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
Lead global clinical programs in late respiratory and immunology, overseeing study design, execution, and regulatory interactions.
Compensation
The annual base salary for this position ranges from $288,059 - $432,088. However, base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. In addition, our positions offer a short-term incentive bonus opportunity; eligibility to participate in our equity-based long-term incentive program.
Responsibilities
Design and conduct clinical studies
Develop protocols, statistical analysis plans, and safety monitoring plans
Ensure compliance with GCP and regulatory requirements
Manage risk mitigation strategies
Represent program at regulatory and ethics meetings
Requirements
M.D., Ph.D., or equivalent medical or scientific qualification
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
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
Lead clinical research, design and execution of studies for Myant's e-textile health technologies.
Responsibilities
Design, plan and run clinical and human-subject studies
Develop and amend protocols, consent forms and study documents
Manage REB submissions, amendments and renewals
Analyze and interpret clinical and user research data
Lead scientific abstracts, manuscripts, white papers and conference presentations
Requirements
Master's or PhD degree in Clinical Sciences, Health Sciences, Biomedical Sciences, Kinesiology, Rehabilitation Sciences, Biomedical Engineering or related discipline
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Senior Vice President, Late-Stage Clinical DevelopmentRevolution Medicines · Redwood City, US
Clinical ScientistMyant Shared Service Corp. · Mississauga, Canada