Consultant, Medical Monitor (MD), Metabolic Phase III Study

Remote in Anywhere, US • Posted 2 hours ago • Updated 2 hours ago
Contract W2
Remote
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Job Details

Skills

  • Surveillance
  • Documentation
  • Life Insurance
  • Decision Support
  • Forms
  • Data Analysis
  • Medical Classification
  • Collaboration
  • Pharmaceutics
  • Reporting
  • Database
  • Corporate Social Responsibility
  • Accountability
  • Presentations
  • Screening
  • Artificial Intelligence
  • Recruiting
  • Taxes
  • Insurance
  • Law
  • Communication
  • Gmail
  • Routing
  • Management Consulting
  • Life Sciences
  • SAP BASIS
  • Military

Summary

Description:
Remote

Our client is seeking an experienced physician consultant to serve as Medical Lead supporting a critical phase III clinical program in MASH (Metabolic Dysfunction-Associated Steatohepatitis). The role provides dedicated medical oversight of an ongoing clinical study, with responsibility for aggregate data review, safety surveillance, CRO medical monitor support, and regulatory documentation. This is an execution-focused role within the MASH indication. The Medical Lead will function as an extension of the internal physician team with sponsor ownership of the study, ensuring timely safety assessment, protocol interpretation, and regulatory readiness. This role reports to our client's VP of Clinical Development.

Due to client requirements, applicants must be willing and able to work on a w2 basis. For our w2 consultants, we offer a great benefits package that includes Medical, Dental, and Vision benefits, 401k with company matching, and life insurance.

Rate: $180.00 to $205.00/hr. w2

Responsibilities:
  • Provide sponsor oversight and decision support while CRO manages first-line medical monitoring.
  • Respond to protocol interpretation and safety-related queries escalated from CRO medical monitors.
  • Provide documented medical opinions regarding complex safety cases.
  • Review and approve protocol-related clarifications affecting safety oversight.
  • Support updates to informed consent forms and protocol amendments aligned with emerging safety data.
  • Review region-specific protocol modifications for medical appropriateness.
  • Provide medical input and review of safety sections for upcoming regulatory submissions.
  • Ensure consistency of safety narratives and aggregate data analyses across regulatory documents.
  • Support database lock and study close-out, including batch-level subject review of AEs, concomitant medications, and medical history.
  • Perform medical coding review to ensure accuracy and clinical consistency.
  • Review and finalize patient safety narratives for inclusion in Clinical Study Reports.
  • Provide documented sign-off supporting medical readiness for database lock.
  • Collaborate with Clinical Operations, Safety/Pharmacovigilance, and Regulatory teams to ensure alignment on safety interpretation.

Experience Requirements:
  • MD or DO required from the United States or UK.
  • Board certification in a relevant specialty preferred, such as hepatology, gastroenterology, endocrinology, or internal medicine.
  • Demonstrated MASH/NASH, liver, and gastroenterology experience.
  • Prior biotech or pharmaceutical clinical development experience.
  • Experience with medical monitoring and safety review.
  • Experience with aggregate data interpretation.
  • Experience with regulatory safety reporting, including DSUR, PSUR/PSUSAR, and ASR.
  • Experience with database lock review and CSR narrative preparation.
  • Ability to work independently in a high-accountability environment.
  • Strong communication and presentation skills.
  • Nice to have: Experience supporting BLA submission activities.


Recruitment Transparency Notice



Eliassen Group values transparency in our recruitment practices. Please be advised that Eliassen Group utilizes artificial intelligence (AI) tools as part of its initial application screening and hiring process. You may receive email and SMS notifications from the Eliassen Virtual Recruiting Team (, ) inviting you to complete a brief voice screening as part of your application process. These tools assist our hiring teams in different ways, including but not limited to, assistance in reviewing application materials to help identify candidates whose qualifications most closely match the requirements of the position. All AI-assisted evaluations and responses are reviewed by human recruiters before any hiring decisions are made. The use of AI in our process is intended to support fairness, efficiency, and consistency, and Eliassen Group takes measures to prevent bias or discrimination in connection with its hiring practices. By proceeding, you acknowledge, agree, and consent to Eliassen Group's use of these tools, including AI tools, as part of the application and hiring process.

Skills, experience, and other compensable factors will be considered when determining pay rate. The pay range provided in this posting reflects a W2 hourly rate; other employment options may be available that may result in pay outside of the provided range.

W2 employees of Eliassen Group who are regularly scheduled to work 30 or more hours per week are eligible for the following benefits: medical (choice of 3 plans), dental, vision, pre-tax accounts, other voluntary benefits including life and disability insurance, 401(k) with match, and sick time if required by law in the worked-in state/locality.
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About Eliassen Group:

Eliassen Group is a strategic consulting firm that helps organizations reach further and achieve more through our technology, business advisory, and life sciences solutions. For nearly 40 years, we have combined exceptional people, deep domain expertise, and intelligent capabilities to expand our clients' capacity and accelerate meaningful outcomes. We are driven by a purpose to positively impact the lives of our employees, clients, consultants, and the communities we serve.

Eliassen is committed to building a diverse and inclusive team from a variety of backgrounds, perspectives, and skills. We are an Equal Opportunity and Affirmative Action Employer and all employment decisions are based on merit, performance, and business needs. Eliassen does not discriminate on the basis of race, color, gender identity or expression, sexual preference or orientation, sex (including pregnancy, childbirth, and related medical conditions), marital status, creed, religion, physical or mental disability, genetic information, military or veteran status, age, ancestry, national origin, citizenship status, prohibited criminal record inquiries of applicants and employees, or any other category protected by federal, state, or local laws.

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Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.
  • Dice Id: cxelisen
  • Position Id: a1WUQ000001yewT2AQ
  • Posted 2 hours ago

Company Info

About Eliassen Group

Eliassen Group is a leading strategic consulting company that provides business and IT services for our clients as they seek to transform and execute strategies that will drive exceptional outcomes. Leveraging over 30 years of success, we focus on professional services, talent solutions, and life sciences. Eliassen Group offers local community presence and deep networks. We are committed to positively impacting the lives of our employees, clients, consultants, and the communities in which we operate.

Eliassen Group is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, pregnancy, sexual orientation, gender identity, national origin, age, protected veteran status, or disability status.

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