Manager - Global Pharmacovigilance

Pharming Healthcare, Inc.; New Jersey; Hybrid; USD 105,000 - 135,000; Full time

Benefits offered by this job

Flexible hybrid schedule

Annual bonus

Long-term incentive

Job summary

Pharming Healthcare, Inc. is seeking a Pharmacovigilance Specialist to oversee safety case processing, signal detection, and risk assessment for Pharming products in development and post-authorization.

This hybrid role requires at least two days on-site at our Warren, NJ office, with the flexibility to collaborate across global PV activities and regulatory inquiries. You will maintain PV procedures, ensure regulatory timelines, and support data output for stakeholders while adhering to GCP/ICH

Qualifications

• BS degree in life sciences, pharmacy, or nursing; Masters/PharmD preferred.
• At least three years of pharmacovigilance and drug safety experience.
• Strong knowledge of PV and case processing.
• Familiarity with ARGUS safety databases.

Responsibilities

• Collect reported adverse events (SAEs) for Pharming products in development and post-authorization.
• Check completeness and consistency of reported information.
• Perform case assessment including seriousness and reportability.
• Enter data in PV databases and edit narratives as needed.
• Prepare follow-up queries and obtain missing information from reporters.

Skills

Pharmacovigilance

Drug safety evaluation

GCP/ICH guidelines

Regulatory compliance

Education

BS in life sciences, pharmacy or nursing

Masters or PharmD preferred

Tools

ARGUS

Job description

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.

This is a hybrid position requiring at least two days a week onsite at our office in Warren, NJ.

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

Who we are

We’re built on a simple belief: people living with rare diseases deserve more. Pharming is a global biotechnology company taking on some of the toughest rare disease challenges. We develop and commercialize innovative therapies for rare and ultra-rare immunological and genetic diseases with significant unmet need, where our scientific and commercial expertise, long-term commitment, and real partnership can help advance care.

We put patients at the heart of our work. Their insights, along with those of caregivers, clinicians, scientists, and parters, shape our strategy, guide our decisions, and help turn science into meaningful progress. We keep it simple, act with urgency, and get it done – expanding access to approved therapies, advancing high-value pipeline programs, and building a leading global rare disease company.

Our vision is simple: a world where people living with rare diseases don’t wait for progress or care. Together with the communities who inspire us, we’re opening new possibilities – proving that breakthroughs aren’t just discovered. They’re created together.

Ready to make a difference? Join us.

What it’s like to work here

At Pharming, every role helps move rare disease therapies closer to the people who need them. We make it happen together, across teams, disciplines, and borders, because breakthroughs don’t happen in silos. Rare diseases are complex, and meaningful progress takes people who ask better questions, challenge each other, and turn insight into action. Here, you won’t work on the sidelines. Pharming is a place for builders, problem-solvers, and bold thinkers who move with urgency, take ownership, and stay focused on what matters most: improving the lives of people living with rare diseases. Advancing rare disease care isn’t the work of one team or one leader. It’s all of us, building what’s next together.

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.

• 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
• Health and wellness program
• Choice of company provided mobile phone or cell phone stipend