• Job Description

  Req#: 35126-JOB
  What if the work you did every day could impact the lives of people you know? Or all of humanity?
  At Illumina, we are expanding access to genomic technology to realize health equity for billions of people around the world. Our efforts enable life-changing discoveries that are transforming human health through the early detection and diagnosis of diseases and new treatment options for patients.
  Working at Illumina means being part of something bigger than yourself. Every person, in every role, has the opportunity to make a difference. Surrounded by extraordinary people, inspiring leaders, and world changing projects, you will do more and become more than you ever thought possible.
  Illumina, Inc. is seeking an exceptional scientific leader in Oncology with a strong background in cancer diagnostics, clinical evidence generation study and data management and a demonstrated strong commitment to patient-centered precision genomics. This role will focus on driving Illumina's objectives on integrating the adoption of sequencing technologies and comprehensive genomic insights into clinical practice guidelines, precision medicine treatment pathways, reimbursement strategies and patient care management in oncology.
  Key Responsibilities:
  • Provides study management and assures successful conduct of clinical studies consistent with applicable regulations, guidelines, and procedures.
  • Oversees and manages clinical project personnel and/or consultants.
  • Conducts clinical compliance activities; Manages clinical study budgets.
  • Reviews, assesses, and interprets data from ongoing and completed studies.
  • Writes abstracts, papers, and manuscripts related to study results as required. Monitors compliance with all company standard operating procedures (SOPs), GCP, FDA and applicable international regulations concerning clinical activities.
  • Provide subject matter expertise in comprehensive genomic profiling, whole genome and transcriptome sequencing, plasma-based testing, and other topics in interactions with internal and external stakeholders.
  • Lead the development of scientific education content and in-house training for the Medical Affairs team and other appropriate staff as required, and support adaptation of training content for clinical specialists in collaboration with Marketing and other relevant internal stakeholders
  • In collaboration with Scientific Affairs, lead the development and implementation of scientific publication plans including Oncology congress planning
  • Participate in local, regional, and international meetings, congress, and symposia, contributing to supporting Illumina’s objectives and prepare conference summaries.
  Responsibilities include but are not limited to those listed above and changes to individual responsibilities may occur due to business needs.
  Qualifications Minimum Requirements
  Experience/Education:
  • Typically requires a minimum of 8 years and a Master’s degree; or a PhD with 5 years experience in pharmaceutical and/or diagnostic medical affairs planning and management experience.
  • Experience in managing clinical studies in oncology diagnostics will be valuable.
  • Broad knowledge of all areas within a Corporate sub-function or a function within an operation. Has depth of technical knowledge in function derived from experience in individual contributor and middle management roles.
  • Requires high level understanding of oncology and genetics markets and sales opportunities for the company’s products.
  #LI-REMOTE
  The estimated base salary range for the Senior Manager, Medical Affairs - Oncology Studies (Remote) role based in the United States of America is: $149,600 - $224,400. Should the level or location of the role change during the hiring process, the applicable base pay range may be updated accordingly. Compensation decisions are dependent on several factors including, but not limited to, an individual’s qualifications, location where the role is to be performed, internal equity, and alignment with market data. Additionally, all employees are eligible for one of our variable cash programs (bonus or commission) and eligible roles may receive equity as part of the compensation package. We offer a wide range of benefits as innovative as our work, including access to genomics sequencing, family planning, health/dental/vision, retirement benefits, and paid time off.
  
  
  At Illumina, we strive to foster a diverse and inclusive workplace by cultivating an environment in which everyone contributes to our mission. Built on a strong foundation, Illumina has always been rooted in openness, collaboration, and seeking alternative views and perspectives to propel innovation in genomics. We are proud to confirm a zero-net gap in pay, regardless of gender, ethnicity, or race. We also have several Employee Resource Groups (ERG) that deliver career development experiences, increase cultural awareness, and demonstrate our collective commitment to diversity and inclusion in the communities we live and work. We are proud to be an equal opportunity employer committed to providing employment opportunity regardless of sex, race, creed, color, gender, religion, marital status, domestic partner status, age, national origin or ancestry, physical or mental disability, medical condition, sexual orientation, pregnancy, military or veteran status, citizenship status, and genetic information. If you require accommodation to complete the application or interview process, please contact accommodations@illumina.com. To learn more, visit: https://www.dol.gov/ofccp/regs/compliance/posters/pdf/eeopost.pdf

• About the company

  Illumina and GRAIL have entered into a definitive agreement under which Illumina will acquire GRAIL for cash and stock consideration of $8 billion.

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