ZipRecruiter

Log In

1

Associate Medical Writer Jobs in California (NOW HIRING)

previous page

Showing results 41-60

All JobsAssociate Medical Writer JobsAssociate Medical Writer Jobs in California

Associate Medical Writer information

See California salary details

$13

$38

$57

How much do associate medical writer jobs pay per hour?

As of Aug 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 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 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 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 August 2026, with employment types broken down into 1% As Needed, 69% Full Time, 23% Part Time, 2% Temporary, and 5% 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, Clinical Development

Jobtailor

Palo Alto, CA • On-site

$250 - $350/hr

Other

Posted 28 days ago

Job description

Responsibilities
  • Leverage medical expertise and hands‑on clinical experience to promote relevance and rigor of the development program
  • For clinical trials: design, provide medical oversight, and support site and subject retention
  • Serve as a Medical Monitor for clinical trials, ensure study integrity, and track accumulating safety and efficacy data
  • Provide leadership to study teams
  • Ensure successful completion of trial‑related documents (including clinical trial protocols, investigator brochures, medical monitoring plans, site training materials, clinical study reports, health authority responses, standard operating procedures, etc.) with cross-functional team members
  • Anticipate obstacles within a clinical trial, and implement solutions
  • Analyze, evaluate, interpret, and report study results
  • Contribute to drafting and reviewing clinical documents, manuscripts, presentations, and regulatory submissions
  • Contribute to design of the Clinical Development Plan
  • Maintain up‑to‑date knowledge of relevant science, medical information, good clinical practices, and regulatory guidance
  • Collaborate with—and serve as a clinical research resource for—cross‑functional colleagues to optimize product development
  • Cultivate relationships with investigative sites, clinical consultants, and key opinion leaders to represent the interests of the company
  • Contribute to corporate strategic and organizational initiatives
  • Assist with commercial activities as needed
  • Complete assigned tasks thoroughly, accurately, and on time
  • Adhere to rigorous ethical standards
  • Travel up to 20% domestically and internationally for scientific meetings
Requirements
  • M.D. degree
  • Completion of ACGME-accredited residency and fellowship (strongly preferred)
  • Physician licensure in at least one state (strongly preferred)
  • Board‑certified (strongly preferred), with specialty in endocrinology highly desired
  • At least 3 years of industry (other relevant experience e.g. post‑graduate experience in the clinical and/or academic realms may also be considered on a case‑by‑case basis).
  • At least 2 years of experience with clinical trial design and execution
  • Strong track record of scientific and clinical inquiry
  • Possess excellent communication skills (written and oral)
  • Learn quickly, follow complex directions under pressure
  • Multi‑task while remaining organized and attentive to detail
  • Lead both directly and by example
  • Work hard, be a trustworthy and collaborative team player
  • Take initiative and solve complex problems
  • Demonstrate sound judgement in terms of handling complex, confidential, and regulated information
#J-18808-Ljbffr

Apply