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Md Insurance Medical Reviewer Jobs (NOW HIRING)

ICON

Medical Data Reviewer

Educational scientific background such as MD, PharmD, PhD, Nursing degree, MSc * ≥ 5 years of pharmaceutical clinical/medical data review experience is required, including clinical crosscheck ...

Diedre Moire Corp.

Insurance Underwriter

Darnestown, MD · On-site

$100K - $300K/yr

Insurance Underwriter - Barber Shops & Salons - Germantown, MD Insurance Underwriter Specialty ... medical and dependent care plan, employee assistance program, generous retirement/savings benefits ...

The US Oncology Network

Insurance Reviewer

Eugene, OR · On-site

$22 - $32/hr

Reviews, processes and audits the medical necessity for treatments including radiation oncology ... Obtains insurance authorization and pre-certification for various oncology & hematology related ...

Med Review Inc

Physician Reviewer

Manhattan, NY · On-site

Evaluate medical records, diagnostic findings, and treatment plans using evidence-based guidelines ... MD/DO required with active, unrestricted U.S License * Board Certification required (ABMS or AOA ...

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How much do md insurance medical reviewer jobs pay per hour?

As of Sep 13, 2026, the average hourly pay for md insurance medical reviewer in the United States is $42.06, according to ZipRecruiter salary data. Most workers in this role earn between $22.84 and $54.09 per hour, depending on experience, location, and employer.

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Infographic showing various Md Insurance Medical Reviewer job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 14% Part Time, and 6% Contract. Highlights an 87% Physical, 1% Hybrid, and 12% Remote job distribution, with an average salary of $87,476 per year, or $42.1 per hour.

Sr Manager, Medical Information

Parsippany Troy Hills, NJ • On-site

Scorpion Therapeutics
51 - 200 employees
Learn more about Scorpion Therapeuticsexternal

Other

Medical, Dental, Vision, Life, PTO

Posted 12 days ago

Job description

Senior Manager, Medical InformationJob Overview
  • Respond to unsolicited medical requests for Gilead products from HCPs, the public, and internal colleagues using approved standard documents and up-to-date literature.
  • Use scientific/medical information expertise to drive strategic initiatives and provide globally aligned resources to enable timely decisions and improved patient outcomes.
  • Prepare global resources with local affiliate teams (TA specialist team).
  • Identify, report, and record adverse events and product complaints promptly.
  • Serve as a key medical reviewer in PRC/MRC, providing strategic input, managing complex reviews/escalations, and ensuring scientific rigor and compliant messaging.
  • Contribute to MI strategy and represent MI cross-functionally.
Responsibilities
  • Lead creation of responses to unsolicited medical/scientific inquiries, including complex affiliate/internal requests and escalations.
  • Act as Therapeutic Area (TA) subject matter expert; develop and manage global MI content and response strategies.
  • Author/review/quality-check/approve MI response documents and data-on-file per regulatory/internal requirements.
  • Ensure medical/scientific accuracy; serve as medical reviewer for promotional/medical/Public Affairs materials (PRC/MRC).
  • Execute TA-specific strategies cross-functionally.
  • Maintain/govern MI content repository; update with new data, regulatory changes, and literature surveillance.
  • Analyze MI inquiries for trends/insights/content gaps; translate into actionable recommendations for content strategy.
  • Support TA/department initiatives (product launches, labeling updates, patient engagement).
  • Lead or contribute to global/regional MI projects aligned with strategic MI plans.
  • Support scientific congress presence and inquiries (travel may be required).
  • Oversee external medical writing support and provide line management for non-permanent staff (as applicable).
  • Contribute to MI policies, guidelines, and SOPs.
  • Explore/support AI-enabled tools and digital capabilities to improve MI processes and efficiency.
Basic Qualifications
  • Bachelor’s degree + 8 years’ experience OR Master’s degree + 6 years’ experience OR PhD/PharmD.
Preferred Qualifications
  • Medical Affairs/Medical Information/pharmaceutical industry experience.
  • Strong stakeholder management; written/verbal/interpersonal communication.
  • Ability to analyze/synthesize/communicate complex clinical/scientific data.
  • Knowledge of regulatory/legal requirements for MI/Medical Affairs.
  • Strategic use of MI metrics/customer insights; strong scientific judgment and detail; project management.
  • Knowledge of relevant therapeutic areas/products; leadership in ambiguous situations.
  • Advanced life sciences degree (PhD/PharmD/MD) preferred.
  • MI experience preferred or comparable healthcare/clinical experience required.
  • Experience in medical review of promotional/medical materials preferred.
People Leader Accountabilities
  • Create Inclusion; Develop Talent; Empower Teams.
Benefits (if applicable)
  • Company-sponsored medical, dental, vision, and life insurance; may include discretionary annual bonus/stock-based long-term incentives and paid time off.
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