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Director Medical Writing Jobs in Texas (NOW HIRING)

We are seeking a Growth and Improvement minded Regional Medical Scientific Director (AKA Medical ... written communicationsAbility to conduct doctoral-level discussions with key external ...

Medical Technician

Baytown, TX

$35K - $44K/yr

Carry out all treatment orders as directed by physician or advanced practice provider (APP) to ... Communicate effectively in writing and verbally in English. d.Work in a fast-paced environment and ...

Medical Technician

San Antonio, TX

$34K - $43K/yr

... all treatment orders as directed by physician or advanced practice provider (APP) to ensure ... Communicate effectively in writing and verbally in English. d.Work in a fast-paced environment and ...

Medical Technician

Baytown, TX · On-site

$22.90/hr

... all treatment orders as directed by physician or advanced practice provider (APP) to ensure ... Communicate effectively in writing and verbally in English. d. Work in a fast-paced environment and ...

... Executive Director, Medical Services and Executive Director. 9. Know, understand, and apply ... Transcribe all written documentation for Certified Nurse Practitioner into applicable electronic ...

... Director, Medical Services and Executive Director. * Know, understand, and apply positive behavior ... Transcribe all written documentation for Certified Nurse Practitioner into applicable electronic ...

... Executive Director, Medical Services and Executive Director. 9. Know, understand, and apply ... Transcribe all written documentation for Certified Nurse Practitioner into applicable electronic ...

We are seeking a dedicated Hospice Medical Director to join our leadership team and provide expert ... Excellent verbal and written communication skills. Personal Traits: * Passion for providing ...

Reporting to the Medical Director, you will provide direction and oversight for patient care ... Excellent verbal and written communication skills. Personal Traits: * Passion for providing ...

... Executive Director, Medical Services and Executive Director. 9. Know, understand, and apply ... Transcribe all written documentation for Certified Nurse Practitioner into applicable electronic ...

... Director, Medical Services and Executive Director. * Know, understand, and apply positive behavior ... Transcribe all written documentation for Certified Nurse Practitioner into applicable electronic ...

Medical Director

Houston, TX · On-site

$238K - $341K/yr

Fluency in English, verbal and written. There may be jobs in some centers that require fluency in ... Completion of Chen Medical training, including Masterful Conversations and meeting facilitation, as ...

Hospice and Palliative Medicine board certification and/or Hospice Medical Director Certification ... Excellent verbal and written communication skills. Personal Traits: * Passion for providing ...

Hospice and Palliative Medicine board certification and/or Hospice Medical Director Certification ... Excellent verbal and written communication skills. Personal Traits: * Passion for providing ...

Hospice and Palliative Medicine board certification and/or Hospice Medical Director Certification ... Excellent verbal and written communication skills. Personal Traits: * Passion for providing ...

Hospice and Palliative Medicine board certification and/or Hospice Medical Director Certification ... Excellent verbal and written communication skills. Personal Traits: * Passion for providing ...

Hospice and Palliative Medicine board certification and/or Hospice Medical Director Certification ... Excellent verbal and written communication skills. Personal Traits: * Passion for providing ...

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Director Medical Writing information

See Texas salary details

$12.1K

$216.5K

$332.6K

How much do director medical writing jobs pay per year?

As of Sep 4, 2026, the average yearly pay for director medical writing in Texas is $216,487.00, according to ZipRecruiter salary data. Most workers in this role earn between $184,500.00 and $265,100.00 per year, depending on experience, location, and employer.

What is a director medical writing?

A Director of Medical Writing oversees the development of clinical and regulatory documents for pharmaceutical, biotech, or healthcare companies. They lead medical writing teams, ensuring high-quality, compliant, and scientifically accurate content for submissions, publications, and regulatory filings. This role involves collaborating with cross-functional teams, managing timelines, and maintaining adherence to industry guidelines. Strong leadership, project management, and writing expertise are essential for success in this position.

What are the responsibilities of a director of medical writing?

A director of medical writing works to write clinical documents, regulatory submission documents, manuals, research grant applications, and other technical medical publications. In this career, your duties include working to manage a team of writers and editors. You may also have author responsibilities yourself. Your employer may expect you to review documents written by other staff members and make or recommend changes. As the director of medical writing, you also create strategies for document writing and implement writing standards plans so that all employees know how to organize their documents to the same standard.

What are the typical daily responsibilities of a director medical writing?

A Director Medical Writing typically oversees a team of medical writers, ensuring the timely creation and quality of clinical and regulatory documents such as study protocols, clinical study reports, and submission dossiers. They collaborate closely with cross-functional teams including clinical operations, regulatory affairs, and biostatistics to align on project goals and timelines. In addition to managing and mentoring staff, they may also review and approve key documents, provide strategic input on document planning, and interact with clients or health authorities. This leadership role often involves balancing multiple projects simultaneously and problem-solving to navigate evolving industry requirements.

What are the key skills and qualifications needed to thrive in the director medical writing position, and why are they important?

To excel as a Director Medical Writing, you need advanced scientific expertise, strong leadership experience, and a background in life sciences or pharmacy, often supported by an advanced degree (PhD, PharmD, or MD). Familiarity with document management systems, regulatory submission platforms (such as eCTD), and certifications like the American Medical Writers Association (AMWA) are highly valued. Superior communication, strategic thinking, project management, and mentoring skills distinguish top performers in this position. These competencies ensure the production of high-quality documents, effective team leadership, and successful navigation of complex regulatory environments.

Do medical writers make good money?

Medical writers, including those in director roles, typically earn competitive salaries that vary by experience, location, and industry sector. Senior positions often offer higher compensation, and proficiency in regulatory guidelines and scientific knowledge can influence earning potential. Overall, medical writing can be a financially rewarding career path for qualified professionals.

Is there a demand for director medical writers?

There is a strong demand for director medical writers due to the growth of the pharmaceutical, biotech, and healthcare industries. These professionals are needed to lead medical writing teams, develop regulatory documents, and ensure compliance with industry standards, often requiring advanced degrees and experience in scientific communication. The role is expected to remain vital as regulatory requirements and the need for clear scientific communication increase.

What does a director of medical writing do?

A director of medical writing oversees the creation and review of scientific and regulatory documents for pharmaceutical, biotech, or healthcare companies. They manage teams of medical writers, ensure compliance with industry standards, and coordinate the development of materials such as clinical study reports, regulatory submissions, and publication content. Strong project management skills and knowledge of regulatory requirements are essential in this role.

What are the most commonly searched types of Medical Writing jobs in Texas?

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

What are popular job titles related to Director Medical Writing jobs in Texas?

For Director Medical Writing jobs in Texas, the most frequently searched job titles are:

What cities in Texas are hiring for Director Medical Writing jobs?

Cities in Texas with the most Director Medical Writing job openings:

Infographic showing various Director Medical Writing job openings in Texas as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 14% Part Time, and 6% Contract. Highlights an 89% Physical, 1% Hybrid, and 10% Remote job distribution, with an average salary of $216,487 per year, or $104.1 per hour.

Regional Medical Scientific Director (aka Medical Science Liaison) Immunology - GI (North Texas)

Merck & Co.

On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 5 days ago


Merck rating

8.0

Company rating: 8.0 out of 10

Based on 51 frontline employees who took The Breakroom Quiz

43rd of 86 rated pharmaceutical


Job description

Job DescriptionWe are seeking a Growth and Improvement minded Regional Medical Scientific Director (AKA Medical Science Liaison, MSL) - in Inflammatory Bowel Disease Immunology that can help drive our Strategic Operating Priorities.-Summary, Focus and PurposeThe Regional Medical Scientific Director (Medical Science Liaison) is a credentialed (i.e., PhD, PharmD, DNP, MD) Director Level Medical Affairs position and therapeutic and disease expert who engages in bidirectional exchange of scientific or medical information with Scientific Leaders (SLs). The role provides balanced, factual, scientific information about non-product areas of interest to the Company and replies to scientific questions from SLs, including questions about Company products. The work is aligned to Scientific Exchange, Research, Scientific Congress Support, and Scientific Insights.You will liaise between the scientific community and the Company to enhance the comprehension of scientific foundations and goals for approved, in-development, and active Company-sponsored trials and/or investigator-sponsored research studies and serve as a role model for other field medical team members in ways that include on-boarding and/or sharing of therapeutic expertise.Consistent adherence to field and corporate policies and Global Medical Scientific Affairs (GMSA) strategy, including field standard operating procedures (SOPs), Good Clinical Practice (GCP) guidelines, and administrative/operational responsibilities.-Responsibilities and Primary Activities- Scientific Exchange Develops professional relationships and engages with national and regional SLs to ensure access to company-approved medical and scientific information on areas of therapeutic interest and Company productsConducts peer-to-peer scientific discussions and maintains a reliable presence with those SLs to ensure they have a medical contact within the companyAddresses scientific questions and directs SL inquiries on issues outside of scope (e.g., grants) to appropriate company resources consistent with applicable policiesMaintains current knowledge and comprehension of dynamic scientific and clinical environment in the Company's Areas of Interest (AOI) for your specific therapeutic area Research Upon Request from Global Center for Scientific Affairs (GCSA)Initiates discussions with SLs and/or potential investigators that include scientific/data exchange within our AOI to determine the alignment with our research strategies, studies concepts, scientific merit, and qualifications for a specific compound or trialEnhances the comprehension of the scientific foundations and goals of investigator-sponsored researchIdentifies barriers to patient enrollment and retention efforts to achieve study milestonesUpon Request from Global Clinical Trial Operations (GCTO)Recommends study sites and identifies potential investigators to participate in phase II-IV clinical development programs, conducts Site Initiation Visits (SIVs), and detects barriers to patient enrollment and retention efforts to achieve study milestonesProtocol lead responsibilities in collaboration with GCTOAddresses questions from investigators and provides information regarding participation in Company-sponsored clinical studies Scientific Congress Support Engages in scientific congresses and medical meetings, facilitates scientific and data exchange for both Company and competitor dataScientific Insights Gathers feedback, data, or information during routine activities that can help the company better comprehend medical or scientific needs, priorities, or concerns of SLs and/or patientsInclusive Mindset and Behavior Work Independently and as a Team member with Integrity - Precision - Accomplishment - Motivational Ambition - Respect - InclusionDemonstrates eagerness to contribute to an environment of belonging, and empowermentLeads by example and serves as a role model for creating, leading, and retaining a workforceMotivation to contribute to an environment of belonging, engagement, and empowermentWorking to transform the environment, culture, and business landscapeLeveraging to ensure business value, per global and inclusion strategyEnsuring accountability to drive an inclusive cultureStrengthening the foundational elements-Required Location:This role covers northern Texas (Dallas).Candidates must reside within the territory.Ability for travel up to 50% within the territoryRequired EducationPhD, PharmD, DNP, DO, or MD-Required Experience - Skills - KnowledgeProven competence and three years of relevant Immunology (Inflammatory Bowel Disease) experience beyond that obtained in the terminal degree programPrincipled verbal and written communicationsAbility to conduct doctoral-level discussions with key external stakeholdersDedication to scientific excellence with a strong focus on scientific education and dialogueExcellent stakeholder management, communication, and networking skillsThorough comprehension of FDA, OIG, HIPAA, and other ethical guidelines, laws, and regulations relevant to the pharmaceutical industry and its customersAbility to organize, prioritize, and work effectively in a constantly changing environmentStrong working knowledge of Microsoft Office Suite (Word, PowerPoint, Excel, Teams, OneNote)Familiarity with virtual meeting platformsPreferred Experience - Skills - Knowledge Additional experience in Immunology Rheumatology and/or DermatologyField-based medical experienceResearch ExperiencedDemonstrated record of scientific/medical publication#eligibleforERPRequired Skills: Clinical Trials, External Collaboration, Gastroenterology, Immunology, Inflammatory Bowel Diseases, Inflammatory Bowel Disease Treatment, Inflammatory Diseases, Medical Affairs, Pharmaceutical Medical Affairs, Professional Networking, Scientific Communications, Strategic ThinkingPreferred Skills: Current Employees apply HERE Current Contingent Workers apply HERE US and Puerto Rico Residents Only:Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process. As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics.--As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities.- For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit:EEOC Know Your Rights EEOC GINA Supplement• We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another's thinking and approach problems collectively.Learn more about your rights, including under California, Colorado and other US State Acts The salary range for this role is $190,800.00 - $300,300.00This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employee's position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs.The successful candidate will be eligible for annual bonus and long-term incentive, if applicable.We offer a comprehensive package of benefits.- Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days. More information about benefits is available at https://jobs.merck.com/us/en/compensation-and-benefits .You can apply for this role through https://jobs.merck.com/us/en (or via the Workday Jobs Hub if you are a current employee). The application deadline for this position is stated on this posting. San Francisco Residents Only: -We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance Los Angeles Residents Only: -We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance Search Firm Representatives Please Read Carefully-Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. -No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.-Employee Status: RegularRelocation:No relocationVISA Sponsorship:No Travel Requirements: 50%Flexible Work Arrangements:RemoteShift:Not IndicatedValid Driving License:YesHazardous Material(s):n/aJob Posting End Date:08/22/2026 *A job posting is effective until 11:59:59PM on the day BEFORE -the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date. Requisition ID:R408880 Salary: . Date posted: 08/21/2026

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