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Medical Affairs Medical Reviewer - Consultant

  • Consultants
  • Worker Status: Contingent Worker
  • Time Type: Full time
    • US - Remote

Description

General Scope and Summary

SAGE Therapeutics is searching for a creative, resourceful, integrative thinker for a highly visible role that is responsible for ensuring the medical and scientific integrity of external communications. The position will represent Medical Affairs in a cross-functional team and will provide scientific review of medical affairs content and branded/promotional materials. The successful candidate will have an established track record of cultivating partnerships with team members, including individuals within Medical Strategy, Clinical Development, Patient Advocacy, Regulatory, Legal, and Marketing teams. 

Roles and Responsibilities

  • Serve as a member of the internal Medical, Legal, Regulatory review board.

    • Develop strong relationships with key internal stakeholders to provide direction at the initiation, creation, and review of educational and promotional materials.

    • Critically review and approve of promotional and medical materials in compliance with corporate standards and government/industry regulations to ensure medical accuracy, objectivity, and fair-balance.

    • Determine if data/references used are appropriate to support strategy and tactics and provide strong guidance as well as effective negotiation leading to resolution for pieces.

    • Remain current on regulations, best practices, and current trends within the industry and share learnings with others across the review teams.

    • Act as the Medical Reviewer function to ensure best practices are executed to increase the quality and scientific rigor of all Field Commercial and Medical materials.

    • Advise cross-functional teams on how to best communicate the scientific/medical value of products to key internal and external audiences.

    • Demonstrate broad knowledge of disease areas, product labeling, and regulatory guidance.

    • Conduct literature searches in order to ensure the most current and appropriate literature is cited in the materials and to maintain product expertise.

    • Ensure alignment of external medical communication tools with broader disease state and compound communication strategy.

    • May participate in ad hoc projects.

  • Engage with brand medical directors to maintain alignment with Medical Affairs communication strategy for marketed and pipeline compounds.

  • Collaborate with the Preclinical, Clinical Development, and Medical Affairs teams to identify key developments in the understanding of mood disorders and Sage’s pipeline compounds.

  • Liaise with publications and clinical development groups to develop and maintain timely and relevant product expertise.

  • Perform critical analysis and synthesis of internal/external literature related to Sage products and therapeutic areas of focus.

  • Exhibit broad knowledge of assigned therapeutic areas, product labelling, and regulatory guidance.

Experience, Education and Specialized Knowledge and Skills

Must thrive working in a fast-paced, innovative environment while remaining flexible, proactive, resourceful, and efficient. Must have excellent interpersonal skills and the ability to develop important relationships with key stakeholders, including effective conflict management and negotiation skills.

Basic Qualifications

  • MD, DO, or PhD/PharmD required.

  • 5+ years of prior industry experience, preferably in psychiatry/mood disorders.

  • 3-5+ years of combined pharmaceutical industry and/or academic/clinical medicine expertise, including working knowledge of FDA regulations relevant to drug promotion and dissemination for medical and product information.

Preferred Qualifications

  • Previous experience in scientific communications or medical information preferred.

  • Relevant therapeutic background desired (Psychiatry).

  • Ability to analyze and communicate reviewer recommendations and offer alternative approaches to project owners.

  • Experience in Veeva systems.

  • Proficient in MS Office applications.

  • Customer focus: dedicated to meeting the expectations and requirements of internal and external customers.

  • Ability to manage many complex projects in parallel, structuring the actions of many people toward share outcomes.

  • Ability to work independently and as a team player.

  • Be result-oriented with a proven track record of success.

  • Must demonstrate flexibility in response to changing needs and competing demands.

  • Must possess excellent communication skills, relationship building capabilities, and proven ability to influence decision-making without authority.

  • Must be highly perceptive, socially intelligent, and intuitive.

  • Able to perceive non-obvious opportunities by connecting the dots between existing knowledge, new data, and HCP unmet needs in real-time.

  • Must embrace Sage’s core values: Put People First, Improve Lives, Cultivate Curiosity, Do Right, and Forge New Pathways.

Job ID: R001978

#Biotechnology #Careers #ThisIsSage

All Sage new hires will be required to provide documentation that they are fully vaccinated against COVID-19 or, if not, that they are legally entitled to an accommodation due to a medical condition or a sincerely held religious belief.  Requests for accommodation will be considered on a case-by-case basis, and Sage will consider, among other things, whether the proposed accommodation would create an undue hardship.

All qualified applicants will receive consideration for employment without discrimination on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other factors prohibited by law.

EEO IS THE LAW

Equal Opportunity Employer. All qualified applicants will receive consideration for employment without discrimination on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other factors prohibited by law.

EEO is the Law

EEO is the Law - Supplement

Pay Transparency Nondiscrimination

We value our relationships with professional recruitment firms. To protect the interests of all parties, and given the large volume of inquiries received from third-party placement agencies, we are not able to respond to all agency inquiries. We do not accept unsolicited resumes from any source other than directly from candidates for current or future positions. Submission of unsolicited resumes in advance of a signed agreement between our company and a placement agency does not create an implied obligation and, if an unsolicited candidate represented by a placement agency is hired, we are not obligated to pay a fee. Only approved recruitment firms will be allowed to provide services to Sage Therapeutics, Inc.

Employment applications

Employment applications are processed through a website that is not owned or controlled by Sage Therapeutics, Inc. Sage Therapeutics, Inc. makes no representation as to the accuracy of the information contained on websites it does not own or control. Sage Therapeutics, Inc. does not recommend and does not endorse the content of any third-party websites. Your use of third-party websites is at your own risk and subject to the terms and conditions of use for such sites.

#LI-Remote

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