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Writing Associate Jobs in Castro Valley, CA (NOW HIRING)

Enrolled in or have completed an Associates' degree or higher from an accredited institution. * Native-level proficiency in Korean. * Possess a strong writing style with excellent English-language ...

The assignments typically involve in-depth research and writing and creative problem-solving. Where appropriate, summer associates are involved in court appearances, depositions, and firm and client ...

The assignments typically involve in-depth research and writing and creative problem-solving. Where appropriate, summer associates are involved in court appearances, depositions, and firm and client ...

Commercial Litigation Associate - San Francisco/Oakland Posted on April 30, 2026 Responsibilities ... Conducting legal research and writing memoranda * Drafting complex case analyses and preparing ...

Commercial Litigation Associate - San Francisco/Oakland Posted on April 30, 2026 Responsibilities ... Conducting legal research and writing memoranda * Drafting complex case analyses and preparing ...

Associate Attorney

San Francisco, CA · On-site

$125K - $175K/yr

Description: Sher Edling seeks an associate attorney with at least 2 years of litigation or ... Demonstrated analytical and writing skills are required. We are looking for a colleague who will ...

Associate Attorney

San Francisco, CA · On-site +1

$125K - $175K/yr

The associate will work on high-impact environmental litigation representing primarily states ... Demonstrated analytical and writing skills are required. We are looking for a colleague who will ...

Associate Attorney

San Francisco, CA · On-site

$125K - $145K/yr

... writing skills, and the ability to thrive in a fast- paced and dynamic environment. The ideal ... associates, and support staff to ensure cases are handled efficiently Maintain positive client ...

Effective written and verbal communication skills. PHYSICAL DEMANDS AND WORK ENVIRONMENT * Associate required to stand, walk, climb a ladder, and use hands to handle, feel, hold, write, etc. The ...

Effective written and verbal communication skills. PHYSICAL DEMANDS AND WORK ENVIRONMENT * Associate required to stand, walk, climb a ladder, and use hands to handle, feel, hold, write, etc. The ...

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Writing Associate information

See Castro Valley, CA salary details

$53.1K

$124.8K

$199.1K

How much do writing associate jobs pay per year?

As of Aug 11, 2026, the average yearly pay for writing associate in Castro Valley, CA is $124,808.00, according to ZipRecruiter salary data. Most workers in this role earn between $92,300.00 and $150,000.00 per year, depending on experience, location, and employer.

How does a writing associate typically collaborate with other team members during the content development process?

A Writing Associate often works closely with editors, subject matter experts, and designers to ensure content accuracy, clarity, and alignment with project goals. Collaboration may involve participating in brainstorming sessions, revising drafts based on feedback, and adapting writing styles to suit various platforms. Regular communication and feedback loops are essential, as Writing Associates need to balance creative input with organizational guidelines and deadlines. This teamwork not only enhances content quality but also provides opportunities to learn from experienced colleagues.

What are the key skills and qualifications needed to thrive as a writing associate, and why are they important?

To thrive as a Writing Associate, you need strong writing, editing, and research skills, typically supported by a bachelor's degree in English, communications, or a related field. Familiarity with style guides (such as APA or MLA), word processing software, and collaborative platforms like Google Docs is often required. Exceptional communication, critical thinking, and adaptability help you tailor content and feedback to diverse audiences. These competencies are crucial for producing clear, effective writing and supporting the development of others’ written work.

What is the difference between Writing Associate vs Writing Tutor?

AspectWriting AssociateWriting Tutor
CredentialsTypically requires a bachelor's degree, strong writing skillsUsually undergraduate or graduate students with good writing abilities
Work EnvironmentOften works in academic or professional settings, supporting writing projectsPrimarily works in tutoring centers or academic support services
Employer & IndustryUniversities, colleges, or writing centersEducational institutions, tutoring centers

While both roles involve supporting writing, a Writing Associate often collaborates on projects and may have more responsibilities related to content development, whereas a Writing Tutor primarily provides one-on-one assistance to students to improve their writing skills.

What is a writing associate?

Writing Associates are professionals who assist students, faculty, or professionals with writing projects. They provide feedback, guidance, and support to help individuals improve the clarity, structure, and effectiveness of their written work. Writing Associates often work in academic settings, such as writing centers or universities, but can also be found in corporate or nonprofit environments. Their goal is to empower writers to develop their skills and produce high-quality documents.
What are the most commonly searched types of Writing jobs in Castro Valley, CA? The most popular types of Writing jobs in Castro Valley, CA are:
What job categories do people searching Writing Associate jobs in Castro Valley, CA look for? The top searched job categories for Writing Associate jobs in Castro Valley, CA are:
What cities near Castro Valley, CA are hiring for Writing Associate jobs? Cities near Castro Valley, CA with the most Writing Associate job openings:

Associate Director, Medical Writing

Calico

South San Francisco, CA • On-site

$230K - $240K/yr

Full-time

Re-posted 17 days ago


Job description

Who We Are:
Calico (Calico Life Sciences LLC) is an Alphabet-founded research and development company whose mission is to harness advanced technologies and model systems to increase our understanding of the biology that controls human aging. Calico will use that knowledge to devise interventions that enable people to lead longer and healthier lives. Calico's highly innovative technology labs, its commitment to curiosity-driven discovery science and, with academic and industry partners, its vibrant drug-development pipeline, together create an inspiring and exciting place to catalyze and enable medical breakthroughs.
Position Description:
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 documents, in compliance with applicable guidelines and regulations. The successful candidate should be able to effectively collaborate with cross-functional representatives, collaboration partners, external vendors, and stakeholders while maintaining a positive team environment. This role will function as a strong project manager and technical leader with demonstrated scientific and stakeholder-focused leadership skills.
Key Responsibilities:
  • Document Leadership and Authoring:
    • Provides medical writing leadership for clinical programs
    • Acts as a medical writing subject matter expert and collaborates with the Clinical Science team to deliver on clinical documents including clinical study protocols and protocol-related documents (e.g. informed consent forms), clinical study reports, DSURs, Investigator's Brochures, IND clinical summaries/overviews, and CTD components (e.g. Module 2 summaries)
    • Partners with the regulatory function to ensure timely completion of high-quality regulatory documents including health authority meeting requests, briefing packages, responses to requests for information, and other documents as required for submissions
  • Vendor Management: Provides guidance to external writers on prioritization, content and timeline development, and process management to support clinical development and regulatory activities
  • Process Improvement:
    • Develops medical writing best practices (e.g. standard timelines, clinical document templates, Calico Style Guide)
    • Partners with the Quality Assurance team to develop new and update existing Standard Operating Procedures for Medical Writing processes and all clinical documents to ensure compliance with ICH requirements
Position Requirements:
  • Master's degree in a life science discipline from an accredited college or university; PharmD or PhD preferred
  • Minimum of 8+ years of scientific or medical writing experience at a biotech/ pharmaceutical company or clinical research organization setting
  • Expert knowledge of standard clinical regulatory document types and associated regulatory requirements (e.g. ICH guidance, FDA, EMA, Health Canada, Asia-Pacific regulations, etc.)
  • Prior writing experience in Clinical Study Protocols, Clinical Study Reports, DSUR, Investigator's Brochures, IND clinical summaries/overviews, CTD clinical summaries, and partnering with external investigators to support Investigator Initiated Study Trials
  • Expert ability of Microsoft Office Suite, Adobe Acrobat, collaborative review management systems (e.g. SharePoint) and documents management (e.g. Veeva RIM)
  • Experience in resource planning and management experience of contractors
  • Excellent organization skills with a passion for delivering quality results
  • Detail-oriented mindset with excellent verbal and written communication skills
  • Self-motivated and able to work collaboratively
  • Ability to "roll up sleeves" in a start-up environment and a positive can-do attitude
  • Must be willing to work onsite at least 4 days a week

The estimated base salary range for this role is $230,000 - $240,000. Actual pay will be based on a number of factors including experience and qualifications. This position is also eligible for two annual cash bonuses.