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Veracyte

Medical Director, Endocrinology

Remote ; RemoteRemote · region unclear
Director+ · 320 Medical Affairs
POSTED 18 OCT
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Pay · posted
$300k–340k
Open for
19d
since 18 Oct
H-1B · FY26
9
certified LCAs
Hiring · 30d
21
0 net · open roles

At Veracyte, we offer exciting career opportunities for those interested in joining a pioneering team that is committed to transforming cancer care for patients across the globe. Working at Veracyte enables our employees to not only make a meaningful impact on the lives of patients, but to also learn and grow within a purpose driven environment. This is what we call the Veracyte way – it’s about how we work together, guided by our values, to give clinicians the insights they need to help patients make life-changing decisions.

Our Values:

  • We Seek A Better Way: We pursue bold ideas, embrace complexity, and keep pushing forward.
  • We Make It Happen: We act with urgency, deliver with excellence, and always find a way.
  • We Are Stronger Together: We engage with empathy, align around what's best for Veracyte, and celebrate as one team.
  • We Care Deeply: We show up with integrity, kindness, and respect for one another.

The Position

The Medical Director is responsible for establishing and implementing the medical affairs strategy for the Afirma/endocrinology franchise to advance the company’s related genomic into clinical practice.

The Medical Director’s responsibilities will align along four focused areas:

(1). Key Opinion Leader (KOL) relationship development;

(2.) Publication strategy and execution that support product adoption and reimbursement;

(3.) Scientific support of the commercial team; and (4.) scientific leadership of R&D and clinical trial strategy and execution.

Responsibilities:

Provide strategic and tactical guidance across the indication/products:

  • Initiate, cultivate and manage relationships with key global opinion leaders to foster a collaborative synergy between Veracyte and academia including but not limited to the following avenues:
  • Medical Advisory Board Meetings
  • Presentations at national and international meetings
  • Peer reviewed publications
  • Investigator initiated research
  • Guideline inclusion
  • Medical policy inclusion
  • Engagement in clinical trials

Provide leadership in the development and execution of Veracyte’s publication plan:

  • Lead the development of Veracyte’s publication plan
  • Collaborate internally and externally to optimize presentations
  • Innovate key message communication to a variety of stakeholders

Participate in Veracyte’s Product Development teams for the development of future products and guidance to all features of tests under development.

  • Provide input during product concept, feasibility, development, validation, and through to product launch.
  • Develop the technology differentiators that help establish product superiority
  • Represent the voice of customer for product design; help to finalize customer requirements so that products will be competitive on market.
  • Plan and design clinical trials including consideration for sample collection during post-launch validation trials, clinical utility trials, and cost effectiveness studies.

Other Responsibilities:

  • Represent Veracyte at the scientific and medical professional organizational meetings.
  • Remain knowledgeable and conversant about new developments and trends in thyroid endocrinology that impact or influence our product portfolio.
  • Provide leadership and contributions to the commercial team in areas including but not limited to:
  • Global marketing and sales
  • Payer relations
  • Medical policy
  • Veracyte team education

Who You Are

  • PhD or MD degree
  • At least 13 years of expertise in scientific and medical writing and presentations which may include:
  • Primary authorship on peer reviewed papers
  • Oral presentations at national or international scientific meetings
  • Responsibility for development and submission of regulatory documents
  • At least 10 years of clinical research experience inclusive of:
  • Research Protocol development
  • Good Clinical Practice Certification
  • Data analytics and basic biostatistics
  • Flexibility to travel up to 30% of the time to meet with key physicians, researchers and payers, and attend/present at industry events domestically and internationally.
  • Excellent communication skills with ability to maintain open communication with people of all backgrounds and expertise inside and outside the Company.
Source · VeracyteFirst seen 2 NovOriginal ↗