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Nonclinical Md Jobs (NOW HIRING)

Head of Clinical Affairs

Cambridge, MA · On-site

$150K - $275K/yr

Compile and author summaries of nonclinical data (e.g., toxicology, pharmacokinetics) for inclusion ... PhD in life sciences, PharmD, or MD with a focus on clinical pharmacology or related field. * 8+ ...

... MD Anderson Cancer Center, Baptist Heart Hospital, Baptist Neurological Institute and Wolfson ... Supporting Adult and Pediatric pulmonary care departments in both clinical and non-clinical ...

$70K - $110K/yr

Frederick, MD * Westminster, MD * Mt. Airy, MD * Hagerstown, MD * Manchester, MD Why FOX ... Clinical and non-clinical career growth opportunities Supportive Clinical Community Mileage ...

Showing results 41-60

Nonclinical Md information

See salary details

$11K

$39.6K

$58.5K

How much do nonclinical md jobs pay per year?

As of Sep 12, 2026, the average yearly pay for nonclinical md in the United States is $39,571.00, according to ZipRecruiter salary data. Most workers in this role earn between $28,000.00 and $52,500.00 per year, depending on experience, location, and employer.

What is a nonclinical MD?

Nonclinical MDs are medical doctors who do not practice direct patient care but instead work in roles outside of traditional clinical settings. They may be involved in fields such as medical administration, research, medical writing, pharmaceutical or biotech industries, public health, consulting, or education. These positions utilize the medical knowledge and expertise of physicians in ways that support healthcare systems, develop new treatments, or inform policy, without requiring patient-facing duties. Many doctors pursue nonclinical roles for reasons such as better work-life balance, new career challenges, or interests in broader aspects of healthcare.

What are the key skills and qualifications needed to thrive as a nonclinical MD?

To thrive as a Nonclinical MD, you generally need a medical degree (MD or DO), in-depth clinical knowledge, and experience in areas such as medical affairs, regulatory, or healthcare administration. Familiarity with tools like medical writing software, data analysis platforms, and compliance systems, as well as certifications such as Certified Medical Director (CMD), are often beneficial. Strong communication, analytical thinking, and teamwork skills help Nonclinical MDs effectively collaborate and translate clinical knowledge to business, research, or policy contexts. These skills are essential for ensuring accurate medical input, regulatory compliance, and effective cross-functional collaboration outside direct patient care.

What are some common challenges faced by nonclinical MDs transitioning from direct patient care to nonclinical roles?

Nonclinical MDs often encounter challenges such as adapting to new workflows that do not involve direct patient interaction, learning industry-specific terminology, and building expertise in areas like regulatory affairs, medical writing, or healthcare administration. Many also need to adjust to working within multidisciplinary teams where collaboration with professionals from non-medical backgrounds is essential. However, these roles offer opportunities to leverage clinical knowledge in broader healthcare initiatives and can provide a more predictable work-life balance.

What is the difference between Nonclinical Md vs Clinical Md?

AspectNonclinical MdClinical Md
CredentialsMedical degree, licensing, often research certificationsMedical degree, licensing, clinical practice certifications
Work EnvironmentResearch labs, pharmaceutical companies, regulatory agenciesHospitals, clinics, private practices
Employer & Industry UsagePharmaceutical companies, biotech firms, regulatory bodiesHospitals, clinics, healthcare organizations
Common Search & ComparisonYesYes

Nonclinical Md professionals focus on research, drug development, and regulatory work outside direct patient care, while Clinical Mds are involved in diagnosing and treating patients. Both roles require medical degrees and licensing but differ significantly in work environment and daily responsibilities.

What cities are hiring for Nonclinical Md jobs?

Cities with the most Nonclinical Md job openings:

What states have the most Nonclinical Md jobs?

States with the most job openings for Nonclinical Md jobs include:

What are popular job titles related to Nonclinical Md jobs?

For Nonclinical Md jobs, the most frequently searched job titles are:

Infographic showing various Nonclinical Md job openings in the United States as of August 2026, with employment types broken down into 1% Locum Tenens, 1% As Needed, 79% Full Time, 11% Part Time, and 8% Contract. Highlights an 90% Physical, 2% Hybrid, and 8% Remote job distribution, with an average salary of $39,571 per year, or $19 per hour.

Executive Director, Clinical Pharmacology

Lexington, MA • On-site

Kiniksa Pharmaceuticals
Biotechnology Research and Development • 201 - 500 employees

$315K - $325K/yr

Full-time

Re-posted 3 days ago


Job description

Kiniksa Pharmaceuticals is a commercial-stage biopharmaceutical company developing and commercializing novel therapies for diseases with unmet need, with a focus on cardiovascular indications. With deep expertise in immunology and inflammation, Kiniksa is advancing a growing portfolio of approved and investigational medicines, anchored by its lead product, ARCALYST®, the first and only FDA-approved therapy for recurrent pericarditis. Grounded in rigorous science and bold innovation, the company fosters a highly collaborative, patient-first culture led by accomplished life sciences leaders. At Kiniksa, talented individuals are trusted and empowered to make a real impact-shaping the future of medicine while improving the lives of patients who need it most.
Kiniksa is seeking an experienced Executive Director of Clinical Pharmacology to provide strategic and scientific leadership in the analysis and interpretation of non-clinical and clinical pharmacokinetic (PK), pharmacodynamic (PD), and anti-drug antibody (ADA) data across our portfolio. This role will play a critical part in informing dose selection, clinical trial design, and regulatory strategy for biologic therapies from pre-clinical development through IND and late-stage development.
The successful candidate will work cross-functionally with Nonclinical & Clinical Development, Translational Medicine, Biometrics, Regulatory Affairs, and CMC to ensure rigorous and integrated interpretation of PK and immunogenicity data to support clinical and regulatory decision-making.
This role is based in our Lexington, MA office and requires employees to be onsite five days per week
Key Responsibilities (including, but not limited to):
  • Provide scientific leadership for clinical pharmacology strategy across programs, with emphasis on PK, ADA, and exposure-response relationships.
  • Lead the analysis, interpretation, and integration of PK and ADA data from rodent, non-human primate (NHP), and clinical studies.
  • Guide dose selection and optimization strategies using nonclinical-clinical translation and clinical PK/ADA data.
  • Interpret non-clinical PK and immunogenicity data to support first-in-human starting dose and escalation strategy
  • Serve as the clinical pharmacology subject-matter expert on clinical study teams.
  • Support the design and interpretation of clinical PK/ADA sampling strategies, including timing and assay considerations and assess the impact of immunogenicity (ADA, NAb) on PK, efficacy, and safety across clinical studies.
  • Author and review clinical pharmacology-related sections of regulatory documents such as INDs, BLAs, Clinical study reports (CSRs), and Investigator's brochures

Standout Skills for Impact:
  • Proven track record supporting IND-enabling through late-stage clinical development and experience contributing to or leading regulatory submissions and agency interactions
  • Deep expertise in clinical and non-clinical PK, ADA and immunogenicity risk assessment, exposure-response interpretation
  • Strong understanding of biologic drug disposition, translational PK principles (rodent → NHP → human)
  • Excellent scientific writing and data communication skills
  • Demonstrated ability to influence program strategy through data-driven insights

Qualifications and Experience:
  • PhD in Clinical Pharmacology, Pharmacokinetics, Pharmaceutical Sciences, Pharmacology, or a related discipline (MD or PharmD with relevant experience will also be considered)
  • 12+ years of progressive experience with demonstrated program leadership. Strong hands-on experience with clinical and non-clinical PK data interpretation, Immunogenicity (ADA/NAb) assessment and impact analysis, Biologic drug development, ideally in cardiovascular, rare, and/or inflammatory diseases
  • Strategic thinker with strong scientific judgment
  • Effective cross-functional collaborator and communicator
  • Comfortable operating in a fast-paced, matrixed biotech environment
  • Ability to mentor, develop, and scientifically guide team members
  • High level of accountability, independence, and integrity

Compensation decisions are based on objective criteria including role responsibilities, experience/qualifications, internal equity, geographic location, and external market benchmarks.
Pay Range
$315,000-$325,000 USD
Kiniksa is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, transgender status, age, genetics, national origin, protected veteran status, or disability status, or any other legally protected category. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.
Kiniksa does not accept unsolicited resumes from staffing agencies or search firms. Any resumes submitted without a signed agreement will be considered property of Kiniksa, and no fees will be paid.