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Pharmd Mph Jobs (NOW HIRING)

Viiv Healthcare

Principal Medical Writer

Durham, NC · On-site

$90 - $120/hr

Advanced degree (e.g., PhD, PharmD, MPH, MS) in life sciences or a related field. * Experience leading regulatory submission projects, including Common Technical Document (CTD) dossiers.

Cosette Pharmaceuticals Inc.

$175K - $230K/yr

MBA, PharmD, MPH, MS Finance, Economics, or related advanced degree preferred. 8+ years of pharmaceutical industry experience. Experience in Market Access, Pricing, Contracting, Finance, Trade ...

Whoop

Senior Clinical Scientist

Boston, MA · On-site

Master's, PhD, MD, PharmD, MPH, or equivalent experience strongly preferred * 6-9 years of experience in clinical research, clinical science, data analysis, epidemiology, medical device, digital ...

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Pharmd Mph information

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$83

How much do pharmd mph jobs pay per hour?

As of Sep 6, 2026, the average hourly pay for pharmd mph in the United States is $52.64, according to ZipRecruiter salary data. Most workers in this role earn between $39.66 and $65.38 per hour, depending on experience, location, and employer.

What is a PharmD MPH?

A PharmD MPH job combines pharmacy (PharmD) and public health (MPH) expertise to improve healthcare outcomes on both individual and population levels. Professionals in these roles work in areas such as healthcare policy, epidemiology, medication safety, and public health advocacy. They may work in government agencies, healthcare organizations, research institutions, or the pharmaceutical industry. The goal is to integrate clinical pharmacy knowledge with public health strategies to enhance disease prevention and health promotion efforts.

What types of projects or initiatives are PharmD MPH professionals typically involved with?

PharmD MPH professionals often work on interdisciplinary projects that blend clinical pharmacy expertise with public health goals, such as medication safety programs, disease prevention initiatives, and community health education. Their daily responsibilities may include analyzing health data, developing policies, implementing public health interventions, or participating in research on medication usage trends. They frequently collaborate with healthcare providers, public health officials, and community organizations to ensure broad impact. This role offers opportunities for career growth into leadership positions in healthcare systems, government agencies, academia, or non-profit organizations focused on health policy and population health.

What are the key skills and qualifications needed to thrive in the PharmD MPH position, and why are they important?

A PharmD MPH professional needs a strong background in pharmacy practice, public health principles, and patient-centered care, supported by doctoral-level pharmacy (PharmD) and Master of Public Health (MPH) degrees. Familiarity with pharmacy management systems, epidemiological software, and public health data platforms, along with appropriate licensure, is typically required. Outstanding communication, problem-solving, and leadership skills are vital for collaborating across clinical, community, and public health environments. These competencies are crucial for effectively improving patient outcomes, advancing public health initiatives, and navigating complex healthcare systems.

What can you do with a Pharmd Mph?

A PharmD MPH graduate can work in various healthcare settings, including clinical pharmacy, public health, healthcare administration, and policy development. They often utilize their knowledge of pharmacology, epidemiology, and health systems to improve patient care and public health outcomes, sometimes requiring licensure or certification depending on the role.
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Pharmd Mph jobs near you
Infographic showing various Pharmd Mph job openings in the United States as of August 2026, with employment types broken down into 2% As Needed, 82% Full Time, 15% Part Time, and 1% Contract. Highlights an 86% Physical, 2% Hybrid, and 12% Remote job distribution, with an average salary of $109,497 per year, or $52.6 per hour.

Principal Medical Writer

Viiv Healthcare

Durham, NC • On-site

$90 - $120/hr

Other

Re-posted 28 days ago

Job description

Principal Medical Writer

ViiV Healthcare, a global specialty HIV company, is seeking a Principal Medical Writer who will lead and deliver high-quality medical writing for complex clinical and regulatory projects. You will work closely with clinical, regulatory, statistical, and cross‑functional teams. This role offers visible impact, professional growth, and meaningful work that aligns with GSK’s mission of uniting science, technology and talent to get ahead of disease together.

We value scientific rigor, clear communication, collaboration, and ownership.

Responsibilities
  • Lead authoring and strategic planning for clinical and regulatory documents, including protocols, clinical study reports, briefing documents, and submission dossiers.
  • Manage end‑to‑end writing projects, coordinating contributors, timelines, and quality checks to meet regulatory and internal standards.
  • Translate complex clinical and statistical data into clear, accurate, and well‑structured scientific narratives for diverse audiences.
  • Act as a subject matter expert on medical writing standards, document structure, and regulatory expectations.
  • Drive process improvement initiatives, support KPI tracking, and contribute to audit readiness and compliance activities.
Basic Qualifications
  • Bachelor’s degree in life sciences, health sciences, or a scientific field.
  • 5+ years of experience in medical or regulatory writing within the pharmaceutical or healthcare industry.
  • 3+ years of experience with regulatory dossier development and Common Technical Document (CTD) module documents.
  • 3+ years of experience independently authoring clinical protocols, clinical study reports, and regulatory submission documents.
Preferred Qualifications
  • Advanced degree (e.g., PhD, PharmD, MPH, MS) in life sciences or a related field.
  • Experience leading regulatory submission projects, including Common Technical Document (CTD) dossiers.
  • Familiarity with statistical concepts and ability to interpret clinical data.
  • Strong problem‑solving skills and ability to adapt to changing priorities.
  • Experience working in multicultural or remote team settings.
  • Proven ability to independently write and manage complex regulatory documents.
  • Strong understanding of International Council for Harmonization (ICH) guidelines and Good Clinical Practice (GCP).
  • Excellent written and verbal communication skills, with attention to detail.
  • Experience managing multiple projects and meeting deadlines in a fast‑paced environment.
Benefits

Learn more about the comprehensive benefits program GSK offers US employees. Please visit GSK US Benefits Summary.

Equal Opportunity Employer

GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, parental status, national origin, age, disability, genetic information, military service or any basis prohibited under federal, state or local law.

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