Clinical Flow Cytometry Scientist - Pioneer Data Systems
Groton, CT 06340-5146
About the Job
Position Details:
Our client, a world-leading Pharmaceutical Company in Groton, CT is currently looking for an Flow Cytometry Scientist to join their expanding team.
Job Title: Flow Cytometry Scientist / Pharma Industry
Duration: 18 months contract, extendable up to 36 months
Location: Groton, CT
Note:
The client has the right-to-hire you as a permanent employee at any time during or after the end of the contract.
You may participate in the company group medical insurance plan
Job Description:
Job Title: Clinical Flow Cytometry Scientist
Summary:
The Regulated Clinical Biomarker/Flow Cytometry group works with clinical and translational teams across Client 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 the 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 Client 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
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 Client 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 collogues 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:
Bachelor's degree with a minimum of 3+ years of laboratory experience (can be educational experience)
Demonstrated experience in the delivery of flow cytometry and cell imaging-based biomarkers/biomeasures in clinical studies
Strong knowledge of biological systems, cellular functions and concepts in immunology
Prior flow cytometry experience preferred
Clear communication skills required
GCLP experience preferred
Location:
This is a fully onsite role in Groton, CT
Monday - Friday; 1st shift (occasional weekend work for processing clinical samples should be anticipated)
Our client, a world-leading Pharmaceutical Company in Groton, CT is currently looking for an Flow Cytometry Scientist to join their expanding team.
Job Title: Flow Cytometry Scientist / Pharma Industry
Duration: 18 months contract, extendable up to 36 months
Location: Groton, CT
Note:
The client has the right-to-hire you as a permanent employee at any time during or after the end of the contract.
You may participate in the company group medical insurance plan
Job Description:
Job Title: Clinical Flow Cytometry Scientist
Summary:
The Regulated Clinical Biomarker/Flow Cytometry group works with clinical and translational teams across Client 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 the 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 Client 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
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 Client 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 collogues 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:
Bachelor's degree with a minimum of 3+ years of laboratory experience (can be educational experience)
Demonstrated experience in the delivery of flow cytometry and cell imaging-based biomarkers/biomeasures in clinical studies
Strong knowledge of biological systems, cellular functions and concepts in immunology
Prior flow cytometry experience preferred
Clear communication skills required
GCLP experience preferred
Location:
This is a fully onsite role in Groton, CT
Monday - Friday; 1st shift (occasional weekend work for processing clinical samples should be anticipated)
Source : Pioneer Data Systems
