Principal Scientist - Translational Sciences

As a Principal Scientist - Translational Sciences at Syngene, your role will involve leading and executing clinical biomarker studies in a GLP/GCLP-compliant environment. Your responsibilities will include:

• Leading end-to-end biomarker study execution, including study planning, assay development, validation, sample analysis, data interpretation, and reporting.
• Developing, optimizing, and troubleshooting flow cytometry panels and NGS workflows.
• Ensuring full compliance with established SOPs, regulatory guidance, and data integrity requirements.
• Collaborating with Quality Control and Quality Assurance for study review, deviation management, and audit readiness.
• Mentoring junior scientists on biomarker assays, instrumentation, troubleshooting, and compliance best practices.

Specific requirements for this role include:

Experience

• Mid senior level experience in clinical biomarker assays within CRO, clinical research, or translational sciences environments.
• Hands-on expertise in clinical flow cytometry, NGS library preparation, and sequencing workflows.
• Proficiency with additional assay platforms such as qPCR, IHC, and ELISA.
• Experience working in GLP/GCLP and other regulatory-driven laboratory environments.

Skills and Capabilities:

• Advanced technical expertise in clinical flow cytometry.
• Technical expertise in RNA isolation, QC, and library preparation for NGS studies.
• Strong problem-solving skills and scientific rigor.
• Excellent organizational skills and ability to manage multiple studies.
• Effective communication and interpersonal skills.

Education

• Master's in molecular Biology, biotechnology, or translational sciences.

At Syngene, safety is a top priority, and you will be expected to adhere to safety guidelines, procedures, and SOPs at all times. Additionally, you will be part of a team that values excellence, integrity, and professionalism.

Syngene is committed to providing equal employment opportunities to all individuals, regardless of age, color, national origin, disability, race, religion, gender, sexual orientation, genetic information, marital status, veteran status, or any other characteristic protected by applicable legislation. Reasonable accommodations will be provided for qualified individuals with disabilities. As a Principal Scientist - Translational Sciences at Syngene, your role will involve leading and executing clinical biomarker studies in a GLP/GCLP-compliant environment. Your responsibilities will include:

• Leading end-to-end biomarker study execution, including study planning, assay development, validation, sample analysis, data interpretation, and reporting.
• Developing, optimizing, and troubleshooting flow cytometry panels and NGS workflows.
• Ensuring full compliance with established SOPs, regulatory guidance, and data integrity requirements.
• Collaborating with Quality Control and Quality Assurance for study review, deviation management, and audit readiness.
• Mentoring junior scientists on biomarker assays, instrumentation, troubleshooting, and compliance best practices.

Specific requirements for this role include:

Experience

• Mid senior level experience in clinical biomarker assays within CRO, clinical research, or translational sciences environments.
• Hands-on expertise in clinical flow cytometry, NGS library preparation, and sequencing workflows.
• Proficiency with additional assay platforms such as qPCR, IHC, and ELISA.
• Experience working in GLP/GCLP and other regulatory-driven laboratory environments.

Skills and Capabilities:

• Advanced technical expertise in clinical flow cytometry.
• Technical expertise in RNA isolation, QC, and library preparation for NGS studies.
• Strong problem-solving skills and scientific rigor.
• Excellent organizational skills and ability to manage multiple studies.
• Effective communication and interpersonal skills.

Education

• Master's in molecular Biology, biotechnology, or translational sciences.

At Syngene, safety is a top priority, and you will be expected to adhere to safety guidelines, procedures, and SOPs at all times. Additionally, you will be part of a team that values excellence, integrity, and professionalism.

Syngene is committed to providing equal employment opportunities to all individuals, regardless of age, color, national origin, disability, race, religion, gender, sexual orientation, genetic information, marital status, veteran status, or any other characteristic protected by applicable legislation. Reasonable accommodations will be provided for qualified individuals with disabilities.