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Associate Medical Writer Jobs in Tennessee (NOW HIRING)

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Associate Medical Writer information

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$35

$52

How much do associate medical writer jobs pay per hour?

As of Aug 24, 2026, the average hourly pay for associate medical writer in Tennessee is $35.07, according to ZipRecruiter salary data. Most workers in this role earn between $23.80 and $44.28 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 Tennessee?

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

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

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

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

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

Infographic showing various Associate Medical Writer job openings in Tennessee as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 12% Part Time, and 6% Contract. Highlights an 89% Physical, 1% Hybrid, and 10% Remote job distribution, with an average salary of $72,939 per year, or $35.1 per hour.

Associate Director, Medical Information

Revance

Nashville, TN

$160K - $185K/yr

Full-time

Medical, Life, Retirement, PTO

Posted 20 days ago


Job description

Job Summary:

Reporting to the Vice President of Medical Affairs, the Associate Director, Medical Information will lead the Medical Information function and be responsible for the provision and oversight of high-quality Medical Information services to Revance internal and external customers. This role will manage Medical Information operations, ensure compliant and scientifically accurate responses, maintain standard response materials, monitor inquiry trends, and partner cross-functionally to support Medical Affairs priorities across Revance products.

  • Reporting to: Vice President, Medical Affairs
  • Location:  Nashville, TN - Hybrid (onsite required - relocation support available)
  • Salary Range: $160,000-$185,000 annually + performance bonus 

*The final salary offered will depend upon factors that may include but are not limited to the quality and length of experience, education, and geographic location


Responsibilities/Essential Duties:

  • Lead the Medical Information function, including resource allocation, process improvement, and performance metrics related to inquiry handling, response time, and quality.
  • Generate reports and metrics for Medical Information activities on a regular basis and present to cross-functional teams as requested.
  • Monitor inquiry trends and lead the planning, development, and maintenance of product-related standard response letters and FAQs.
  • Monitor published medical literature and in-house clinical documents; evaluate relevant information and formulate available information into appropriate Medical Information responses.
  • Manage integration between Medical Information and Field Medical Advisor teams, and manage the Medical Information booth at medical congresses to represent Revance Medical Affairs.
  • Monitor the overall Medical Information process and perform quality control; lead business review meetings and identify opportunities for process improvement.
  • Recognize and collect information related to adverse events, product complaints, and medical device reports, and process these reports in accordance with FDA regulations and Revance policies.
  • Create new procedures and update existing procedures, including SOPs and Work Instructions, to ensure alignment of Medical Information practices with established business processes.
  • Handle Medical Information inquiries and document fulfillment within the CRM system.
  • Act as an internal scientific and medical resource; provide training to Sales or other internal functions as needed and actively participate in interdepartmental projects.
  • Provide oversight to Scientific Advisors that serve as Medical Reviewers on the Promotional Review Committee
  • Support the hiring, mentoring, and professional development of Medical Information personnel

Basic Qualifications:

  • PharmD, PhD in biological sciences or equivalent education.
  • Minimum of 6 years of experience in Medical Affairs, including minimum of 3 years of experience in Medical Information services or an equivalent role.
  • Minimum of 2-4 years of management or functional leadership experience.
  • Knowledge of Medical Information/Communication standards within the pharmaceutical industry and applicable regulations.
  • Excellent verbal and written communication skills, including active listening skills.
  • Professional phone etiquette and familiarity with cloud-based phone systems.
  • Experience with Customer Relationship Management (CRM) systems.

Preferred Qualifications:

  • Experience supporting neurotoxins and/or aesthetics products in a Medical Affairs capacity
  • Team oriented with excellent interpersonal and communication skills, both written and oral.
  • Ability to build effective internal relationships.
  • Ability to develop project strategies and execute project details.
  • Highly developed problem-solving capabilities.
  • Ability to effectively learn and convey clinical and non-clinical technical information.
  • Ability to work independently and within team settings.
  • Strong organizational and time-management skills, with the ability to manage multiple projects.
  • Strong computer skills, including Excel, PowerPoint and Word.
  • Ability to travel as needed to support Medical Affairs activities, including medical congresses.


Company Summary:

Revance is a global company developing, producing, and distributing industry-leading, differentiated products across aesthetics, skincare, and therapeutics. Revance drives innovation beyond convention to offer treatment options for individuals across generations. The Company's vision is to redefine excellence in aesthetics, skincare, and therapeutics through science-powered innovation, with an unwavering commitment to its providers, patients, and consumers. Revance's award-winning products are the result of robust research and development, a cornerstone for the Company, driven by renowned scientists. For more information about Revance, please visit us at www.revance.com.

Aesthetics: From the first and only peptide-formulated neuromodulator, DAXXIFY (daxibotulinumtoxinA-lanm) for injection; the first facial fillers designed for dynamic movement, the Teoxane RHA Collection of dermal fillers; and our industry-leading microneedling device SkinPen, among others, our award-winning products are one of a kind. RHA technology is proprietary to and manufactured in Switzerland by Teoxane SA, and Revance is an independent distributor of Teoxane SA to supply the Teoxane RHA Collection of dermal fillers to the U.S. market. SkinPen is owned by Crown Laboratories, Inc., a Revance company.

Therapeutics: Revance is advancing treatments for movement disorders with DAXXIFY (daxibotulinumtoxinA-lanm) for injection, the first and only peptide-formulated botulinum toxin. This differentiated formulation is designed to deliver consistent clinical outcomes and sustained symptom control - addressing a significant unmet need in cervical dystonia.
What Revance invests in you:

  • Competitive Compensation including base salary and annual performance bonus.
  • Flexible PTO, holidays, and parental leave.
  • Generous healthcare benefits, HSA match, 401k match, employer paid life and disability insurance, pet insurance, wellness discounts and much more!


This section of the job description is required by the American with Disability Act (ADA). The ADA requires that job descriptions reflect the physical and mental demands required to effectively perform the essential duties of the job. The ADA prohibits employers from discriminating against a "qualified individual with a disability" in all aspects of the employment relationship. A "qualified individual with a disability" is "an individual who meets the education, experience, skill, and other job-related requirements of a position held or desired, and who, with reasonable accommodation, can perform the essential functions of a specified job."

Revance is an Equal Opportunity employer. All qualified applicants will receive consideration for employment based on merit, without regard to race, color, religion, sex, national origin, disability, protected Veteran Status, or any other characteristic protected by applicable federal, state, or local law.