Pfizer

Sr. Associate Central Monitor, Risk Based Monitoring, DMM

Employer
Pfizer
Location
Groton, Connecticut
Salary
Competitive
Posted
July 18 2021
Ref
4818452
Position Type
Full Time
Organization Type
Pharma
As part of the Data Monitoring and Management group, an integral delivery unit within the Global Biometrics and Data Management (GBDM) organization, the Sr. Associate Central Monitor is a highly technical team member responsible for ensuring the completeness, quality and integrity of the subject data in the clinical trial database under Risk Based Monitoring (RBM) model. Activities typically include developing the Risk-Based Monitoring system (i.e. CluePoints) for applicable studies, ensuring key risk indicators (KRIs) and data quality assessment (DQA) properly defined and set up in the system to support the study, processing and reviewing study data in the system for the signal and action management,and follow up for the issue resolution.

It is your dedication and focus that will help make Pfizer ready to achieve new milestones and help patients across the globe.

How You Will Achieve It

General
  • Implement global strategies, initiatives, processes, and standards to ensure consistent, efficient, and quality processes to meet quality, timelines and deliverables.
  • Provide technical expertise to set up and test study level Risk-based Monitoring system.
  • Review study level system outputs to process for the signal and action management.
  • Plan and execute communication plans & methods to ensure customer satisfaction and enable improvements to be implemented during the course of a study.
  • Able to resolve conflicts, influence and communicate cross-functionally with key stakeholders and customers.


System setup Functions:
  • Review protocols to ensure the set-up, review and reporting requirements can be met and are standardized.
  • Provide technical oversight, guidance and coordination for all the central monitor activities.
  • Set up and test RBM- Central Monitoring Analytics system at study level to ensure system quality.
  • Define key risk indicators (KRIs) in study system, and ensure consistency between the standard level and the study level.
  • Ensure RBM system alignment with the protocol and adherence to ICH GCP, SOPs, corporate standards and regulatory requirements.


Data review Functions:
  • Work with Study Team to define the issue resolution for the review of findings as signals and actions.
  • Develop, implement, and maintain Quality Control related documentation for RBM related activities to ensure data completeness and accuracy.
  • Perform central monitoring activities including review system outputs, propose suggestions for signal and action management, and follow up with study team for the action resolutions.
  • Work with Clinical Data Scientist (CDS) to ensure all signals and actions are properly mitigated and RBM systems properly released.
  • Ensure lessons learnt during the course of the study are documented and shared with other central monitors/ study teams to facilitate cross-study learning.


Qualifications

Must-Have

  • Bachelor's Degree in a scientific or business related discipline.
  • 3+ years' experience in data management/programming or data mining.
  • Demonstrated knowledge of clinical development including knowledge and understanding of the principles of GCP.
  • Understanding of clinical trials.
  • Awareness of relevant data standards, e.g. CDISC, CDASH, SDTM.
  • Experience with or ability to learn programming in a clinical trial environment, e.g. YAML script, SAS code, SQL query, R, Python, to extract and analyze operational and clinical trial data from various information systems.
  • Ability to critically analyze, interpret, and summarize statistical output from risk-based quality management software, e.g. CluePoints
  • Ability to manage tasks, time and priorities.
  • Demonstrated effective verbal and written communication skills, including the ability to communicate in a remote team environment and adapt communications to audience.


Nice-to-Have

  • Master's degree.
  • Relevant pharmaceutical industry experience.
  • Experience with or ability to learn data visualization techniques, e.g. Spotfire, JReview, Tableau.
  • Proficient experience using commercial clinical data management systems and/or EDC products.


Other Job Details:
  • Last Date to Apply for Job: July 21st
  • Eligible for Relocation Package: NO
  • Eligible for Employee Referral Bonus: YES
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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 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 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.

Medical

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