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Scientist Senior Associate

Thousand Oaks, CA
“This Company requires all staff, staff augmentation external workers, and certain other external workers, in the United States and Puerto Rico vaccinated from COVID 19 as a condition of assignment at this company. In accordance with applicable law, this company will provide reasonable accommodations staff augmentation external workers qualify on the basis of a medical reason or a sincerely held religious belief, practice, or observance. Such accommodation may not pose an undue hardship this company, its operations, or its staff.”
    
Top 3 Must Have Skill Sets:    
        
Need in vitro experience
Need basic PCR/ DNA/ RNA experiment experience
Need cell line and tissue culture experience

Live-cell experience a plus
Metabolic / cardiovascular experience a plus

Day to Day Responsibilities:    

To perform experiments, organize data and analyze results under minimal supervision. With minimal supervision, plans, conducts or monitors experiments, records and organizes data, analyses results, generates robust and reliable data and/or Ensures that contracted studies are conducted in compliance with the respective protocol and applicable guidelines and regulations.Responsibilities include:
Monitors or follows established experimental design and protocols and performs routine tasks and studies to obtain reproducible and reliable results with limited supervision.
Plans, monitors or conducts, analyzes and records experiments, and provides interpretation of data.
Effectively transfers experimental methods from literature to the lab and makes modifications as necessary.
Develops and implements new protocols with moderate review.
Engages coworkers in scientific discussions.
Communicates data and interpretation to work group.
Skilled at developing systems to ensure quality data.
Skilled and/or knowledgeable in the use of standard laboratory equipment and with one or more major laboratory instruments/techniques.
Effectively trouble-shoots equipment and experimental difficulties.
Contributes to internal/external reports, papers, presentations, regulatory documents, invention disclosure submissions and/or patents.
Participates in department-wide support efforts such as safety, recruiting and committees.
May train staff and/or supervise others.
Coordinates and organizes resources needed to complete the task.
Understands when to seek input and when to make independent judgments; Skills: ; degree in Biology, Biochemistry or Analytical Chemistry; experience in a Biopharmaceutical working environment    

"This posting is for Contingent Worker, not an FTE"

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