Hi, I’m
Samantha Peck
Berlin,Connecticut
Summary
Highly experienced Biotech Executive with a strong scientific foundation, dedicated to leveraging my extensive background in program management, R&D product development, and laboratory operations to play a pivotal role in scientific decision-making processes within the biotech industry. Eager to contribute my expertise in driving innovation, ensuring regulatory compliance, and optimizing laboratory workflows to advance scientific initiatives and achieve transformative results.
Overview
11
years of professional experience
1
Certificate
Work History
IsoPlexis(PhenomeX)
Sr. Director of Program Management
10.2020 - Current
Job overview
- Established highly effective Program Management Office (PMO) comprising project managers proficient in overseeing diverse cross-functional projects encompassing services, product development, sustaining engineering, protocol development, software development, process optimization, and manufacturing operations.
- Developed and implemented comprehensive Standard Operating Procedures (SOPs), templates, software tools, and streamlined processes to govern PM function, resulting in enhanced project management efficiency and compliance.
- Collaborated directly with clients to conceptualize and design customized experimental frameworks for service projects, spanning from instrument demonstrations to large-scale clinical trials, showcasing exceptional client engagement and scientific acumen.
- Assumed leadership in managing end-to-end aspects of service projects, encompassing costing, contract drafting and execution, and meticulous laboratory coordination, ensuring successful project execution and client satisfaction.
- Served as primary scientific liaison, overseeing experimental planning, data report generation, and data review in close collaboration with clients, demonstrating strong client relationships and effective scientific communication.
- Developed intricate project tracking dashboards and dynamic presentation decks to comprehensively report on project status, timelines, resource allocation, budget adherence, and financial metrics. Regularly presented updates to senior leadership team, facilitating informed decision-making.
- Innovatively designed and implemented automated specimen tracking and workflow monitoring systems in SmartSheet, driving efficiency and accuracy across all laboratory projects.
- Managed a team of direct reports responsible for projects within diverse portfolios, providing leadership, guidance, and ensuring successful project outcomes.
- Conducted multi-departmental training sessions on project management and service-related topics, fostering knowledge sharing and strengthening project management capabilities across organization.
- Spearheaded establishment of integrated product development process following PhenomeX merger, contributing to organizational alignment and efficiency.
- Stepped in as interim head of scientific support department from June to November of 2021, demonstrating adaptability and leadership during critical period.
Sema4 Genomics (Formerly Mount Sinai)
Director of Clinical Project Management
05.2019 - 10.2020
Job overview
- Coordinated with cross-functional teams to resolve project issues and mitigate risks.
- Drafted project reports to identify successful outcomes, insights and future recommendations.
- Managed clinical oncology, virology, and clinical development portfolios.
- Managed direct reports who own projects within various portfolios.
- Continue to manage individual projects from conception through validation/launch.
- Worked closely with product and GM teams to facilitate commercial launch of new products.
- Managed documentation and submission requirements for various regulatory bodies including NYSDOH and FDA.
Sema4 Genomics (Formerly Mount Sinai)
Project Manager/Sr. Project Manager
01.2017 - 05.2019
Job overview
- Managed multiple cross-functional, multi-site projects from design to delivery, including clinical development/validations, large-scale research projects for external clients, and internal operational optimizations.
- Developed detailed work plans, defined major milestones, identified key project risks, established and maintained project timelines, and determined budgets to ensure successful project execution.
- Managed all aspects of sample management for development and validation projects, including commercial vendor sourcing, cost comparison, purchasing, and tracking of sample information.
- Collaborated with finance, purchasing, and lab teams to create comprehensive costing models, aiding in validation budgets, per-sample production costs, and cost estimates for large research projects.
- Conducted research on commercial assay options for various company initiatives, providing cost and utility comparisons to inform decision-making.
- Contributed to optimization of various lab workflows, including RNA QC and FFPE extraction, to enhance efficiency and accuracy.
- Served as interim Accessioning Manager from February to July of 2018, overseeing critical aspects of accessioning process.
- Worked closely with lab team, bioinformatics specialists, and lab directors to define and execute necessary experiments for assay development, familiarization, optimization, and validation.
The Jackson Laboratory
Clinical Genomic Technologist II
02.2015 - 01.2017
Job overview
- Designed and executed optimization experiments to enhance Turnaround Time (TAT) and quality of laboratory workflows, resulting in improved efficiency and accuracy.
- Processed clinical patient specimens in strict adherence to all CLIA/CAP guidelines, ensuring highest standards of quality and compliance.
- Performed end-to-end processing for multiple Next-Generation Sequencing (NGS) workflows, handling both DNA and RNA specimens with precision.
- Ran scripts to manually generate fastq files, monitored sequencing metrics, and initiated analysis pipelines, contributing to generation of valuable genomic data.
- Authored Standard Operating Procedures (SOPs) for molecular assays, NGS sequencing platforms, and various laboratory equipment, ensuring standardized protocols and compliance.
- Implemented cell culture techniques to cultivate cells with relevant mutations for use in assay validations, enabling more accurate and reliable testing.
- Designed, executed, and managed projects to validate assays and test systems, meticulously following CLIA/CAP guidelines to maintain regulatory compliance.
- Acted as equipment manager, overseeing tracking, scheduling, and performance of preventative maintenance and calibrations for all laboratory equipment, ensuring equipment reliability and compliance with CLIA/CAP standards.
Yale Center For Genome Analysis
Research Assistant I
02.2013 - 02.2015
Job overview
- Proficiently conducted end-to-end processing for both RNA and DNA Next-Generation Sequencing (NGS) workflows, managing high volume of up to 200 samples per week.
- Meticulously processed clinical patient specimens, strictly adhering to all CLIA/CAP guidelines to ensure highest standards of sample handling and quality.
- Conducted comprehensive quality and quantity assessments for DNA specimens, contributing to accurate and reliable data generation.
- Demonstrated leadership skills by assuming role of lead technician during extended absence of direct manager, effectively managing workflow and team responsibilities.
- Played pivotal role in training new research assistants, providing comprehensive instruction on all aspects of whole exome library preparation workflow, ensuring smooth onboarding and knowledge transfer.
- Consistently maintained compliance with CLIA/CAP guidelines while processing clinical patient specimens, prioritizing accuracy and regulatory adherence.
- Worked both independently and collaboratively in fast-paced laboratory environment.
- Performed statistical, qualitative, and quantitative analysis.
Education
Quinnipiac UniversityHamden, CT
Master of Science from Biomedical Laboratory Sciences
05.2014
Clark UniversityWorcester, MA
Bachelor of Arts from Biochemistry And Molecular Biology
12.2011
Skills
- Program Management
- Vendor Management
- R&D Product Development
- Molecular Assay Implementation
- Regulatory Compliance (CLIA/CAP)
- Sample Management
- Laboratory Workflow Optimization
- Quality Control
- Team Leadership and Training
- Equipment Management
- Data Analysis and Interpretation
Certification
- PMP - Project Management Professional (PMI)-2018
Timeline
Sr. Director of Program Management
IsoPlexis(PhenomeX)
10.2020 - Current
Director of Clinical Project Management
Sema4 Genomics (Formerly Mount Sinai)
05.2019 - 10.2020
Project Manager/Sr. Project Manager
Sema4 Genomics (Formerly Mount Sinai)
01.2017 - 05.2019
Clinical Genomic Technologist II
The Jackson Laboratory
02.2015 - 01.2017
Research Assistant I
Yale Center For Genome Analysis
02.2013 - 02.2015
Quinnipiac University
Master of Science from Biomedical Laboratory Sciences
Clark University
Bachelor of Arts from Biochemistry And Molecular Biology
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