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Aggregate In Pharmacovigilance Jobs (NOW HIRING)

AA2IT

Pharmacovigilance

North Wales, PA · On-site

... case and aggregate safety reporting in accordance with pharmacovigilance (PV) policy and ... regulations. * Assist in the management and maintenance of PV-controlled documents (e.g. Global ...

Jobgether

Proven professional experience in pharmacovigilance, with demonstrated involvement in activities such as ICSR processing and quality review, aggregate report writing or contribution, literature ...

ProPharma Group

The Senior Pharmacovigilance (PV) Scientist supports the activities in the Benefit Risk group by ... Well-rounded experience in literature screening activities and/or authoring and reviewing aggregate ...

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Aggregate In Pharmacovigilance information

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$12

$49

$85

How much do aggregate in pharmacovigilance jobs pay per hour?

As of Aug 19, 2026, the average hourly pay for aggregate in pharmacovigilance in the United States is $49.14, according to ZipRecruiter salary data. Most workers in this role earn between $38.46 and $55.53 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as an aggregate in pharmacovigilance?

To thrive in an Aggregate role in Pharmacovigilance, you need a solid background in life sciences or pharmacy, strong analytical abilities, and experience with safety data analysis and regulatory reporting. Familiarity with pharmacovigilance databases (such as Argus or ArisG), signal detection tools, and an understanding of global regulatory guidelines (e.g., ICH, EMA, FDA) are typically required. Excellent attention to detail, organizational skills, and effective communication are essential soft skills for interpreting complex data and collaborating across teams. These competencies are crucial for ensuring accurate safety reporting, regulatory compliance, and the protection of patient health.

What are some common challenges faced by professionals working in aggregate reporting within pharmacovigilance?

Professionals involved in aggregate reporting in pharmacovigilance often encounter challenges such as managing large volumes of data from multiple sources, ensuring compliance with evolving global regulatory requirements, and meeting strict submission deadlines. Coordinating with cross-functional teams—such as clinical, regulatory, and safety departments—is essential for gathering accurate information and maintaining data consistency. Attention to detail and strong organizational skills are crucial to ensure that periodic safety update reports (PSURs), periodic benefit-risk evaluation reports (PBRERs), and other aggregate reports are comprehensive and error-free.

What is the difference between Aggregate In Pharmacovigilance vs Pharmacovigilance Associate?

AspectAggregate In PharmacovigilancePharmacovigilance Associate
CredentialsTypically requires a degree in life sciences, pharmacy, or related field; certifications like PV training are commonSimilar educational background; often requires PV-specific training or certifications
Work EnvironmentFocuses on data analysis, signal detection, and reporting of safety data at a higher levelInvolves data entry, case processing, and supporting safety reports
Employer & Industry UsageUsed in pharmaceutical companies, CROs, and regulatory agencies for safety data analysisCommonly employed in similar settings for case management and data entry

In summary, Aggregate In Pharmacovigilance primarily handles data analysis and safety signal detection, requiring advanced skills in data interpretation. Pharmacovigilance Associates focus on case processing and data entry tasks. Both roles require relevant certifications and work within the same industry environment, but differ in scope and responsibilities.

What is aggregate reporting in pharmacovigilance?

In pharmacovigilance, aggregate reporting involves compiling and analyzing safety data from multiple individual adverse event reports over a specific period to identify safety signals and trends. Pharmacovigilance professionals use tools like safety databases and statistical methods to prepare periodic safety update reports (PSURs) and aggregate reports required by regulatory authorities.
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Aggregate In Pharmacovigilance jobs near you
Infographic showing various Aggregate In Pharmacovigilance job openings in the United States as of August 2026, with employment types broken down into 84% Full Time, 14% Part Time, 1% Contract, and 1% Nights. Highlights an 83% Physical, 2% Hybrid, and 15% Remote job distribution, with an average salary of $102,217 per year, or $49.1 per hour.

Pharmacovigilance

AA2IT

North Wales, PA • On-site

Other

Re-posted 12 days ago

Job description

Pharmacovigilance Safety Specialist

Education: Bachelor's degree or Master's degree or Advance level degree in a life science/healthcare/pharmaceutical related field.

Required: Candidate is required to have at least 2 years of pharmacovigilance safety experience or related areas such as Clinical Risk Management, Clinical or Regulatory preferred. Strong knowledge base of pharmacovigilance principles with close attention to detail and ability to be flexible in order to meet daily competing priorities of the business. Ability to independently contribute effectively to group projects, handle individual tasks, and take initiative when necessary. Veeva Vault experience preferred.

Software: MS office suite. Veeva Vault is preferred.

Personality: Detail Oriented. Able to work independently. Team Player. Excellent written and verbal communication skills.

Note: 1 year assignment. Hybrid assignment (2 days/week onsite). Work Location: Upper Gwynedd, PA.

Documentation and training role. Writing SOP's - we are responsible for maintaining Individual Case Safety Report (ICSR) and aggregate reporting. More focus is on the Individual Case Safety Report (ICSR). Familiarity with any Learning management system. Experience with My learning system is a plus. Need someone who can deliver and create trainings. Experience with safety database. Experience with VEEVA Vault is a plus.

Responsibilities:

We are looking for (2) Contractors to support PV Operations and Global Process Enablement in Documentation and Training and PV Quality and Compliance with responsibilities to include:

  • Documentation, training, and global standards team within Client in need of a supportive and highly motivated individual within their team that will assist in developing and maintaining documents outlining the processes to ensure high quality individual case and aggregate safety reporting in accordance with pharmacovigilance (PV) policy and regulations.
  • Assist in the management and maintenance of PV-controlled documents (e.g. Global Safety Database User Manual, Standard Operating Procedures, and training material).
  • Assist in the authoring, reviewing and implementation of new PV-controlled SOPs and supportive documents.
  • Assist in reviewing, creating, and delivering trainings.
  • Process incoming communications from internal and external sources and initiate appropriate course of action and/or response.
  • Perform quality review of expedited and periodic reports to ensure adherence to global case processing standards and regulatory requirements.
  • Monitor group mailboxes utilized for the centralization of process/subject specific inquiries.

Comments/Special Instructions: Documentation and training role. Writing SOP's-we are responsible for maintaining Individual Case Safety Report (ICSR) and aggregate reporting. More focus of Individual Case Safety Report (ICSR). Familiarity with LMS-My learning is a plus. Someone who can deliver and create trainings. Experience with safety database. Experience with VEEVA Vault is a plus.

If interested, kindly send updated copy of resume with following answers:

  • Which year you graduated your Bachelor's degree or Master's degree or Advance level degree and in which Discipline
  • How many years of exp in pharmacovigilance safety or related areas such as Clinical Risk Management, Clinical or Regulatory
  • How many years of exp in Writing SOP's-& maintaining Individual Case Safety Report (ICSR)and aggregate reporting.
  • How far you live from 351 North Sumneytown Pike, North Wales, PA and how will you commute daily
  • Giving Exclusive right to represent to our client for req ID: 35411

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