Director, EU Medical Affairs (EDG-2025050) at Edgewise Therapeutics
Remote, Scotland, United Kingdom -
Full Time


Start Date

Immediate

Expiry Date

04 Sep, 25

Salary

0.0

Posted On

05 Jun, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Excel, Travel, Powerpoint, External Agencies, Resumes, Communication Skills, Pubmed, Oral Communication, Strategic Thinking, Interpersonal Skills, Databases

Industry

Pharmaceuticals

Description

REQUIRED EDUCATION, EXPERIENCE AND SKILLS:

  • Ability to create and manage the creation of high-quality documents that effectively and clearly convey scientific data, properly identify/target the audience for each document, and communicate clearly and concisely
  • Demonstrated ability to apply strategic thinking and scientific acumen to projects and plans
  • Demonstrated experience interacting with and collaborating with external experts; ability to effectively interact with internal and external stakeholders.
  • Experience managing external agencies and supporting the RFP process to identify agencies and systems.
  • Excellent oral communication and interpersonal skills and written communication skills.
  • Understand clinical trial research, the drug development process, and have experience with reviewing clinical trial data.
  • Prior medical content development or management of medical content experience preferred.
  • Proficiency with computer programs such as MS Word, Excel, and PowerPoint, as well as databases such as PubMed.
  • Travel will vary, plan on 10-20%.
    Edgewise does not accept resumes from recruitment agencies for this position. Please do not send resumes to Edgewise employees or the company location. Edgewise is not responsible for any fees related to unsolicited resumes
Responsibilities

Scientific Communication Content Management & Operations

  • Develop and support conference planning activities, publication planning activities and annual planning and budgeting for Medical Affairs, with an emphasis on EU based activities and support.
  • Provide project and operations support across Medical Affairs workstreams, including organization and development of shared resources, policies and processes.
  • Assess Medical Affairs capabilities, systems, and processes to identify gaps and recommend improvements.
  • Support medical communication materials and publication development as needed.
  • Working with key stakeholders within Medical Affairs, support the planning and execution of Scientific Advisory Boards, ensuring the proper development of content and key strategic questions for the advisor. Also, develop summary slides and communicate the key strategic findings to leadership and other internal stakeholders.
  • In collaboration with key stakeholders within Medical Affairs and other cross-functional partners, support all medical and scientific activities at key medical congresses, including the development of medical and/or therapeutic area booth materials, abstract development, poster development and symposium content development.
  • Develop and track metrics for medical affairs activities
  • Assist in the management of all financial and contractual aspects of assigned projects, including external vendors.
  • Assist in the review of assigned medical content for medical accuracy and fair balance.
  • Develop and expand scientific proficiency in assigned therapeutic area(s).
  • Participate in and lead department initiatives/projects.

IME/Grants/External Sponsored Research (ESRs) Management

  • Serve as the key point of contact for all IME/Grants/ESR-related requests with internal and external stakeholders
  • Partner with cross functional teams to develop and implement an IME/Grants/ESR request process, including proposal review, approval, funding, and execution.
  • Monitor ongoing requests, ensuring milestone tracking, study reporting, and data dissemination.
  • Ensure that requests align with scientific and strategic objectives while maintaining compliance with regulatory and legal requirements.
  • Build and maintain relationships with external medical and scientific communities, including medical societies, KOLs, and academic researchers.
  • Ensure timely and transparent communication with investigators, maintaining strong external partnerships.

EU Clinical Site Liaison

  • Engage and establish relationships with Key Opinion Leaders and other HCPs in the EU in support of all Medical Affairs activities within the region as needed.
  • Work cross-functionally with colleagues within the clinical team in support of clinical trial sites to ensure all medical scientific needs and goals are addressed as needed.
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