, marketing departments, freelance |
| Common Certifications | Writing courses, journalism degrees | Copywriting certifications, marketing courses |
Writing involves producing a wide range of content for various purposes, focusing on clarity and information. Copywriting specifically aims to craft persuasive messages to drive sales or engagement. While both roles require strong writing skills, copywriters often focus more on marketing strategies, whereas writers may work in journalism, publishing, or content creation.
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Writing professionals, or writers, are content creators who use language to entertain, inform, or persuade audiences. Writers produce all written work available to the public, including books, newspaper articles, blog posts, website content, social media posts, and advertising copy. Examples of conventional writing careers are journalists, novelists, poets, screenwriters, technical writers, and copywriters. Writing professionals may work independently or as a staff writer for a company. Typical job duties include researching, organizing, planning, and outlining written work, in addition to writing, editing, and revising the pieces. To create quality content, writing professionals need excellent language skills, proficiency in computer programs, and a mastery of online tools and resources.
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Other
Medical, Dental, Vision, Retirement, PTO
Posted 15 days ago
Job description
About Us:
Structure Therapeutics develops lifechanging medicines for patients using advanced structurebased and computational drug discovery technology. The company's platform combines the latest advancements in visualization of molecular interactions, computational chemistry, and data integration to design orally available, superior small molecule medicines that overcome current limitations of biologic and peptide drugs. We are advancing a clinicalstage pipeline of differentiated treatments focused on chronic diseases with high unmet need, including cardiovascular, metabolic, and pulmonary conditions.
Structure Therapeutics is led by an experienced group of international drug innovators and financed by top-tier global life sciences investors. The company completed an initial public offering (IPO) in February 2023. With offices in California and Shanghai, Structure Therapeutics has the benefit of being at the center of life science innovation in both the US and China and capitalizing on the strengths of each geographic location.
Position Summary:
The Associate Director of Medical Writing will be responsible for leading the development of key regulatory and clinical documents supporting the company's drug development programs, while also performing quality control (QC) reviews, document formatting, and editing to ensure compliance with regulatory standards, internal guidelines, and best practices. This role requires a seasoned medical writing professional with the ability to manage multiple projects in a fast-paced environment. The ideal candidate will have deep experience in regulatory medical writing and regulatory operations, exceptional attention to detail, and the ability to collaborate effectively with cross-functional teams.
Job Responsibilities:
Regulatory & Clinical Document Development:
- Lead the authoring, review, and finalization of high-quality regulatory and clinical documents, including Clinical Study Protocols, Clinical Study Reports, Investigator Brochures, Briefing Documents, CTD Module 2 summaries, and responses to regulatory agency information requests.
- Ensure all documents comply with applicable regulatory requirements (FDA, EMA, ICH), internal standards, and timelines.
- Provide strategic guidance on regulatory writing best practices, templates, and processes to ensure clarity, consistency, and alignment of messaging across documents.
Quality Control & Document Standards:
- Conduct comprehensive QC reviews to ensure documents are accurate, internally consistent, data-driven, and compliant with regulatory and company standards.
- Ensure documents are properly formatted according to approved templates, style guides, and submission requirements.
- Verify the accuracy and presentation of tables, figures, references, cross-references, and source data.
- Track, analyze, and report quality metrics related to document development and QC activities, identifying trends and driving continuous improvement.
Project & Stakeholder Management:
- Manage medical writing deliverables across multiple projects, ensuring high quality documents with on-time completion.
- Collaborate with cross-functional teams (Clinical Sciences, Clinical Operations, Regulatory Affairs, Biostatistics, Pharmacovigilance, Nonclinical, CMC, and Program Management) to gather and integrate required content.
- Proactively monitor project progress, identify risks, and implement mitigation strategies to support successful outcomes.
Collaboration & Leadership:
- Serve as a key liaison between Medical Writing and cross-functional stakeholders to ensure alignment on content, strategy, and messaging.
- Contribute to cross-functional meetings and strategic planning related to regulatory and clinical documents.
- Provide feedback and support to other medical writers, promoting adherence to standards and continuous enhancement of writing quality.
Education & Qualifications:
- BA, BS or advanced degree (PhD, PharmD, MS, or equivalent) in life sciences, pharmacy, or a related field.
- 5+ years of experience in regulatory medical writing within the pharmaceutical or biotech industry.
- In-depth knowledge of global regulatory requirements, guidelines, and the drug development process.
- Demonstrated experience authoring and contributing to a wide range of regulatory and clinical documents.
- Excellent written and verbal communication skills, with the ability to clearly and effectively convey complex scientific and clinical information.
- Extensive experience conducting quality control (QC) reviews and editing regulatory documents for accuracy, consistency, and compliance.
- Exceptional attention to detail, with a proven ability to identify and correct inconsistencies, errors, and formatting issues.
- Strong project management and organizational skills, including the ability to lead and collaborate with cross-functional teams.
- Proven ability to manage multiple projects simultaneously and thrive in a fast-paced, dynamic environment.
- Experience working with global teams across multiple time zones.
- High proficiency with document management and authoring tools, including Microsoft Word, Adobe Acrobat, EndNote, Veeva, Smartsheet, and related systems.
Structure Therapeutics Inc. is an Equal-Opportunity Employer.
Structure Therapeutics is committed to fair and equitable compensation practices, and we strive to provide employees with total compensation packages that are market competitive. For this role, the anticipated base pay range is $186,000 - $235,000. The exact base pay offered for this role will depend on various factors, including but not limited to the candidate's geography, qualifications, skills, and experience. If you are hired as a remote employee, a requirement is to attend Connection Week one week every month in SSF, CA.
At Structure, base pay is only one part of your total compensation package. The successful candidate will be eligible for an annual performance incentive bonus, new hire equity, and ongoing performance-based equity. Structure Therapeutics also offers various benefits offerings, including, but not limited to, medical, dental, and vision insurance, 401k match, unlimited PTO, and a number of paid holidays including winter shutdown.
Notice to Recruiters/Staffing Agencies
Recruiters and staffing agencies should not contact Structure Therapeutics through this page. All recruitment vendors (search firms, recruitment agencies, and staffing companies) are prohibited from contacting our hiring manager(s), executive team members, or employees.
We require that all recruiters and staffing agencies have a fully executed, formal written agreement on file.
Structure Therapeutics' receipt or acceptance of an unsolicited resume submitted by a vendor organization to this website or employee does not constitute an actual or implied contract between Structure Therapeutics and such organization and will be considered unsolicited and Structure Therapeutics will not be responsible for related fees.
Fraud Alert
To all candidates: your personal information and online safety are a top priority for us. At Structure Therapeutics, direct candidates to apply through our official career page atBambooHR.
Recruiters will always contact you using the domain of Structuretx.com. We will never request payments, ask for financial account information or sensitive information like social security numbers. If you are unsure if a message is from Structure Therapeutics, please email human resources.
About Structure Therapeutics
Sourced by ZipRecruiter
Industry
Biotechnology research and development
Company size
51 - 200 Employees
Headquarters location
South San Francisco, CA, US
Year founded
2017