Current jobs related to Pharmacovigilance Specialist - Jersey City, New Jersey - eTeam


  • Jersey City, New Jersey, United States YD Talent Solutions Full time

    Job DescriptionAbout our client:Our client is a leading provider of pharmacovigilance solutions, leveraging advanced technologies to develop agile, flexible, and scalable systems that address challenges across Medical Affairs, Regulatory, and Safety functions.Their solutions enable pharmaceutical companies to free up responsible personnel, execute their...


  • Jersey City, New Jersey, United States eTeam Full time

    Job Title: Quality Assurance SpecialistWe are seeking a highly skilled Quality Assurance Specialist to join our team at eTeam. As a Quality Assurance Specialist, you will play a critical role in ensuring the quality and compliance of our Pharmacovigilance (PV) operations.Key Responsibilities:Perform reviews of individual case safety report compliance...


  • Jersey City, New Jersey, United States eTeam Full time

    Job Title: Quality SpecialistJoin eTeam as a Quality Specialist and contribute to the success of our organization by ensuring the highest quality and compliance in our Pharmacovigilance operations.About the Role:Under the direction of the PV Quality and Compliance Associate Director, this role will be responsible for performing reviews of individual case...


  • Jersey City, New Jersey, United States eTeam Full time

    Quality Assurance SpecialistAs a Quality Assurance Specialist at eTeam, you will play a crucial role in ensuring the high quality and compliance of individual case safety report monitoring outputs. Under the direction of the PV Quality and Compliance Associate Director, you will perform reviews of compliance monitoring outputs, assist in the development and...


  • Jersey City, New Jersey, United States eTeam Full time

    Job Title: Quality SpecialistAt eTeam, we're seeking a highly skilled Quality Specialist to join our team. As a Quality Specialist, you will be responsible for ensuring high-quality reporting in accordance with PV regulations and business partner agreements.Key Responsibilities:Perform reviews of individual case safety report compliance monitoring outputs to...


  • Jersey City, New Jersey, United States Mitsubishi Tanabe Pharma Full time

    Job SummaryMitsubishi Tanabe Pharma America is seeking a highly skilled Manager, Drug Safety to support signal detection activities and medical analyses to evaluate and characterize safety topics for products. The successful candidate will work closely with the Drug Safety Global Safety Team (GST) Chair (Medical Director) to perform signal management process...


  • Jersey City, New Jersey, United States The Fountain Group Full time

    Job Title: Paralegal - II (Associate)Job Description:Key Responsibilities:Review contract intake forms and collaborate with procurement owners to obtain any missing information.Determine contracting requirements based on assigned requests.Ability to review historical contract information to assess current contracting requirements.Draft necessary contract...


  • Oregon City, Oregon, United States Innomar Strategies Full time

    Job SummaryWe are seeking a highly skilled and detail-oriented Associate Bilingual Drug Safety Specialist to join our team at Innomar Strategies. As a key member of our Pharmacovigilance department, you will play a critical role in ensuring the safety and efficacy of our products.Key Responsibilities:Receive, scan, and document all pertinent clinical...


  • Foster City, United States LanceSoft, Inc. Full time

    Title: Vendor Qualification Associate.Location: Foster City, CA or Remote.Duration: 12+Months Contract.Pay Range: $35.00/ Hr to $40.00/ Hr on W2Description:The Vendor Qualification Associate is expected to complete tasks and projects under minimal supervision and has the ability to manage competing priorities effectively and proficiently. Demonstrates a...


  • Foster City, CA, United States LanceSoft, Inc. Full time

    Title: Vendor Qualification Associate.Location: Foster City, CA or Remote.Duration: 12+Months Contract.Pay Range: $35.00/ Hr to $40.00/ Hr on W2Description:The Vendor Qualification Associate is expected to complete tasks and projects under minimal supervision and has the ability to manage competing priorities effectively and proficiently. Demonstrates a...

  • Project Specialist

    1 week ago


    Foster City, United States ATR International Full time

    12 month contract ($33-$40/hr)Hybrid scheduleWe are seeking a Vendor Qualification Associate I for a very important client who will report to the Senior Manager of Vendor Outsourcing. The candidate will be responsible for ensuring high quality of data and services across all vendors supporting The Client’s global R&D portfolio – Ph I-IV clinical...


  • Foster City, United States SPECTRAFORCE Full time

    Title : Vendor Qualification Associate ILocation : Foster City, CA or Santa Monica, CA, Seattle (Remote)Duration :12 MonthsDescription:Vendor Qualification Associate I, who will report to the Senior Manager of Vendor Outsourcing. The candidate will be responsible for ensuring high quality of data and services across all vendors supporting global R&D...

Pharmacovigilance Specialist

2 months ago


Jersey City, New Jersey, United States eTeam Full time
Job Title: Pharmacovigilance Specialist

Location: Remote

Duration: 3 Months extendable contract

Pay: $45.86/hr

About the Role:

This role will report to the PV Quality and Compliance Associate Director and will be responsible for ensuring high-quality and compliant reporting in accordance with PV regulations and business partner agreements.

Key Responsibilities:

  • Perform reviews of individual case safety report compliance monitoring outputs to ensure high-quality and compliant reporting.
  • 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.

Requirements:

  • 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 in Office 365 applications, Safety database (ARGUS is preferable), and similar software experience to ARGUS.

What We Offer:

  • 3 months assignment with possibility of extension.
  • 100% remote role.
  • Opportunity to work with a reputable company like eTeam.