Accountable for the medical & scientific integrity of the study and the wellbeing of patients enrolled in one or more clinical trials, ensuring the design of efficient and high-quality clinical trials.
Compensation
The annual base salary for this position ranges from $189,200.00 to $315,400.00. In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 22.5% of the base salary and eligibility to participate in our share based long term incentive program.
Responsibilities
Performs medical monitoring on one or more clinical trials
Provides study-related medical information and assistance to investigators, site personnel, and non-study health care providers
Handles safety findings, medical issues, and complex serious adverse events
Conducts and documents periodic safety data reviews and ongoing clinical/medical data review
Reviews required safety text and endorses significant medical changes in the Informed Consent Document
Senior manager overseeing scientific oversight, data integrity, and quality of clinical trials in Internal Medicine.
Compensation
The annual base salary for this position ranges from $139,100.00 to $231,900.00. In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 17.5% of the base salary and eligibility to participate in our share based long term incentive program.
Responsibilities
Provides clinical support for studies
Contributes to protocol design and amendments
Supports study team in protocol review governance
Develops informed consent documents
Provides input to statistical analysis plan
Requirements
PhD, PharmD, or equivalent
MA/MS with at least 5 years
BA/BS with at least 6 years of Clinical Research experience
Provide applications support across multiple scientific subject areas, including drug discovery and genomics, and act as the direct contact for customers regarding scientific and application-related questions.
The RN Study Coordinator is accountable for the coordination and delivery of nursing care, including direct patient care, research participant/family education in clinical and research settings.
Responsibilities
Coordinate and deliver nursing care
Provide direct patient care
Educate research participants and families
Design, organize, and monitor protocols
Assist with grant applications, abstracts, posters, and manuscripts
Lead cardiovascular medical science and strategy for PPD clinical research business, driving RFP quality, strategic alliances, and clinical development expertise.
Locations (2)
Raleigh, North Carolina, United States
United States
Compensation
Competitive salary and benefits
Responsibilities
Ensure high-quality input into RFPs including strategy, regulatory, drug class, protocol and safety considerations
Provide therapeutic and developmental expertise to internal teams and clients
Support bid defenses and client governance
Develop and review regulatory documents such as Investigator Brochure, NDA/MAA packages
A Director-level role responsible for scientific oversight, data integrity, and quality of clinical trials in Internal Medicine, managing clinical deliverables and teams.
Compensation
The annual base salary for this position ranges from $176,600.00 to $294,300.00
Responsibilities
Independently leads clinical execution of one or more studies
Provides input to protocol design document and leads development of protocol, amendments, and letters
Represents the study team in internal protocol review governance submissions
Partners with the Global Development Lead in study and disease area strategy
Ensures development of Study Informed Consent Documents and responses to external stakeholders
The annual salary range OR the hourly range for this role is $95,000.00 - $115,000.00.
Responsibilities
Provide applications support across multiple scientific subject areas, including drug discovery and genomics.
Understand the scope of customer projects and build, adapt, implement, and optimize liquid handling and automation protocols to improve customer workflows.
Provide customer training and support; maintain positive customer relations.
Support sales targets by partnering with the commercial team to provide high-level scientific and technical expertise.
Troubleshoot and diagnose technical problems and serve as a liaison with service and internal customer support teams.
Requirements
Bachelor’s degree in Life Science or related field of study
Nice to have: Advanced programming of laboratory automation workflows
Nice to have: Technical or application support within a Life Science company
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