Exelixis

Senior Scientist II (Preclinical Bioanalysis)

Exelixis$132K — $188K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Master's or PhD in analytical chemistry, biology, or related discipline required
  • 7+ years of relevant experience with a Master's or 2+ years with a PhD preferred
  • Hands-on experience with LCMS-based bioanalytical assays for biologics
  • Scientific understanding of PK and PD concepts in cancer biology
  • Demonstrated drive for scientific excellence and problem-solving abilities

Responsibilities

  • Design and execute assays for ADCs and biologics in various matrices
  • Manage pharmacokinetic studies with CROs and in-house
  • Analyze and interpret critical scientific data
  • Collaborate with internal teams for timely project advancement
  • Communicate scientific concepts to multidisciplinary teams
  • Contribute to translational biology efforts
  • Ensure compliance with intellectual property and safety policies

Benefits

  • 401k plan with generous contributions
  • Group medical, dental, and vision coverage
  • Life and disability insurance
  • Flexible spending accounts
  • Opportunity to purchase company stock
  • Discretionary annual bonus program
  • 15 vacation days, 17 paid holidays, and 10 sick days annually
Full Job Description
SUMMARY/JOB PURPOSE:

The Senior Scientist II of preclinical bioanalysis provides preclinical bioanalytical support for the advancement of the biologics portfolio at Exelixis. The incumbent must have strong LCMS-based bioanalysis experience as s/he supports preclinical activities of ongoing and new projects in antibody drug conjugates and other biologics.

ESSENTIAL DUTIES AND RESPONSIBILITIES:
  • Independently design and execute assay development and qualification of ADCs or other biologics in rodent and NHP matrices, perform pharmacokinetic sample analyses in support of proof-of-concept studies on biologic oncology programs from discovery to lead selection.
  • Design, implement and manage studies for pharmacokinetic characterization of biologic drug candidates conducted by CROs and in-house as needed.
  • Critical scientific/technical data analysis and interpretation of experiments.
  • Interact and collaborate with internal departments to deliver quality and timely findings in support of drug candidate advancement.
  • Effectively communicate scientific concepts, findings, and interpretation to multi-disciplinary teams.
  • Contribute to other translational biology efforts
  • Follow company intellectual property and compliance policies and practices.
  • Comply with company health and safety policies and general laboratory practices.


SUPERVISORY RESPONSIBILITIES:
  • Directing work to a CRO, Consultant, or 3rd party as necessary


EDUCATION/EXPERIENCE/KNOWLEDGE & SKILLS:

Education:
• Master's degree in analytical chemistry or biology or closely related discipline and a minimum of seven (7) years of related experience; or
• PhD degree in analytical chemistry or biology or closely related discipline and a minimum of two (2) years of related experience is preferred; or
• Equivalent combination of education and experience.

Experience:
  • Hand-on experience in assay development and sample analysis with LCMS-based bioanalytical assays for biologics is essential.
  • Scientific understanding of in vitro and in vivo pharmacology, PK, and PD concepts in cancer biology is important.


Knowledge/Skills:
  • Demonstrated drive for rigorous scientific excellence. Ability to think critically and creatively to identify and solve scientific problems.
  • Knowledge and familiarity in LC-MS-based bioanalysis is critical
  • Ability to work independently, good time management and organization skills.
  • Knowledge and experience of ligand-binding assays and metabolite ID is a plus
  • Excellent written, oral, and interpersonal communication skills.
  • A strong team player.
  • Advanced knowledge in Excel, Word, PowerPoint, PDF, GraphPad prism.
  • Good tracking record and report writing.


WORKING CONDITIONS:
• Environment: primarily working in laboratories or in office
• Exposures encountered, such as hazardous materials, and extreme cold.
• Travel required (up to 10%)

#LI-HG1

Our compensation reflects the cost of labor across several U.S. geographic markets, and we pay differently based on those defined markets. The base pay range for this position is $132,500 - $188,000 annually. The base pay range may take into account the candidate's geographic region, which will adjust the pay depending on the specific work location. The base pay offered will take into account the candidate's geographic region, job-related knowledge, skills, experience and internal equity, among other factors.

In addition to the base salary, as part of our Total Rewards program, Exelixis offers comprehensive employee benefits package, including a 401k plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts. Employees are also eligible for a discretionary annual bonus program, or if field sales staff, a sales-based incentive plan. Exelixis also offers employees the opportunity to purchase company stock, and receive long-term incentives, 15 accrued vacation days in their first year, 17 paid holidays including a company-wide winter shutdown in December, and up to 10 sick days throughout the calendar year.

DISCLAIMER
The preceding job description has been designed to indicate the general nature and level of work performed by employees within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities and qualifications required of employees assigned to the job.

About Exelixis

Exelixis is a biotechnology company that develops and commercializes innovative medicines for the treatment of cancer. The company's flagship product, CABOMETYX® (cabozantinib), is an inhibitor of multiple tyrosine kinases, including MET, AXL, and VEGFR, which are involved in the growth and spread of cancer cells. CABOMETYX is approved in the United States for the treatment of advanced renal cell carcinoma (RCC) and hepatocellular carcinoma (HCC), and is also approved in the European Union and other countries for the treatment of advanced RCC. Exelixis is headquartered in Alameda, California, and has additional offices in South San Francisco, California, and Basel, Switzerland. Learn more at www.exelixis.com.
Learn more about Exelixis
Size
954 employees
Market Cap
$5 billion
Industry
Net Income
$111.7 million
5 Year Trend
+49.6%
Revenue
$987.5 million
NASDAQ

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