Match score not available

Quality Specialist II - 100% remote - Pharmacovigilance Compliance

Remote: 
Full Remote
Contract: 
Salary: 
71 - 92K yearly
Experience: 
Mid-level (2-5 years)
Work from: 
New Jersey (USA), United States

Offer summary

Qualifications:

Bachelor's or Master's degree in life science, 4-5 years of relevant experience in Pharmacovigilance, Strong analytical skills and quality focus, Knowledge of Pharmacovigilance principles and regulations, Experience with investigation or deviation management.

Key responsabilities:

  • Review individual case safety report compliance outputs
  • Assist in developing compliance monitoring processes
  • Participate in special projects for data quality assurance
On-Board Companies logo
On-Board Companies Large https://www.onboardcompanies.com/
1001 - 5000 Employees
See more On-Board Companies offers

Job description

On-Board Scientific is hiring a Quality Specialist II (Pharmacovigilance Compliance) – 100% remote
For immediate consideration please send your resume to resumes@onboardusa.com
Subject Line: Position Title and State you are Located
About Us:
On-Board Services, Incorporated is an on-site contract service provider for a local manufacturing entity providing full-time positions to our employees. We offer benefits as well as 401k.
 
Position Details:
Job Title: Quality Specialist II – Pharmacovigilance Compliance
Position Type:  1 year contract with additional opportunity contingent upon performance and continued business need.
Job Location:
Shift: 1st shift
Compensation: $37.00 per hour
 
Quality Specialist II – 100% remote – Our client is Organon
Pay Rate: $48 per hour
Please note that this will start off as a 3 month contract assignment with the strong possibility of extension.
 
Responsibilities:
Under the direction and oversight of the PV Quality and Compliance Associate Director, this role will:
  • Perform reviews of individual case safety report compliance monitoring outputs to ensure high quality and compliant reporting in accordance with PV regulations and business partner agreements.
  • Assist with the development and implementation of processes used to monitor the compliance of individual case safety reports
  • Participate in compliance monitoring special projects as needed to ensure data quality .
 
Qualifications:
  • Bachelor's degree/Master's degree in life science with minimum 4-5 years of relevant experience within investigation, deviation in the Pharmacovigilance( PV) space.
  • Strong analytical skills and quality focus
  • Knowledge of Pharmacovigilance principles, systems, and requirements in addition to Pharmacovigilance regulations
  • Experience with Pharmacovigilance investigations or deviation management
 Software expertise:
  • Office 365 applications
  • Safety database(ARGUS is preferrable)
  • Will consider someone with similar software experience to ARGUS.
 Note:
  • 3 months assignment with possibility of extension.
  • 100% remote role.
  • Should have their own laptop or desktop to perform the work.
 Apply Today!
www.onboardusa.com
 
On-Board was founded in 1976 by Robert L. Wilson to provide Engineering and Design services to the chemical manufacturing industry. Today, On-Board is a thriving privately held family of companies with services including: Consulting, Professional Engineering, Industrial Maintenance and Facility Management, Contracted Manufacturing and Production Services, as well as Temporary Staffing and Recruiting throughout North America.

The On-Board Family of Companies conducts operations through its Corporate Headquarters located in East Windsor, NJ along with Regional Offices in New Castle, DE and Wake Forest, NC.  On-Board’s Mission is to provide “Flexible Service by applying the talents of our people, work processes and technology to meet our clients’ expectations in a Safe, Responsible and Dependable manner.”

On-Board Companies provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, religion, sex, national origin, age, disability or genetics.
 
JD# 24-02378
Tag: INDOJ

Required profile

Experience

Level of experience: Mid-level (2-5 years)
Spoken language(s):
English
Check out the description to know which languages are mandatory.

Other Skills

  • Analytical Skills

Compliance Officer Related jobs