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Associate Medical Writer Jobs in California (NOW HIRING)

Axis Community Health

The Associate Medical Director (AMD) plays a key leadership role in ensuring high-quality, patient ... Excellent writing, business communication, editing, and proofreading skills. * Ability to interact ...

Kids for the Future

$307K - $363K/yr

... the Associate Medical Director of Psychiatry & Addiction Medicine (AMD) provides clinical ... written policy and procedures of El Dorado County Community Health Center, written in accordance ...

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Associate Medical Writer information

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$57

How much do associate medical writer jobs pay per hour?

As of Sep 12, 2026, the average hourly pay for associate medical writer in California is $38.13, according to ZipRecruiter salary data. Most workers in this role earn between $25.87 and $48.17 per hour, depending on experience, location, and employer.

What does an associate medical writer do?

An Associate Medical Writer is responsible for creating scientific documents, such as clinical study reports, regulatory submissions, and manuscripts for publication. They work closely with medical professionals, researchers, and regulatory teams to ensure accuracy and compliance with guidelines. Their role often involves interpreting complex scientific data and presenting it in a clear, concise manner for different audiences. Associate Medical Writers are typically early in their medical writing careers and receive guidance from more senior writers as they develop their skills.

What are the key skills and qualifications needed to thrive as an associate medical writer?

To thrive as an Associate Medical Writer, you need a solid background in life sciences, strong writing abilities, and attention to detail, often supported by a relevant degree such as biology, pharmacy, or medicine. Familiarity with referencing tools (e.g., EndNote), medical literature databases (e.g., PubMed), and proficiency in Microsoft Office are typically required. Excellent communication, time management, and the ability to interpret complex scientific data set standout candidates apart. These skills ensure that scientific information is accurately and clearly communicated to varied audiences, supporting effective healthcare and regulatory decision-making.

What are some common challenges faced by associate medical writers during their first year on the job?

In their first year, Associate Medical Writers often find it challenging to quickly adapt to diverse writing styles and strict formatting guidelines required by different clients or regulatory bodies. Balancing tight deadlines while ensuring scientific accuracy and compliance can also be demanding, especially when juggling multiple projects. Additionally, learning to effectively collaborate with multidisciplinary teams—including clinicians, researchers, and senior writers—requires strong communication and organizational skills. However, with mentorship and constructive feedback, these challenges become valuable learning opportunities for professional growth.

What is the difference between Associate Medical Writer vs Medical Writer?

AspectAssociate Medical WriterMedical Writer
Required credentialsBachelor's degree, often in life sciences or related fieldBachelor's or higher degree, often with some experience
Work environmentEntry-level, training-focused, often in pharmaceutical or biotech companiesMore independent, involved in complex document creation for regulatory or scientific purposes
Employer usagePharmaceutical, biotech, medical communications agenciesPharmaceutical companies, CROs, medical communication firms

The main difference between an Associate Medical Writer and a Medical Writer lies in experience and responsibility. Associate Medical Writers are typically entry-level, focusing on learning and supporting document preparation, while Medical Writers handle more complex projects independently. Both roles require similar educational backgrounds and are common in the pharmaceutical and biotech industries.

What are the most commonly searched types of Medical Writer jobs in California?

The most popular types of Medical Writer jobs in California are:

What are popular job titles related to Associate Medical Writer jobs in California?

For Associate Medical Writer jobs in California, the most frequently searched job titles are:

What job categories do people searching Associate Medical Writer jobs in California look for?

The top searched job categories for Associate Medical Writer jobs in California are:

What cities in California are hiring for Associate Medical Writer jobs?

Cities in California with the most Associate Medical Writer job openings:

Associate Medical Writer jobs near you
Infographic showing various Associate Medical Writer job openings in California as of September 2026, with employment types broken down into 1% As Needed, 77% Full Time, 16% Part Time, and 6% Contract. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution, with an average salary of $79,311 per year, or $38.1 per hour.

Associate Medical Director, Oncology

Redwood City, CA • On-site

Corcept Therapeutics
Biotechnology Research and Development • 51 - 200 employees
Learn more about Corcept Therapeuticsexternal

$229K - $269K/yr

Full-time

Re-posted 3 days ago

Key responsibilities

  • Support the ongoing and planned execution of Oncology clinical trials.

  • Provide scientific oversight and medical expertise for clinical studies, including design, development, and implementation from Phase I through Phase III.

  • Participate in regulatory activities, safety monitoring, and analysis of clinical data related to Oncology programs.

Job description

For more than 25 years, Corcept has been singularly focused on the science of cortisol, a powerful hormone that when unregulated, can play a role in a broad range of diseases.
Our commercial portfolio includes treatments for hypercortisolism and oncology, and the company has discovered more than 1,000 proprietary selective cortisol modulators and glucocorticoid receptor antagonists. With advanced clinical trials in patients with hypercortisolism, solid tumors, ALS and liver disease, Corcept is unlocking the power of cortisol modulation to help address some of the most devastating diseases patients face today.
Corcept is headquartered in Redwood City, California. To learn more, visit www.corcept.com.
As an Associate Medical Director, you will support the ongoing and planned execution of the Oncology trials and contribute to clinical development planning for Oncology.
Responsibilities:
  • Act as a clinical scientist and clinical subject matter expert for both Company team members and for external contacts related to the assigned therapeutic programs
  • Provide training and ongoing input to all members of the clinical team on medical and scientific issues related to the therapeutic field in question
  • Provide scientific oversight for Company operational staff, CROs, and clinical trial sites in all areas related to the therapeutic programs
  • Design, develop and, implement clinical studies for the applicable drug candidate, from Phase I through Phase III
  • Develop and participate in the writing and review of protocols, investigator brochures, study reports and other clinical and regulatory documents
  • Establish and approve scientific methods for design and implementation of applicable clinical protocols, data collection systems and final reports
  • Acts to provide medical oversight and safety monitoring for ongoing clinical trials including participation in SAE reporting and serving on the safety committee
  • Play a key role in the analysis, interpretation and delivery of high quality clinical data
  • Interact with principal investigators and opinion leaders to facilitate clinical trials research
  • Participate in appropriate regulatory discussion and activities, including the filing of IND's, CTXs, NDA/MAAs, throughout the development cycle
  • Participate in clinical study report conceptualization, development and writing for global regulatory submissions
  • Work closely and collaboratively with other functions, e.g. clinical operations, safety, biometrics, regulatory, medical writing, medical affairs and commercial
  • Develop and give internal and external presentations as subject matter expert for the therapeutic area
  • Participate in the development and review of publications
  • Prepare and monitor clinical trial budgets in collaboration with clinical operations and R&D finance
  • Participate in the management of human resources in a matrixed environment - recruitment, performance management, succession planning, talent management, etc.
  • Serve as liaison to the commercial team on medical issues

Preferred Skills, Qualifications and Technical Proficiencies:
  • Demonstrate strong clinical and scientific knowledge
  • Excellent communication skills with proven leadership experience and the ability to interact in a cross functional environment
  • Comfortable in a fast-paced, small company environment and able to adjust workload based upon changing priorities

Preferred Education and Experience:
  • MD, board-certified (or eligible), preferably in Oncology
  • 2+ years' clinical development experience in the biotechnology/pharmaceutical industry or an academic clinical trial unit
  • A proven track record of scholarly clinical research demonstrated by publications in top-tier journals

The pay range that the Company reasonably expects to pay for this headquarters-based position is $229,300-$269,800; the pay ultimately offered may vary based on legitimate considerations, including geographic location, job-related knowledge, skills, experience, and education.
Applicants must be currently authorized to work in the United States on a full-time basis.
For information on how Corcept collects, uses, discloses, protects, and otherwise processes personal information and an explanation of the rights and choices available to you with respect to your personal information, please refer to our Privacy Notice link.
Corcept appreciates the commitment and hard work of all our team members as we strive to discover and develop novel treatments for patients with serious unmet medical needs.
Please visit our website at: https://www.corcept.com/
Corcept is an Equal Opportunity Employer
Corcept will not conduct interviews via text message or messaging platforms and will not ask you to download anything as part of your interview. Though we use third-party tools to help with advertising our jobs, please be vigilant in checking that the communication is in fact coming from Corcept.

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