Job Description

Biology Scientists (In Vitro)
Job Number: 21-09365
 
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 among the world’s largest pharmaceutical companies, trusted by billions to provide superior, cutting-edge, and inexpensive medicine that improves health and well-being. If you’re up to the challenge, then take a chance at this rewarding opportunity!
 
Position Overview:
  • The Regulated Clinical Biomarker/Flow Cytometry group works with clinical and translational teams across Pharmaceutical research units to develop and implement complex flow cytometry-based biomarker assays and supportive translational/mechanistic studies for early phase clinical projects in a GCLP environment.
  • This position is responsible for execution of scientific research and/or scientific strategies in a biomarker/biomeasure focused flow cytometry laboratory.
  • This scientist will provide technical and scientific support for biomarker data using flow cytometry (FACs), cell imaging and related technologies for both non-regulated and regulated clinical biomarker studies supporting Pharmaceutical drug candidates.
  • This scientist will interact with inter-departmental colleagues, clinical and translational teams, research units and contract research organizations in a matrixed environment.
 
Responsibilities:
  • Responsible for clinical flow cytometry biomarker assay development and validation, data generation and analysis, QC, data interpretation and communication to project teams to enable appropriate decision making
  • This position will participate with ECD teams and research units in a matrix environment. The person will demonstrate experience in the delivery of flow cytometry and cell imaging-based biomarkers/biomeasures in clinical studies, and have strong knowledge of biological systems, cellular functions and concepts in immunology to enable Pharmaceutical 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 study execution including all proscribed training as found in ECD SOPs and training transcripts. This includes knowledge, training and understanding of GLP/GCP guidance for execution of preclinical and clinical studies supporting Pharmaceutical 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
  • Occasional weekend work for processing clinical samples should be anticipated
 
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:
Chris Imbien
Chris.Imbien@eclaro.com
843-872-9257
 
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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