ZipRecruiter

Log In

1

Weekend Writing Jobs in Oceanside, CA (NOW HIRING)

Travere

Senior Manager, Medical Writing

San Diego, CA · On-site +1

Department: 107050 Medical Writing Location: San Diego, USA- Remote Be a part of a global team that is inspired to make a difference in the lives of people living with rare disease. At Travere ...

IPS Group

Proposal & Technical Writing Mgr.

San Diego, CA · On-site

$100K - $120K/yr

Develop, write, and edit compelling RFP/RFI responses and proposals in coordination with internal teams. * Own the end-to-end proposal process, including deadline management, formatting, editing, and ...

Tribune Media

Anchor, Weather

San Diego, CA

$115K/yr

Excellent oral, written and interpersonal communication skills * Must have strong organizational ... Must be flexible with schedule and fill-in different shifts, weekends, holidays as needed

Nexstar Media Group

Anchor, Weather

San Diego, CA · On-site

$115K/yr

Excellent oral, written and interpersonal communication skills * Must have strong organizational ... Must be flexible with schedule and fill-in different shifts, weekends, holidays as needed

WOWK-TV

Anchor, Weather

San Diego, CA

$115K/yr

Excellent oral, written and interpersonal communication skills * Must have strong organizational ... Must be flexible with schedule and fill-in different shifts, weekends, holidays as needed

Accelint

Technical Writer

San Diego, CA · On-site

$78K - $98K/yr

Proficiency in writing clear, concise, and user-friendly technical documentation. * Excellent written and verbal communication skills, with keen attention to detail. Preferred Qualifications

Marsh McLennan Agency

Proposal Writer

San Diego, CA · On-site

$56K - $105K/yr

Responsibilities include working closely with the sales team; writing, editing, and maintaining proposal content in a proposal management system; establishing and following a project timeline ...

New

DivIHN

Technical Writer

San Diego, CA · On-site

Experience writing manufacturing documentation. * Will write process instruction, URS, IQ and proper use of equipment, capture process instructions, qualify equipment. * Update them in the quality ...

Accelint Holdings LLC

Technical Writer

San Diego, CA · On-site

$78 - $98/hr

Proficiency in writing clear, concise, and user-friendly technical documentation. * Excellent written and verbal communication skills, with keen attention to detail. Preferred Qualifications

next page

Showing results 1-20

All JobsWriting JobsWeekend Writing JobsWeekend Writing Jobs in Oceanside, CA

Weekend Writing information

See Oceanside, CA salary details

$11

$15

$20

How much do weekend writing jobs pay per hour?

As of Aug 24, 2026, the average hourly pay for weekend writing in Oceanside, CA is $15.70, according to ZipRecruiter salary data. Most workers in this role earn between $12.93 and $18.17 per hour, depending on experience, location, and employer.

What is weekend writing?

Weekend writing jobs are positions or freelance opportunities that specifically require writers to produce content during the weekends. These roles can include writing articles, blog posts, marketing materials, or other forms of written content for clients who need quick turnarounds or have weekend publishing schedules. Such jobs are ideal for individuals looking to earn extra income outside of their regular weekday commitments or for those seeking flexible, part-time work. Weekend writing jobs can be found in various industries, including journalism, digital media, marketing, and content creation.

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

To thrive as a Weekend Writer, you need strong writing and editing skills, a solid grasp of grammar, and often a degree in journalism, communications, or a related field. Familiarity with content management systems (CMS), SEO tools, and digital publishing platforms is typically required. Excellent time management, creativity, and the ability to work independently are standout soft skills for this position. These abilities ensure high-quality, engaging content is produced on tight deadlines, meeting audience and editorial needs over the weekend.

What are some common challenges writers face when working weekend writing shifts, and how can they be managed?

Weekend writing roles often require adapting to tight deadlines and rapid content turnaround, as news and trending topics can emerge unexpectedly. Writers may also have limited access to editors or collaborators outside standard business hours, making self-editing and time management crucial. To succeed, it's helpful to establish a clear workflow, proactively communicate with weekend team members, and utilize available digital collaboration tools. Embracing flexibility and developing strong self-motivation can help writers produce quality work even with less direct supervision.

What are the most commonly searched types of Writing jobs in Oceanside, CA?

The most popular types of Writing jobs in Oceanside, CA are:

What are popular job titles related to Weekend Writing jobs in Oceanside, CA?

For Weekend Writing jobs in Oceanside, CA, the most frequently searched job titles are:

What job categories do people searching Weekend Writing jobs in Oceanside, CA look for?

The top searched job categories for Weekend Writing jobs in Oceanside, CA are:

What cities near Oceanside, CA are hiring for Weekend Writing jobs?

Cities near Oceanside, CA with the most Weekend Writing job openings:

Weekend Writing jobs near you

Manager, Medical Writing Operations

Travere Therapeutics

San Diego, CA • On-site

Full-time

Medical, Life, Retirement, PTO

Re-posted just now

Job description

Department:
107050 Medical Writing
Location:
San Diego, USA- Remote
Be a part of a global team that is inspired to make a difference in the lives of people living with rare disease.
At Travere Therapeutics, we recognize that our exceptional employees are vital to our success. We are a dedicated team focused on meeting the unique needs of rare patients. Our work is rewarding - both professionally and personally - because we are making a difference. We are passionate about what we do.
We are seeking talented individuals who will thrive in our collaborative, diverse, fast-paced environment and share in our mission - to identify, develop and deliver life-changing therapies to people living with rare disease. We stick by our values centered on patients, courage, community, and collaboration to pursue our vision of becoming a leading biopharmaceutical company dedicated to the delivery of innovation and hope to patients in the global rare disease community.
At Travere Therapeutics, we are in rare for life. We continue to courageously forge new paths as we move toward a common goal of elevating science and service for rare patients.
Position Summary:
The Manager, Medical Writing Operations is responsible for leading document specialist support across the Medical Writing function and for authoring and coordinating regulatory, clinical, and safety documents. This position combines medical writing expertise with advanced document production and template management capabilities, serving as a functional subject matter expert resource for writers on complex document formatting, template development, and document quality standards while ensuring deliverables are conformant with in-house style, scientifically accurate, compliant with regulatory requirements, and submission ready.
In addition to supporting the development of regulatory and clinical documents, this position serves as a subject matter expert for document formatting, template development, document quality standards, in-house style guides, and electronic document management systems. The Manager, Medical Writing Operations partners with cross-functional teams to manage and optimize document creation processes, improve efficiencies, and ensure submission-ready deliverables across all phases of product development.
Responsibilities:
  • Serve as a subject matter expert for Microsoft Word, document formatting, style management, templates, and document production best practices.
  • Perform advanced document formatting and publishing activities, including management of complex tables, figures, references, cross-references, automated numbering, table of contents generation, and document quality control.
  • Manage document development timelines, review cycles, and comment resolution activities to ensure high-quality deliverables are completed on schedule.
  • Develop, maintain, and improve standardized document templates, style guides, macros, and formatting tools to support efficient document development and regulatory submissions.
  • Partner with Medical Writing, Regulatory Operations, Clinical Development, Biometrics, Pharmacovigilance, and other functions to ensure documents are submission-ready and comply with regulatory publishing requirements.
  • Author and coordinate the preparation of clinical, regulatory, and safety documents, including protocols, protocol amendments, clinical study reports (CSRs), investigator brochures (IBs), CTD components, and other submission-related documents.
  • Ensure scientific accuracy, consistency, and compliance of documents with company standards and applicable regulatory requirements.
  • Maintain expertise in FDA, EMA, ICH, and other applicable regulatory guidance related to document preparation and submissions.
  • Lead continuous improvement initiatives focused on document quality, process optimization, and operational excellence.
  • Provide guidance and training to document authors and cross-functional teams regarding document standards, templates, formatting requirements, and best practices.
  • Additional duties assigned as needed.

Education/Experience Requirements:
  • Bachelor's degree in Life Sciences, Medical/Health Sciences, Technical Writing, or related field required. Equivalent combination of education and applicable job experience may be considered.
  • Advanced degree (MS, PharmD, PhD) preferred but not required.
  • 6+ years of relevant experience in medical writing, regulatory writing, document management, publishing, or medical writing operations within the biotechnology, pharmaceutical, CRO, or related healthcare industry environment.
  • Experience authoring and/or coordinating clinical and regulatory documents supporting drug development programs and regulatory submissions.
  • Demonstrated expertise in document production, template management, and advanced Microsoft Word functionality.
  • Working knowledge of drug development processes and applicable global regulatory requirements.

Additional Skills/Experience/Requirements:
  • The ideal candidate will embody Travere's core values: Courage, Community Spirit, Patient Focus and Teamwork.
  • Advanced proficiency in Microsoft Word, including styles, templates, section management, automated numbering, cross-references, tables of contents, document comparison tools, and large-document management.
  • Experience with authoring tools and templates (eg, StartingPoint, TransCelerate) and reviewing tools (eg, PerfectIt, Litera) preferred.
  • Experience with Veeva Vault, electronic document management systems, and regulatory document workflows.
  • Experience with publishing tools (eg, Adobe Acrobat, Pragmatic SPL Validator) preferred.
  • Expert scientific writing, editing, and document quality review skills with exceptional attention to detail.
  • Knowledge of FDA, EMA, ICH, and other applicable regulatory requirements governing clinical and regulatory documentation.
  • Strong project management and organizational skills, with the ability to manage multiple priorities and competing deadlines.
  • Excellent interpersonal, verbal, and written communication skills, with the ability to collaborate effectively across multidisciplinary teams.
  • Demonstrated success identifying, leading, and implementing operational improvements that enhance efficiency and document quality.
  • Ability to adapt to changing priorities and evolving project needs within a dynamic development environment.
  • Strong professional experience in a similar role within the biotechnology, pharmaceutical, CRO, or related healthcare industry environment.
  • Well organized with the ability to multitask, prioritize, and manage shifting responsibilities in a dynamic, cross-functional teamwork environment.
  • Ability to adapt to modification and changes to project plans, demonstrating flexibility to implement new strategies and tactics to accommodate these changes.
  • Ability to travel up to 10% domestic and internationally.
  • All positions have an essential job function to be able to perform face to face work with colleagues and/or onsite in San Diego. No role is expected to be 100% remote.

Total Rewards Offerings:
Travere provides comprehensive total rewards offerings that demonstrate our commitment as a diverse, equitable, people-centric, and pay-for-performance organization.
Benefits: Our benefits include premium health, financial, work-life and well-being offerings for eligible employees and dependents, wellness and employee support programs, life insurance, disability, retirement plans with employer match and generous paid time off.
Compensation: Our competitive compensation package includes a combination of both cash compensation (base pay and short-term incentive) and long-term incentive compensation (company stock), designed to recognize, retain, and reward employees.
Target Base Pay Range:
$116,000.00 - $151,000.00
*This information is current as of the date of this posting and may be modified in the future. Actual pay offered to a candidate will depend on a variety of factors including the candidate's experience, education, skills, and location.
Travere will accept applications on an ongoing basis until a candidate is selected for the position.
Travere Therapeutics, Inc. is an EEO/AA/Veteran/Disability Employer.
If you require a reasonable accommodation to complete the application or interview process, please contact us by sending an email to accommodations@travere.com. Please note that this email address is to be used exclusively to request an accommodation with the online application, interview or hiring process only. Travere HR will not reply to emails sent to this address for any other reason.

Apply