Manager - Global Pharmacovigilance

Pharming Group N.V.

• $105K — $135K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • BS in life sciences, pharmacy, or nursing; Master's or PharmD preferred
  • Minimum of 3 years in pharmacovigilance and drug safety
  • Strong expertise in case processing and drug safety evaluation
  • Proficient in using pharmacovigilance databases, especially ARGUS
  • Thorough understanding of pharmacovigilance practices and regulations
  • Knowledgeable in GCP/ICH guidelines
  • Alignment with Pharming's mission and values

Responsibilities

  • Collect and collate (S)AE reports for products in development and post-authorization.
  • Ensure completeness and consistency of reported safety data.
  • Assess cases for seriousness and reportability.
  • Enter data into the Pharmacovigilance database and edit narratives.
  • Prepare follow-up queries and communicate with reporters for additional information.
  • Submit individual case safety reports to authorities like the FDA and EMA within legal timelines.
  • Develop database queries and visual data outputs for stakeholders.

Benefits

  • Flexible hybrid work schedule
  • Competitive compensation package with annual target bonus
  • Long-term incentive program
  • 401(k) plan with company match
  • Paid Time Off (PTO)
  • 13 Company Holidays per year
  • Comprehensive medical, dental, and vision plans
  • Flexible spending accounts
  • Company-provided life insurance and disability plans
  • Optional insurance plans for accidents, critical illness, etc.
  • Tuition reimbursement program
  • Health and wellness program
  • Choice of company-provided mobile phone or stipend
Full Job Description
Summary

This position provides safety evaluation of Pharming product(s), including case processing, signal detection and workups. Our goal for this position is to proactively manage potential safety issues, oversee the processing of (S)AE reporting, perform data retrieval and respond to regulatory agency safety enquiries. Successful execution will involve in depth knowledge of current drug safety regulations and a sufficient level of case management expertise.

What you'd do

  • Collecting and collating reported (S)AEs associated with the use of Pharming's product(s) both in development and post-authorization.
  • Checking reported information on completeness and consistency of data.
  • Performing case assessment including determining seriousness, reportability etc.
  • Entering all relevant data in the Pharmacovigilance database including editing narratives.
  • Preparing follow-up queries and communicating with the reporters to obtain follow-up information for the (S)AEs received.
  • Responsible for expedited submission of individual case safety reports to competent authorities, i.e., FDA, EMA, Ethics Committees, partners and other parties as applicable within timelines specified per applicable legal requirement (e.g., 7/15 day reporting timeline).
  • Developing data output: database queries and data visualization in support of internal stakeholder requests (aggregate reports, signaling outputs, reconciliation, etc).
  • Answering and/or supporting/contributing to the answering of questions from competent authorities.
  • Performing reconciliation of safety information arising from clinical trials with data management.
  • Alerting company personnel of any possible adverse changes to the risk-benefit profile of company products and providing relevant information as required to make an assessment.
  • Maintaining a current awareness of legislation and practices relating to PV and ensuring the company complies with changing global requirements through updating procedures, practices and database configuration as appropriate.
  • Designing and implementing procedures to ensure the smooth running of the Pharmacovigilance Department.
  • Ensuring compliance of partner/distributors with local pharmacovigilance agreements by supporting routine and for cause GvP audits.
  • Overseeing the database set-up of all new studies including the preparation of study specific SAE processing documents (e.g., Safety Reporting Plan).
  • Assisting Business Development in all safety related issues required for the preparation of proposals/contracts for partners/distributors.
  • Performing other related duties as assigned or requested by the PV Senior Manager and the VP, GPV.
  • Providing out of office support for other PV staff, as required.
  • Other duties as assigned.


What you'd need

  • BS Degree in relatable subjects i.e. life sciences, pharmacy or nursing; Masters or PharmD degree preferred
  • At least three years of industry experience in pharmacovigilance and drug safety
  • Extensive knowledge of pharmacovigilance especially case processing and drug safety evaluation
  • Extensive knowledge of safety database (ARGUS strongly preferred)
  • In depth understanding of good pharmacovigilance practices and current drug safety regulations
  • Good knowledge of GCP/ICH guidelines.
  • Commitment and alignment to Pharming's mission and values


Salary range

Pharming takes into consideration a combination of candidate's work experience, training, and education, as well as the scope of the role, complexity, and external market and internal value when determining a salary level.

The base salary range for this job is from $105,000 to $135,000 per year.

Compensation & benefits

  • Flexible hybrid work schedule to promote a healthy work-life balance


  • Competitive compensation package including annual target bonus


  • Long-term incentive program


  • 401(k) plan with company match


  • Paid Time Off (PTO)


  • 13 Company Holidays per year


  • Excellent benefit plans including medical, dental, and vision


  • Flexible spending accounts


  • Company-provided life insurance, short-term disability, and long-term disability plans


  • Optional accident, hospital indemnity, critical illness, and pet insurance plans


  • Tuition reimbursement program


  • Health and wellness program


  • Choice of company provided mobile phone or cell phone stipend

Similar Jobs

More Jobs at Pharming Group N.V.

More Pharmaceuticals & Biotech Jobs

Find similar Manager - Global Pharmacovigilance jobs: