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Associate Medical Writer Jobs in Texas (NOW HIRING)

Pediatric Associates

Medical Receptionist

San Antonio, TX · On-site

$14.75 - $18/hr

Pediatric Associates was founded in Hollywood, FL in 1955. The same clinician-led, evidence-based ... Ability to read, comprehend, follow oral and written instructions. * Knowledge of computer and ...

Lonza

Deviation Investigation Writer - Viral Vector

Houston, TX · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Medical, dental and vision insurance. 401(k) matching plan. Life insurance, as well as short-term ... Minimum of Associate's in Biotechnology, Biology, Chemistry, Engineering, or another scientific ...

New

Gullo Auto

Experienced Express Service Writer

Conroe, TX

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Benefits Benefits include medical, vision and dental insurance, 401K retirement savings plan ... We hire, train, promote and compensate associates on the basis of personal and professional ...

New

Gullo Auto

Experienced Express Service Writer

Conroe, TX · On-site

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Benefits Benefits include medical, vision and dental insurance, 401K retirement savings plan ... We hire, train, promote and compensate associates on the basis of personal and professional ...

New

Gullo Auto

Experienced Express Service Writer

Conroe, TX · On-site

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Benefits Benefits include medical, vision and dental insurance, 401K retirement savings plan ... We hire, train, promote and compensate associates on the basis of personal and professional ...

New

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Showing results 21-40

All JobsAssociate Medical Writer JobsAssociate Medical Writer Jobs in Texas

Associate Medical Writer information

See Texas salary details

$13

$35

$53

How much do associate medical writer jobs pay per hour?

As of Aug 15, 2026, the average hourly pay for associate medical writer in Texas is $36.00, according to ZipRecruiter salary data. Most workers in this role earn between $24.42 and $45.48 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 Texas?

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

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

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

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

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

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

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

Associate Medical Writer jobs near you
Infographic showing various Associate Medical Writer job openings in Texas as of August 2026, with employment types broken down into 75% Full Time, 16% Part Time, 2% Temporary, and 7% Contract. Highlights an 79% In-person, 8% Hybrid, and 13% Remote job distribution, with an average salary of $74,871 per year, or $36 per hour.

Sr. Principal, Medical Science Liaison - Mid Atlantic

Alcon

Fort Worth, TX • On-site, Remote

Full-time

Medical, Life, Retirement

Posted 24 days ago

Alcon rating

7.3

Company rating: 7.3 out of 10

Based on 68 frontline employees who took The Breakroom Quiz

325th of 540 rated manufacturers

Job description

At Alcon, we are driven by the meaningful work we do to help people see brilliantly. We innovate boldly, champion progress, and act with speed as the global leader in eye care. Here, you'll be recognized for your commitment and contributions and see your career like never before. Together, we go above and beyond to make an impact in the lives of our patients and customers.
This role is part of Alcon's Research & Development function, a team that innovates boldly and delivers new products and services to help revolutionize the eye care industry, advance optimal patient outcomes and help people see brilliantly. The Glaucoma Medical Science Liaison (Science/Tech/Engineering Path) is primarily responsible for presenting scientific and clinical information on Alcon products and gathering insights to influence company strategies. You will drive problem-solving and innovation through scientific principles. In this role, a typical day will include:
  • Develop and maintain peer-to-peer relationships with medical experts and key opinion leaders.

  • Support the development and adoption of Alcon products through evidence-based scientific exchange and seek external insights.

  • Provide general medical information in therapeutic areas to practitioners and Alcon associates and respond to unsolicited requests for medical information.

  • Engage in scientific discussions around Alcon product data.

  • Implement medical projects and navigate investigator trials from inception to publication.

  • Maintain thorough knowledge of Alcon products and current medical/scientific research.

  • Work with Med Info and Med Safety to resolve escalated product complaints and medical safety issues, and participate in adverse event reporting and safety responsibilities monitoring.

  • Direct human clinical trials, phases III and IV for company products under development, monitor adherence to protocols, and determine study completion.

  • Provide reporting information for reports submitted to regulatory agencies.

  • Serve as medical consultant to marketing, commercial or research project teams and government regulatory agencies, and act as consultant/liaison with other corporations under licensing agreements.

  • Sign off on product safety reviews.

  • Interface effectively with all other Medical Affairs functions and departments, including Commercial, Quality Assurance, Research and Development, Regulatory Affairs, Market Access, etc.

  • Work with integrity and compliance, observing laws, industry standards, and company policies.

  • All associates must adhere to GxP regulations by strictly following Standard Operating Procedures (SOPs), maintaining accurate and complete documentation, ensuring rigorous quality control, and completing all required training. Associates are responsible for meeting their individual job requirements and contributing to the overall compliance of the organization. Compliance with regulatory requirements and a commitment to continuous improvement are essential to our operations.

WHAT YOU'LL BRING TO ALCON:
  • Bachelor's Degree or Equivalent years of directly related experience (or high school+15 yrs; Assoc.+11 yrs; M.S.+4 yrs; PhD+3 yrs).

  • The ability to fluently read, write, understand and communicate in English.

  • 7 Years of Relevant Experience.

PREFERED EDUCATION AND EXPERIENCE:
  • MD or OD with specialization in Ophthalmology.

  • Advanced knowledge of glaucoma including ophthalmic surgical procedures and optometry.

  • Experience in an ophthalmology or optometry field (academia, industry, clinical practice), including ophthalmic industry or clinical practice.

  • Experience in an ECP-facing role.

  • Working knowledge of the Healthcare System and of the research procedures as well as the ICH guidelines, GCP, and other ethical guidelines.

  • Essential knowledge of clinical trial design, product development, regulatory requirements, payer landscape, and life cycle management.

  • Experience in scientific presentations and basic experience in medical writing and biostatistics.

  • Proven ability and experience developing and fostering peer-to-peer, credible relationships with Medical Experts/decision makers.

HOW YOU CAN THRIVE AT ALCON:
  • Join Alcon's mission to provide outstanding, innovative products and solutions to improve sight, improve lives, and grow your career!

  • Alcon provides robust benefits package including health, life, retirement, flexible time off, and much more!

  • Travel Requirements: 50-60%.

ATTENTION: Current Alcon Employee/Contingent Worker
If you are currently an active employee/contingent worker at Alcon, please click the appropriate link below to apply on the Internal Career site.
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ALCON IS AN EQUAL OPPORTUNITY EMPLOYER AND PARTICIPATES IN E-VERIFY
Alcon takes pride in maintaining an inclusive environment that values different perspectives and our policies are non-discriminatory in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status. Alcon is also committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please send an email to alcon.recruitment@alcon.com and let us know the nature of your request and your contact information.

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