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You will be updated with latest job alerts via email$ 102900 - 171500
1 Vacancy
POSITION SUMMARY
This position will sit within the Assay Development Group of the Companion Diagnostic Center of Excellence supporting clinical biomarker and diagnostic strategy development through scientific and technical oversight of biomarker and prototype diagnostic assays clinical implementation and management of external and internal partners in oncology and other therapeutic will bring technical leadership to devise scientifically sound biomarker and diagnostic testing strategies effective implementation of assays into clinical trials and communicating data and program impacts to key stakeholders and project teams.
KEY RESPONSIBILITIES:
Provide bio-analytical assay technical and operational expertise to Study Teams to ensure delivery of high-quality clinical biomarker and Diagnostic (Dx) data
Support assay development and timely availability of fit-for-purpose and Dx clinical biomarker assays to clinical Study Teams
Function as key point of contact with external and internal clinical labs with oversight responsibilities for agreements work plans budget and invoices assay development transfer validation and associated report sample analyses and associated report data transfers and overall data quality
Provide technical support for selection qualification and periodic audits of bioanalytical laboratories supporting oncology clinical trial biomarker and Dx assays as appropriate
Collaborate with Study Teams to ensure appropriate biomarker and Dx sample handling and processing steps are appropriately performed during clinical trials
Serve as subject matter expert for biomarker testing technologies (NGS PCR IHC flow cytometry immuno-assays etc)
Collaborate with Asset Teams to manage the timely testing of clinical trial samples and the analysis and reporting of the associated data
MNIMUM QUALIFICATIONS
PhD in a relevant scientific field (e.g. pathology immunology oncology molecular biology genetics) OR
MS in a relevant scientific field (e.g. pathology immunology oncology molecular biology genetics) with 2 years of relevant experience
Experience with the research and development of biologic therapeutics biomarker assay development validation and execution in clinical trials
Experience and expertise in biomarker selection trials
An understanding of translational approaches as applied to clinical trial design and regulatory processes proof-of-concept studies and the implementation of biomarkers and Dx
Development validation and implementation of a broad range of platform technologies within clinical trials (e.g. NGS IHC PCR FISH flow cytometry other cell based and circulating biomarker technologies)
Demonstrated understanding of clinical laboratory regulatory and compliance requirements (GLP GCP GCLP CLIA CAP)
Demonstrated ability to think strategically and creatively while contributing to multiple projects simultaneously
Experience working productively in a collaborative multi-disciplinary and diverse team setting
Excellent communication and organizational skills; able to convey complex scientific and business issues to devise reach agreement on and implement solutions
Experience collaborating leading influencing and motivating others
PREFERRED QUALIFICATION
CRO management and outsourcing engagement expertise
Work Location Assignment:On Premise
Relocation assistance may be available based on business needs and/or eligibility.
Sunshine Act
Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations. These laws and regulations require Pfizer to provide government agencies with information such as a health care providers name address and the type of payments or other value received generally for public disclosure. Subject to further legal review and statutory or regulatory clarification which Pfizer intends to pursue reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act. Therefore if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse your name address and the amount of payments made currently will be reported to the government. If you have questions regarding this matter please do not hesitate to contact your Talent Acquisition representative.
EEO & Employment Eligibility
Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race color religion sex sexual orientation age gender identity or gender expression national origin disability or veteran status. Pfizer also complies with all applicable national state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Pfizer is an E-Verify employer. This position requires permanent work authorization in the United States.
Required Experience:
Manager
Full-Time