United States flag

Research Scientist, Multiple Myeloma - Translational Medicine

United States - California - Santa Monica, United States - California - Foster CityResearchRegular

Job Description

For Current Kite Pharma Employees and Contractors:

Please log onto your Internal Career Site to apply for this job.

We’re here for one reason and one reason only – to cure cancer. Every moment is dedicated to developing treatments and every action moves us one step closer to our goal. We’ve made incredible scientific breakthroughs and our pioneering personalized CAR T-cell therapies have changed the paradigm. But we're not finished yet.

Join Kite, as we make even bigger advances in cancer therapies, and help shape where our business and medical science goes next.

We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Kite and help create more tomorrows.


Job Description

The Research Scientist will design and execute biomarker and translational strategy for the clinical development of Kite’s chimeric antigen receptor (CAR-T) programs in Multiple Myeloma. As a member of the Translational Medicine Clinical Pharmacology team, you will be at the intersection of Research and Clinical Development, providing valuable insight into the function of CAR-T cells in patients and the development of potential prognostic tools. You will facilitate clinical trial execution, synthesize scientific data, communicate key findings cross-functionally.

Job Responsibilities

  • Directs and establishes pharmacokinetic and pharmacodynamic (PK/PD) analysis to support clinical pharmacology for CAR T clinical trials in Multiple Myeloma
  • Serves as Biomarker lead on clinical study teams to oversee delivery of pharmacology data and documentation required for pivotal and registrational study filings
  • Reviews and contributes to clinical protocol design and study activities
  • Identifies and establishes agreements with contract research organizations (CRO) and support the transfer of novel methods
  • Collaborates with Clinical development teams including Clinical Operations, Regulatory, Clinical Data Management and Biometrics/Stats to advance data acquisition and analyses of clinical trial data
  • Guides the resolution of clinical pharmacology/translational queries from regulatory agencies, supports writing and reviewing responses to regulatory queries.
  • Supports the preparation of data packages for publication with medical writers, presentation and/or submission to regulatory agencies
  • Collaborates with Bioinformatics and Statistical teams for exploratory biomarker correlative studies and deeper analysis of tumor biology and CAR T functionality
  • Contributes to external scientific discussions/research collaborations and publications and engagement with key opinion leaders in the field

Basic Qualifications

Doctorate and 2+ years of scientific experience

OR

Master’s and 6+ years of scientific experience

OR

Bachelor’s and 8+ years of scientific experience


Preferred Qualifications

  • Familiarity and experience with clinical and biomarker operations
  • Prior experience in Regulatory filings
  • Deep background in cancer immunotherapy, immunology and/or oncology with experience focusing on Multiple Myeloma
  • In-depth understanding of multiple myeloma, knowledge of clinical landscape, evolving therapy, competitive scenarios
  • Excellent understanding of clinical, translational, and mechanistic data
  • Understanding of early or late-stage drug and translational development process; including clinical trial experience in industry or academia
  • Familiarity with bioanalytical assay development and validation in a GxP environment
  • Experience working with engineered T cells, immunophenotyping, and NGS-based approaches to profile the function of tumor and immune cells
  • Comfortable in a matrixed and fast-paced company environment and able to adapt to changing priorities
  • Meaningful collaboration, excellent interpersonal and communication skills
  • Proficient with data presentations to communicate to a diverse cross-functional audience
  • Maintain a high degree of accuracy and attention to detail
  • Ph.D. degree in biology-related field (immunology, cancer biology, bioinformatics or a closely related field)

The work you do at Kite will help change how cancer is treated and ensure patients and their families have more time together. Ready to create more tomorrows with us? Hit apply.

#LI-ML1

#IND123


The salary range for this position is: $150,535.00 - $194,810.00. Kite considers a variety of factors when determining base compensation, including experience, qualifications, and geographic location. These considerations mean actual compensation will vary. This position may also be eligible for a discretionary annual bonus, discretionary stock-based long-term incentives (eligibility may vary based on role), paid time off, and a benefits package. Benefits include company-sponsored medical, dental, vision, and life insurance plans*.

For additional benefits information, visit:

https://www.gilead.com/careers/compensation-benefits-and-wellbeing

* Eligible employees may participate in benefit plans, subject to the terms and conditions of the applicable plans.


Kite is a biopharmaceutical company engaged in the development of innovative cancer immunotherapies with a goal of providing rapid, long-term durable response and eliminating the burden of chronic care. The company is focused on chimeric antigen receptor (CAR) and T cell receptor (TCR) engineered cell therapies designed to empower the immune system's ability to recognize and kill tumors. Kite is based in Santa Monica, CA. For more information on Kite, please visit www.kitepharma.com. Sign up to follow @KitePharma on Twitter at www.twitter.com/kitepharma.

For jobs in the United States:

As an equal opportunity employer, Gilead Sciences Inc. is committed to a diverse workforce. Employment decisions regarding recruitment and selection will be made without discrimination based on race, color, religion, national origin, gender, age, sexual orientation, physical or mental disability, genetic information or characteristic, gender identity and expression, veteran status, or other non-job related characteristics or other prohibited grounds specified in applicable federal, state and local laws. In order to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veterans' Readjustment Act of 1974, and Title I of the Americans with Disabilities Act of 1990, applicants who require accommodation in the job application process may contact ApplicantAccommodations@gilead.com for assistance.

For more information about equal employment opportunity protections, please view the 'Know Your Rights' poster.

NOTICE: EMPLOYEE POLYGRAPH PROTECTION ACT
YOUR RIGHTS UNDER THE FAMILY AND MEDICAL LEAVE ACT

PAY TRANSPARENCY NONDISCRIMINATION PROVISION

Our environment respects individual differences and recognizes each employee as an integral member of our company. Our workforce reflects these values and celebrates the individuals who make up our growing team.

Gilead provides a work environment free of harassment and prohibited conduct. We promote and support individual differences and diversity of thoughts and opinion.

For Current Kite Pharma Employees and Contractors:

Please log onto your Internal Career Site to apply for this job.