Supports the NC Water Safety Act through study design, monitoring coordination, sampling method development, and sample transport for statewide PFAS and other contaminant monitoring.
Locations (3)
Raleigh, North Carolina, United States
Mooresville, North Carolina, United States
Winston-Salem, North Carolina, United States
Compensation
Recruitment Range: $52,592.00 - $72,314.00
Responsibilities
Sampling and sample transport, including site visits, coordinating sample preservation conditions, and coordinating delivery of samples to Collaboratory academic institutions
Facilitating communication and coordination between DEQ staff, NPDES permitted dischargers, and the universities involved in the NC Collaboratory; managing conversations in person, electronically, and by telephone
Collaborating closely with existing programs to maximize sample collection efficiency and accuracy of data for water quality standards development, assessment, and emergency response
Training internal NCDEQ staff and external public and private entities on Standard Operating Procedures (SOPs) for water and wastewater sampling for PFAS and other analytes
Auditing sampling proficiency to ensure consistent sample quality and data collection throughout the study
Requirements
Bachelor's degree in one of the agricultural, biological, engineering, environmental, or natural resource sciences or a closely related curriculum from an appropriately accredited institution
Responsible for developing scientific background, methodology, and grant proposals for Health Services and Informatics Research at Parkview Research Center.
Responsibilities
Develop scientific background and methodology for external and internal funding proposals
Collaborate with health services research team to execute study protocols
Lead data analysis of research findings
Develop rigorous program evaluation, study protocols and grant proposals
Secure external grant funding
Requirements
PhD in a field applicable to health services research (e.g., Health Informatics, Computer Science, Psychology, Human-Computer Interaction, Social Computing)
Nice to have: post-doctoral fellowship experience
Nice to have: prior work experience in a healthcare environment
The Research Program Manager, Investigator-Initiated Studies serves as the primary program management lead and faculty-facing partner for investigator-led research studies managed through the Division of Institutional Research.
Responsibilities
Provide end-to-end support from early concept development and grant strategy through study activation, execution, and closeout
Partner with investigators to translate scientific questions into feasible study designs
Identify relevant funding opportunities and support grant submissions
Facilitate protocol and grant development by connecting investigators with biostatisticians, regulatory affairs, data managers, and other subject matter experts
Conduct initial needs assessments and develop study-specific project plans, timelines, and milestone trackers
Requirements
Bachelor's in a life science, health science, epidemiology, public health, or related field
Master's or PhD, or equivalent advanced degree in a life science, health science, clinical research, or public health field
Provide statistical support for assigned clinical studies under the guidance of the Biometrics/Biostatistics Team Lead or other senior statistical leadership.
Compensation
Target Base Pay Range: $116,000.00 - $151,000.00
Responsibilities
Provide statistical support for assigned clinical studies under the guidance of the Biometrics/Biostatistics Team Lead or other senior statistical leadership.
Collaborate with clinical, data management, statistical programming, and other cross-functional team members to support study activities.
Contribute statistical input to study design, protocol development, endpoint definition, and analysis planning.
Prepare and review assigned statistical analysis plans, case report forms, clinical database specifications, validation plans, table, figure, and listing shells, analysis dataset specifications, and related documentation.
Perform statistical analyses, simulations, and ad hoc analyses as needed.
Requirements
Master's degree in Statistics, Biostatistics, or related field
Ph.D. preferred
Nice to have: R or other statistical software
Nice to have: experience with external vendors or contract research organizations
The Clinical Development Medical Director is responsible for medical and scientific oversight, data integrity, and quality of clinical trials in Internal Medicine, with direct responsibility for clinical deliverables for one or more studies.
Compensation
The annual base salary for this position ranges from $239,900.00 to $399,800.00. In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 25.0% of the base salary and eligibility to participate in our share based long term incentive program.
Responsibilities
Provides medical monitoring on one or more clinical trials
Provides timely, study-related medical information and guidance
Contributes to medical assessments of Quality Events
Conducts and documents periodic safety data review and ongoing clinical/medical data review
Reviews Required Safety Text for the Informed Consent Document
Requirements
Medical degree (MD, DO, MBBS, MBChB)
Licensed to prescribe medicines independent of supervision
Lead CX research and methodology for Away From Home product initiatives, translating consumer insights into product and packaging decisions.
Compensation
New Hire Base Salary Range: $104,200.00 - $130,200.00
Bonus: This position is eligible for a performance-based bonus as provided by the plan terms and governing documents.
Responsibilities
Provide CX technical leadership for the Away From Home team
Serve as subject matter expert for product and packaging design consumer research
Architect end-to-end CX learning plans
Translate complex consumer experience insights into actionable requirements
Lead high-stakes stakeholder readouts
Requirements
Bachelor’s degree minimum (Consumer Behavior, Psychology, Marketing Research, Engineering, Food Science, Human Factors, Industrial Design, or related STEM field)
Senior Data Scientist partnering with assay development, lab operations, quality, regulatory, and software teams to support early cancer detection assays.
Responsibilities
Design studies and analyze data to evaluate assay performance
Develop statistical methods for production monitoring and qualifying reagents, controls, and instruments
Assess impact of reagent, instrument, software, and process changes and design bridging studies
Support verification and transfer to production for LDT and IVD products
Support regulatory submissions with rigorous analyses
Requirements
Master’s degree in Statistics, Biostatistics, Applied Math, Bioinformatics, Engineering, or related quantitative field; PhD preferred
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