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Clinical Affairs Scientist

Employer
Agilent Technologies
Location
Preferred location is Carpinteria, CA but will consider remote work for well qualified candidates.
Start date
Oct 22, 2019

View more

Discipline
Clinical
Required Education
Bachelors Degree
Position Type
Full time

Job Details

Agilent inspires and supports discoveries that advance the quality of life. We provide life science, diagnostic and applied market laboratories worldwide with instruments, services, consumables, applications and expertise. Agilent enables customers to gain the answers and insights they seek ---- so they can do what they do best: improve the world around us. Information about Agilent is available at www.agilent.com.

In the Companion Diagnostics Business (CDx), our team partners very closely with leading pharmaceutical companies to develop, manufacture and commercialize highly regulated medical devices which are critical for physicians to help select therapies for their patients.

Become a part of a growing and dedicated team that does truly inspiring work in the field of Precision Medicine. Our employees are passionate about their contributions because there is a very direct connection to helping patients with cancer.

We are searching for an experienced Clinical Affairs Scientist to work within the exciting field of oncology Companion Diagnostics (CDx). As a Clinical Affairs Scientist, your main responsibilities will be to determine clinical strategy in conjunction with team members, write clinical protocols, analyze data and write reports to support the clinical documentation of Companion Diagnostics (CDx)in the field of tissue-based Cancer Diagnostics. This position requires strong support to regulatory applications and scientific marketing activities. The top candidate will have a strong background in biostatistics and experience working in oncology drug, biomarker or in vitro diagnostic clinical development. The candidate will work directly with pharmaceutical partners, clinical and R&D scientists, Clinical Trial Managers and regulatory affairs to assure compliance with internal and external requirements.

Responsibilities include but are not limited to:

  • Contribute to the clinical strategy for CDx products.
  • Interact and communication with pharmaceutical partners, both domestic and international
  • Regulary interact with regulatory bodies, such as the FDA
  • Write and interpret clinical protocols, reports and provide data analysis
  • Provide leadership and direction to the clinical affairs scientific staff
  • High work capacity may be required at certain times in high priority projects

Preferred location is Carpinteria, CA but will consider remote work for well qualified candidates. 

Required Qualifications:

  • Bachelor's or University degree or equivalent in pharmaceutical, medical or other relevant biological science
  • 4+ years' experience authoring protocols and reports for diagnostic, medical device or pharmaceutical industry
  • Experience designing clinical studies
  • Experience working with external partners and regulatory bodies including the FDA
  • A solid knowledge of biostatistics and Good Clinical Practice
  • Experience in working in parallel projects teams
  • Advanced skills in both written and spoken communication

Preferred Qualifications:

  • Experience working in oncology and/or pathology
  • Advance degree in pharmaceutical, medical or other relevant biological science

Preferred location is Carpinteria, CA but will consider remote work for well qualified candidates.

Agilent Technologies, Inc. is an Equal Employment Opportunity and Affirmative Action employer. We value diversity at all levels. All individuals, regardless of personal characteristics, are encouraged to apply. All qualified applicants will receive consideration for employment without regard to sex, pregnancy, race, religion or religious creed, color, gender, gender identity, gender expression, national origin, ancestry, physical or mental disability, medical condition, genetic information, marital status, registered domestic partner status, age, sexual orientation, military or veteran status, protected veteran status, or any other basis protected by federal, state, local law, ordinance, or regulation and will not be discriminated against on these bases.

Agilent Technologies, Inc., is committed to diversity in the workplace and strives to support candidates with disabilities. If you have a disability and need assistance with any part of the application or interview process or have questions about workplace accessibility, please contact +1-262-754-5030 email job_posting@agilent.com. EOE AA M/F/Vet/Disability/Sexual Orientation/Gender Identity.

For more information about equal employment opportunity protections, please see all of our notices for EEO below.

https://www.dol.gov/ofccp/regs/compliance/posters/pdf/eeopost.pdf,

https://www.dol.gov/ofccp/regs/compliance/posters/pdf/OFCCP_EEO_Supplement_Final_JRF_QA_508c.pd

Company

Premier Laboratory Partner for a Better World

Analytical scientists and clinical researchers worldwide rely on Agilent to help fulfill their most complex laboratory demands. Our instruments, software, services, and consumables address the full range of scientific and laboratory management needs—so our customers can do what they do best: improve the world around us.

Whether a laboratory is engaged in environmental testing, academic research, medical diagnostics, pharmaceuticals, petrochemicals, or food testing, Agilent provides laboratory solutions to meet their full spectrum of needs. We work closely with customers to help address global trends that impact human health and the environment and to anticipate future scientific needs. Our solutions improve the efficiency of the entire laboratory, from sample prep to data interpretation and management.

Customers trust Agilent for solutions that enable insights...for a better world.

Company info
Website
Phone
+1 916-985-7888
Location
91 Blue Ravine Rd
Folsom
California
95630
US

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