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Medical Writing Associate Jobs in Texas (NOW HIRING)

Your Expertise * 0-2 years of professional writing experience (marketing, blogging, social media ... Medical, dental, vision, and life insurance plans with choice and flexibility. * Fertility Support:

Your Expertise * 0-2 years of professional writing experience (marketing, blogging, social media ... Medical, dental, vision, and life insurance plans with choice and flexibility. * Fertility Support:

... writing/development * Experience with complex, large-scale, multi-phase projects preferred ... LEED accreditation or LEED Green Associate preferred. * CSI Construction Documents Technologist ...

Medical Assistant

Katy, TX · On-site

$16.25 - $20.75/hr

Allergy & ENT Associates is looking for a Medical Assistant at our Katy clinic. What are we about ... Excellent verbal and written communication skills COMPUTER SKILLS * Proficient computer skills in ...

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 ...

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Showing results 1-20

Medical Writing Associate information

See Texas salary details

$22.4K

$54.4K

$125.8K

How much do medical writing associate jobs pay per year?

As of Jul 24, 2026, the average yearly pay for medical writing associate in Texas is $54,445.00, according to ZipRecruiter salary data. Most workers in this role earn between $34,000.00 and $64,800.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Medical Writing Associate, and why are they important?

To thrive as a Medical Writing Associate, you need a solid background in life sciences or pharmacy, strong writing skills, and familiarity with medical terminology, often supported by a relevant degree. Proficiency in Microsoft Office, reference management software, and knowledge of regulatory submission systems are commonly required. Attention to detail, organization, and the ability to communicate complex information clearly are standout soft skills for this role. These abilities ensure accuracy, compliance, and effective communication of scientific data in regulatory and clinical documents.

What are some typical challenges faced by Medical Writing Associates when working on regulatory submission documents?

Medical Writing Associates often encounter challenges such as managing tight deadlines, interpreting complex scientific data, and ensuring compliance with strict regulatory guidelines. Collaboration with cross-functional teams—including clinical researchers, statisticians, and regulatory affairs professionals—is essential to clarify data and maintain consistency throughout documents. Attention to detail and the ability to adapt to evolving industry standards are crucial for producing high-quality submissions that meet both regulatory requirements and client expectations.

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

AspectMedical Writing AssociateMedical Writer
Required CredentialsBachelor's degree in life sciences or related field; some roles may require certificationAdvanced degree (Master's or PhD) often preferred; strong writing and scientific background
Work EnvironmentPharmaceutical or biotech companies, CROs, or medical communication agenciesPharmaceutical companies, medical communication firms, or freelance
Employer & Industry UsageEntry to mid-level role supporting medical writing tasksSenior or specialized medical writing tasks, including regulatory documents

The Medical Writing Associate typically supports medical writing projects with a focus on assisting senior writers, while Medical Writers handle more complex, regulatory, or publication writing tasks. Both roles are essential in the medical communication industry, with the associate position often serving as a stepping stone to a full Medical Writer role.

What is a Medical Writing Associate?

A Medical Writing Associate is a professional who creates, edits, and reviews scientific documents related to medicine, healthcare, and clinical research. They are often responsible for preparing regulatory documents, clinical study reports, manuscripts, and other materials that communicate complex medical information clearly and accurately. Medical Writing Associates work closely with researchers, clinicians, and regulatory teams to ensure that documents comply with industry standards and regulatory requirements. This role is essential in the pharmaceutical, biotechnology, and healthcare industries to support drug development and ensure clear communication of scientific data.
What are the most commonly searched types of Medical Writing jobs in Texas? The most popular types of Medical Writing jobs in Texas are:
Infographic showing various Medical Writing Associate job openings in Texas as of July 2026, with employment types broken down into 1% As Needed, 72% Full Time, 25% Part Time, 1% Temporary, and 1% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $54,445 per year, or $26.2 per hour.
Sr. Principal, Medical Science Liaison - Northeast

Sr. Principal, Medical Science Liaison - Northeast

Alcon

Fort Worth, TX • On-site, Remote

Full-time

Medical, Life, Retirement

Posted 4 days ago


Alcon rating

7.5

Company rating: 7.5 out of 10

Based on 67 frontline employees who took The Breakroom Quiz

259th of 535 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.
  • Preferred locations to reside in are NY, PA. MA

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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Compensation and Benefits
Alcon's Total Rewards programs are designed to align incentives with business objectives, support our values, and deliver long-term value. Our compensation approach includes a combination of fixed and variable pay, with short-term and long-term incentive opportunities for eligible roles. Our benefits offerings are designed to support associates and their families across key life events, including programs that promote health and well-being, provide financial security, and support retirement planning.
The salary range posted represents the anticipated hiring range for this role. Actual compensation may vary based on factors such as experience, skills, location, and internal equity, and may fall outside the posted range.
Pay Range
152,150.00 - 196,900.00
Pay Frequency
Annual
Alcon is an Equal Opportunity Employer and participates in E-Verify. Alcon takes pride in maintaining a diverse environment and our policies are not to discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, gender identity, 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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