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Weekend Pharmacovigilance Jobs (NOW HIRING)

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Weekend Pharmacovigilance information

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$12

$49

$85

How much do weekend pharmacovigilance jobs pay per hour?

As of Jul 20, 2026, the average hourly pay for weekend 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.

Is pharmacovigilance a stressful job?

Pharmacovigilance jobs can be stressful due to the responsibility of monitoring drug safety and ensuring regulatory compliance, often involving tight deadlines and detailed data analysis. However, the level of stress varies depending on the workload, company culture, and individual experience, with some roles offering a more routine environment and others requiring quick decision-making. Proper training and organizational support can help manage stress levels in this field.

Will AI replace pharmacovigilance jobs?

AI is increasingly used in pharmacovigilance to assist with data analysis, signal detection, and case processing, but it is unlikely to fully replace pharmacovigilance professionals. Human expertise remains essential for interpreting complex safety data, making clinical judgments, and ensuring regulatory compliance. Pharmacovigilance jobs will evolve to incorporate AI tools, emphasizing skills in data analysis and regulatory knowledge.

How to break into pharmacovigilance?

Breaking into pharmacovigilance as a professional typically requires a background in pharmacy, medicine, or life sciences, along with knowledge of drug safety regulations and adverse event reporting systems. Gaining relevant certifications, such as the Drug Safety Certification (DSC), and developing skills in data analysis and medical writing can improve job prospects. Entry-level roles often require strong attention to detail and familiarity with regulatory guidelines like ICH E2E and FDA requirements.

What is the difference between Weekend Pharmacovigilance vs Pharmacovigilance Associate?

AspectWeekend PharmacovigilancePharmacovigilance Associate
CertificationsTypically requires a degree in pharmacy, life sciences, or related field; certifications like PV training are commonSame as Weekend Pharmacovigilance, often requiring similar educational background and certifications
Work EnvironmentPart-time, weekend shifts, often in pharmaceutical or biotech companiesFull-time or part-time, in clinical research organizations or pharmaceutical companies
Industry UsageUsed in companies needing weekend safety monitoring coverageCommon entry-level role in pharmacovigilance teams

Weekend Pharmacovigilance and Pharmacovigilance Associate roles share similar educational requirements and industry settings. The main difference lies in the work schedule, with Weekend Pharmacovigilance focusing on weekend shifts, while Pharmacovigilance Associates typically work full-time during weekdays. Both roles are essential for ensuring drug safety and require comparable qualifications.

What is the highest paid job in pharmacovigilance?

The highest paid roles in pharmacovigilance are typically senior positions such as Pharmacovigilance Directors or Global Safety Heads, who oversee drug safety strategies and compliance. These roles often require extensive experience, leadership skills, and knowledge of regulatory requirements, and they can earn salaries exceeding $150,000 annually depending on the company and location.

What are Weekend Pharmacovigilance jobs?

Weekend Pharmacovigilance jobs involve monitoring, assessing, and reporting on the safety of pharmaceutical products during weekends. Professionals in these roles review adverse event reports, ensure compliance with regulatory requirements, and may respond to urgent safety issues outside of regular business hours. These positions are crucial for maintaining continuous drug safety surveillance and supporting healthcare providers and patients at all times, including weekends.

What are the key skills and qualifications needed to thrive as a Weekend Pharmacovigilance professional, and why are they important?

To thrive as a Weekend Pharmacovigilance professional, you need a solid background in pharmacy, life sciences, or healthcare, often with a relevant degree and experience in drug safety or regulatory affairs. Familiarity with pharmacovigilance databases (such as Argus or ARISg), adverse event reporting systems, and knowledge of regulatory guidelines like ICH and FDA are typically required. Strong attention to detail, effective communication, and time management are important soft skills for handling urgent reports and collaborating remotely. These skills ensure timely and accurate monitoring of drug safety, compliance with regulations, and protection of patient well-being, even outside standard business hours.

What are the typical responsibilities and workflow for a Weekend Pharmacovigilance professional?

Weekend Pharmacovigilance professionals are primarily responsible for monitoring, assessing, and reporting adverse drug reactions and safety issues that arise during their shifts. Their workflow often involves triaging urgent safety cases, entering and validating case data, and collaborating with other team members to ensure timely regulatory submissions. Since much of the work occurs outside standard hours, strong communication with weekday teams is essential for seamless case handover and continuity. Additionally, they may participate in safety surveillance meetings or support ongoing investigations, making adaptability and attention to detail crucial in this role.
More about Weekend Pharmacovigilance jobs
What cities are hiring for Weekend Pharmacovigilance jobs? Cities with the most Weekend Pharmacovigilance job openings:
What are the most commonly searched types of Pharmacovigilance jobs? The most popular types of Pharmacovigilance jobs are:
What states have the most Weekend Pharmacovigilance jobs? States with the most job openings for Weekend Pharmacovigilance jobs include:
Infographic showing various Weekend Pharmacovigilance job openings in the United States as of July 2026, with employment types broken down into 13% Locum Tenens, 48% As Needed, 9% Full Time, 13% Temporary, 16% Nights, and 1% Summer. Highlights an 80% Physical, 2% Hybrid, and 18% Remote job distribution, with an average salary of $102,217 per year, or $49.1 per hour.
Pharmacovigilance Specialist

Pharmacovigilance Specialist

Rishabh RPO

Los Angeles, CA • On-site

Contractor

Re-posted 10 days ago


Job description

Title: Pharmacovigilance Specialist

Location: Los Angeles, CA 90032

Duration- 4 months (Possible extension for long term)

FAQ
This position is for Adverse event monitoring. This person will deal with marketed products and side effects, follow up with reporters (patients, Doctors, etc.), and triage case reports. Looking for someone with a background in Pharmacovigilance who can follow international regulatory guidelines.
Preference is for the ARGUS database. PSUR exp would be nice.

The interview will consist of a phone screen with the local manager and a second phone screen with management in Barcelona. The team is based in LA, but it is a global team and will need someone who can be flexible in scheduling meetings across multiple time zones.

Summary:

  • Provides operational support for global pharmacovigilance activities of client's marketed products.
  • Ensures pharmacovigilance deliverables are of the highest quality and meet global regulatory reporting timelines.
  • Responsible for data review, compilation, and analysis, including management of the integrated safety database.
Primary responsibilities for the role:
  • Management of Adverse Events including activities such as processing adverse event case reports and conducts follow-up .
  • Notifies regulatory agencies and business partners accordingly; responds to requests from regulatory agencies
  • Reviews scientific literature and bibliographic sources; draft and manage periodic safety update reports. .
  • Evaluates safety profiles; draft and manage signal detection reports; ensures document filing and archiving. .
  • Participation in the processes involving the collection, processing, review and distribution of adverse event information regarding development and marketed client's pharmaceutical products. .
  • Contributes to ensure compliance of pharmacovigilance activities including activities such as conduct case reconciliation with concerned departments, affiliates, distributors or business partners .
  • Take part in self-inspection visits, audits, inspections and in CAPAs management, create or update pharmacovigilance procedures and working practices .
  • Provide training to concerned persons based on the training plan and managing training documentation; archive documents according to prevailing standards .
  • Support in the procedures of global pharmacovigilance operations such as Standard Operation Procedures (SOPs), internal business practices or working instructions. .
  • Serves in an advisory capacity including activities such as product monographs review, draft responses to pharmacovigilance requests from regulatory agencies; participates in the drafting and implementation of pharmacovigilance contracts and agreements. be sure to see notes before submitting candidates.

Questions to be answered

  1. List specific areas of expertise in Pharmacovigilance you have focused on.
  2. What safety database(s) have you used, and what types of cases have you processed?

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About Rishabh BPO Services

Sourced by ZipRecruiter

Rishabh BPO is the right choice for companies looking to outsource their business processes to lower their costs, eventually resulting in a transformation of the way the company works. The general benefits of BPO are well known in the industry today. Long term approach of engaging with the customers: This means that Rishabh BPO will focus on getting value for their customers by investing their own resources in the short-term so that the clients experience the value of working with Rishabh BPO over the entire engagement.

Industry

Business management consulting

Company size

51 - 200 Employees

Headquarters location

San Jose, CA, US

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