Job Details

ID #2634162
Estado Connecticut
Ciudad Groton
Full-time
Salario USD TBD TBD
Fuente Pfizer
Showed 2019-08-18
Fecha 2019-08-19
Fecha tope 2019-10-18
Categoría Etcétera
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Senior Associate Scientist, Global Clinical Pathology

Connecticut, Groton 00000 Groton USA

Vacancy caducado!

This position will reside within the Global Clinical Pathology laboratory a section of the Global Biomarker Laboratories within Drug Safety Research and Development The candidate will contribute to the Global DSRD Biomarker Clinical Pathology group to enable effectiveness across the DSRD Global Biomarker organization. ROLE SUMMARYPfizer is excited to present an opening for a Senior Associate Scientist in our Global Clinical Pathology group. The Clinical Pathology laboratory is a highly innovative, functional and integrated scientific discipline contributing to the advancement of the Pfizer portfolio. It is a section of the Global Biomarker Laboratories within Drug Safety Research and Development. The selected candidate will contribute to the Global DSRD Biomarker Clinical Pathology group to enable effectiveness across the DSRD Global Biomarker organization. The role will provide laboratory support for the Global Clinical Pathology laboratory including routine Clinical Pathology and investigative biomarker support for the efficacy and safety evaluation of drug candidates in discovery, pre-clinical, and clinical studies. Routine clinical pathology analysis involves hematology, clinical chemistry, coagulation, immunoassay and urinalysis.ROLE RESPONSIBILITIESIn this role you will be responsible for generation of hematology, clinical chemistry, urinalysis, coagulation, immunoassay and novel assay development data in support of both safety and efficacy assessment of pharmaceutical drug candidates in compliance with GLP/GCLP and CLIA regulatory standards as applicable within a Clinical Pathology laboratory. Other responsibilities include:

Ensuring the generation of the highest quality of Clinical Pathology raw data, contributing to methodology development for new biomarkers and contributing to technology development

Author technical documents such as validation plans and summaries, Standard Operating Procedures (SOPs), and User Guides where appropriate

Exposure to new methods development such as flow cytometry and plate base assays is possible based upon individual experience and knowledge

Experience with a laboratory informatics data collection system is required

May develop/validate new methodologies or applications, process and evaluate data from samples for multi-site studies, evaluate data including study samples and quality control samples

Participate in routine equipment maintenance and instrument and/or assay troubleshooting, provide data collation, summarization, QC evaluation, and archiving as required

Contribute to biomarker assay validation, including planning, data collection, interpretation, and document authorship to support GLP and non-GLP multispecies safety studies and human clinical trials

Assure that laboratory activities meet quality standards such as Pfizer policies, SOPs, Environmental Health and Safety and departmental guidelines

BASIC QUALIFICATIONS

B.S. /B.A. in Medical Technology/Clinical Laboratory Science or related science related field with 2 years of experience within a Clinical Pathology laboratory in a hospital or diagnostic company, pharmaceutical company, or CRO; with knowledge of Good Laboratory Practices, data collection laboratory informatics systems, and data processing applications

Ability to handle multiple projects simultaneously, maintaining a high quality of Clinical Pathology data and timely delivery of results

Well organized, self-motivated, detail oriented, and has the ability to work and effectively communicate within a team environment

Excellent oral and written communication skills and ability to multitask. Highly motivated and enthusiastic scientist with proven record of independent analytical thinking and collaboration, ability to relish change, energize others and is passionate about work

Experience with laboratory information system and laboratory based workflows.

Problem-solving and critical thinking skills

PREFERRED QUALIFICATIONS

ASCP certified is preferred, but a candidate with strong biology skills and a willingness to learn clinical pathology assays will be considered.

Thorough understanding of the processes associated with pre-clinical and clinical study coordination and data management

Sunshine ActPfizer 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 provider's 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 EligibilityPfizer 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.Other Job Details:

Last Date to Apply for Job: September 2, 2019

Eligible for Employee Referral Bonus

#LI-PFEN (Other) (United States of America)Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.

Vacancy caducado!

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