GlaxoSmithKline (Israel) Ltd Posted August 31, 2026

PV Associate

Petach Tikvah, Israel Full time
Pharmacovigilance Associate
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GlaxoSmithKline (Israel) Ltd is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

GSK remains committed to achieving bold commercial ambitions for the future. By 2031, we aim to deliver £40 billion in annual sales, leveraging our existing strong performance momentum to significantly increase our positive impact on the health of billions of patients globally. Our Ahead Together strategy is centred on early intervention to prevent and alter the course of disease, thereby protecting people and supporting healthcare systems.

Our diverse portfolio consists of vaccines, specialty medicines, and general medicines.

Through continuous innovation and a dedicated focus on scientific and technical excellence, we strive to develop and launch new, groundbreaking treatments that address critical health challenges.

Position Summary

You will support the pharmacovigilance (PV) team in Israel by ensuring safety data and related systems are accurate and compliant. You will work closely with global and local colleagues, vendors and partners to process safety information, maintain PV records, and support reporting activities. We value accuracy, clear communication and a collaborative mindset. This role offers growth, meaningful impact on patient safety, and alignment with GSK’s mission of uniting science, technology and talent to get ahead of disease together.

Responsibilities

This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:

- Review, extract and accurately monitor adverse event (AE) data from spontaneous and solicited sources in the safety databases according to procedures.

- Perform quality checks, reconciliations and basic case triage to ensure data completeness and timeliness.

- Maintain and update pharmacovigilance agreements, safety documentation and document repositories.

- Run database listings and reports; support metric collection and basic trend checks.

- Liaise with local operating companies, vendors and internal teams to gather information and resolve data queries.

- Provide administrative and system support for PV processes, including mailbox triage and document archiving.

Why You?

Basic Qualifications & Skills

We are seeking professionals with the following required skills and qualifications to help us achieve our goals:

- Pharmacist with Israeli license.

- 1–4 years’ experience in pharmacovigilance / drug safety.

- Strong attention to detail and experience with data entry, reconciliation or database work.

- Good IT skills, including Excel and experience with web-based applications or safety databases.

- Ability to communicate clearly in Hebrew and English, both written and verbal.

- Comfortable working in a matrixed team and responding to stakeholders in a timely way.

Preferred Qualifications & Skills

If you have the following characteristics, it would be a plus:

- Experience with ICSR (Individual Case Safety Report) processing.

- Knowledge of local regulatory reporting requirements and pharmacovigilance methodology.

- Prior experience with safety databases (e.g., Argus, Veeva or similar) or document management systems.

- Experience working with vendors or in quality and compliance activities.

- Demonstrated experience in process improvement or KPI analysis.

Working arrangements

This role is hybrid. You will be expected to work on-site in Israel regularly and have flexibility for remote working as agreed with your manager.

How to apply

If this role matches your skills and ambitions, we encourage you to apply. Tell us how your experience fits the responsibilities and qualifications. We look forward to hearing how you can contribute to patient safety and grow with our team.

Skills

Digital Fluency, Drug Safety Surveillance, Pharmacovigilance

Why GSK?

Uniting science, technology and talent to get ahead of disease together.

GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.

People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.

Should you require any specific adjustments to our process to assist you in demonstrating your strengths and capabilities contact us on isr-inclusion.recruitment@gsk.com .

Please note should your enquiry not relate to adjustments, we will not be able to support you through these channels.

GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.

Important notice to Employment businesses/ Agencies

GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.

Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK’s compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at https://openpaymentsdata.cms.gov/

Job details

Seniority
Associate
Function
Pharmacovigilance
Therapeutic area
Not listed
Location
Petach Tikvah, Israel
Employment type
Full time

How this role compares

Computed from every other active Pharmacovigilance role in our database, not just this employer's listings.

We currently track 33 comparable Associate Pharmacovigilance roles across 18 biopharma companies.

33Comparable roles tracked
30Currently active
18Companies hiring similar roles
13Countries represented

Salary context

3 of 33 peers report a salary range (USD, annualized)

Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.

This roleSubject Not listed on this posting
Lowest disclosed · Manager, Pharmacovigilance Case Processing (Boston, MA, US) · Servier $131,000/yr – $150,000/yr
Peer group range $140,500 – $190,050 (median $152,000)

Where these roles are based

Top locations among the 33 comparable roles

United States8
India6
Poland4
France3
China2
Japan2

+ 7 more countries

Seniority mix

33 of 33 peers have a known seniority level

Manager30
Associate2
Intern/Fellow/Postdoc1

Therapeutic area mix

0 of 33 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

No peers with a known therapeutic area yet.

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

45%similar
BMS Services Sp. z o.o. Warsaw, Poland Associate
Same function Same seniority
45%similar
Boehringer Ingelheim Sydney, Australia Associate
Same function Same seniority
35%similar
Mylan AB Solna, Sweden Manager
Same function Adjacent seniority
35%similar
BMS Services Sp. z o.o. Warsaw, Poland Manager
Same function Adjacent seniority
35%similar
Amgen Inc. Remote, United States Manager
Same function Adjacent seniority
35%similar
Amgen Inc. Remote, United States Manager
Same function Adjacent seniority

Notify me about similar jobs

Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.

How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

45%
Pharmacovigilance Associate II
BMS Services Sp. z o.o. · Warsaw, Poland · Associate
Function Therapeutic area Seniority Country
35%
Senior Manager, Patient Safety Scientist
BMS Services Sp. z o.o. · Warsaw, Poland · Manager
Function Therapeutic area Adjacent seniority Country
35%
Pharmacovigilance Operations Senior Manager
Amgen Technology Pvt Ltd. · Hyderabad, India · Manager
Function Therapeutic area Adjacent seniority Country
35%
Intern - Patient Safety
Roche · Dhaka, Bangladesh · Intern/Fellow/Postdoc
Function Therapeutic area Adjacent seniority Country
Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.