Job Description

Biology Scientists (In Vitro)
Job Number: 20-08093
 
Be part of a company that delivers life-changing healthcare solutions. Eclaro is looking for a Biology Scientists (In Vitro) for our client in Groton, CT.
 
Eclaro’s client is a leader in the Biopharmaceutical Industry, providing quality, innovative, and affordable medicines that make a difference in the lives of patients all over the world. If you’re up to the challenge, then take a chance at this rewarding opportunity!
 

Position Overview:
  • Responsible for execution of scientific research and/or scientific strategies in a biomarker/biomeasure focused flow cytometry laboratory.
  • Will provide technical and scientific support for biomarker data using flow cytometry (FACs), cell imaging and related technologies for both non-regulated and regulated preclinical and clinical biomarker studies supporting drug candidates.
 
Responsibilities:
  • Responsibilities for providing flow cytometry and cellular imaging data for biomarker/biomeasure discovery and development, supporting assay method development, validation and study execution.
  • Will participate with PDM teams and research units in a matrix environment.
  • Demonstrate experience in the delivery of flow cytometry and cell imaging-based biomarkers/biomeasures in animal and clinical studies, and have strong knowledge of biological systems, cellular functions and concepts in immunology to enable  discovery and development objectives.
  • Responsible for developing partnerships in a matrix environment, influencing project strategies, and providing expertise in technology development and implementation.
  • This role will participate in all phases of FACs laboratory operations including technology evaluations, the development of sample preparation, separation and detection methods, data analysis, interpretation, reporting and follow up discussions with the project teams on utilizing the data in appropriate decision making.
  • All colleagues in this role are responsible for maintaining regulatory compliance appropriate for clinical and preclinical study execution including all proscribed training as found in PDM SOPs and training transcripts. This includes knowledge, training and understanding of GLP/GCP guidance for execution of preclinical and clinical studies supporting portfolio projects as applicable.
  • Participate in continuous improvement of scientific and regulatory processes via update/creation of SOP’s, design and implementation of laboratory and study based processes, and development of best practices for bioanalytical data generation.
  • Responsible for QC and peer review of raw data, results, and final reports from other colleagues within the regulated group (depending on level of training).
  • Additionally responsible for participation in internal and external audits providing required information to auditors as needed.
  • May also participate/respond to internal audit findings on assigned projects.
 
Qualifications:
  • Should have multi-color flow cytometry experience
 
If hired, you will enjoy the following Eclaro Benefits:
  • 401k Retirement Savings Plan administered by Merrill Lynch
  • Commuter Check Pretax Commuter Benefits
  • Eligibility to purchase Medical, Dental & Vision Insurance through Eclaro
 
If interested, you may contact:
Paul Quibuyen
Christian.Quibuyen@eclaro.com
646-695-2942
Paul Quibuyen | LinkedIn
 

Equal Opportunity Employer: Eclaro values diversity and does not discriminate based on Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

Application Instructions

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