Pharmacovigilance Pv Analytics And Reporting Specialist

  • Lawrenceville, New, United States
  • Full-time
  • Salary: Not Available
  • Posted on:
  • Expires on:

JOB TITLE:

Pharmacovigilance Pv Analytics And Reporting Specialist

JOB Type:

CTC

JOB SKILLS:

Not Provided

JOB Location:

Lawrenceville, New, United States

JOB DESCRIPTION

Pharmacovigilance (PV) Analytics and Reporting Specialist Pharma (Hybrid Lawrenceville, NJ)

We are seeking a Pharmacovigilance (PV) Analytics and Reporting Specialist for a global pharmaceutical company. You will be responsible for successful execution, and close-out of activities aligned with the overall vision, strategy, and objectives of the Global Biostatistics & Data Sciences Function. The PV Analytics and Reporting Specialist contributes to the ongoing development, implementation, and successful execution of the scientific, operational, and regulatory reporting efforts.

This is a 40-hour per-week, 12-month contract (extensions possible), 50% onsite role in Lawrenceville, NJ.

This is a W2 role as a Stage 4 Solutions employee. Health benefits and 401K are offered.

Responsibilities:

  • Build and continuously improve data analytics through supporting models that provide insights into efficiency, quality, stakeholder feedback, and key performance indicators to drive timely and informed decision making

  • Maintain and develop reporting databases and analytics applications in environments such as Excel, Tableau, Spotfire, Power BI, SAP Business Objects and/or other BMS environments

  • Liaison with validation team to create validation test script, validation plan, validation summary report and test scripts.

  • Contribute to qualitative and quantitative research projects through collaboration with data trends from cross-functional teams (Pharmacovigilance, Epidemiology, etc.)

  • Utilize data analysis tools to aggregate and analyze data to make actional recommendations and answer key business questions

  • Run and maintain reports regarding activities, outcomes, and be prepared to deliver presentations to management team on a regular and ad-hoc basis

  • Continually remain apprised of the constantly changing landscape of the healthcare industry and any impacts it may have to our Analytical programs and reporting mechanisms

  • Analyze key stakeholder complaints, address rapidly, and discuss with applicable functional leads to collaborate and propose impactful and realistic solutions

  • Define and provide metric reporting and data analysis for GBDS/WWPS initiatives including relevant insights to facilitate decision-making process

Requirements:

  • Bachelor's or Master's Degree with a Life Sciences, Information, or similar background

  • 5+ years Drug Safety/Pharmacovigilance experience

  • Advanced Tableau and SAP Business Objects (BO) skills with 5+ years of development experience

  • Databases (Oracle, Impala, etc.)

  • Programming languages (SQL, VBA, Python etc.)

  • Knowledge and application of commercial coding dictionaries (MedDRA, WHO Drug)

  • Knowledge of taxonomies, ontologies, and other knowledge management constructs

  • Knowledge of Validation processes and associated documentation.

Please feel free to forward this project opening to others who may be interested.

Stage 4 Solutions is an equal-opportunity employer. We celebrate diversity and are committed to providing employees with an inclusive environment that is free of discrimination and harassment. All employment decisions are based on the job requirements and candidates' qualifications, without regard to race, color, religion/belief, national origin, gender identity, age, disability, marital status, genetic information, or other applicable legally protected characteristics.

Compensation: $50/hr. - $57.65/hr.

Position Details

Posted:

Employment:

CTC

INDUSTRY:

-

Salary:

USD 82 per hour

REFERENCE NUMBER:

SNPR-474650

CITY:

Lawrenceville

JOB ORIGIN:

SNPR