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Weekend Pharmacovigilance Jobs (NOW HIRING)

Med Communications

Pharmacovigilance Physician

Pharmacovigilance Reports To: Global Head of Pharmacovigilance and Drug Safety Employment Type: Contractor Join our Team Med Communications is seeking a Pharmacovigilance Physician (MD, DO, or ...

AA2IT

Pharmacovigilance

North Wales, PA · On-site

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 ...

Fladger Associates

Pharmacovigilance (PV)

Boston, MA · On-site

Excellent employment opportunity for a Pharmacovigilance (PV) in the Boston, MA area. * We are looking for a Pharmacovigilance Scientist (approximately 25 hours per week) who can support us in ...

VENESCO LLC

Pharmacovigilance Physician

Frederick, MD · On-site

Pharmacovigilance Physician Venesco is seeking a Pharmacovigilance Physician to provide medical oversight and clinical expertise for all safety surveillance and pharmacovigilance activities. The ...

Umoja Biopharma

Director, Pharmacovigilance

$204K - $305K/yr

The Director of Pharmacovigilance (PV) will play a critical role in executing Umoja Biopharma's global safety strategy across clinical-stage programs. This individual will be responsible for day-to ...

ICON

Senior Pharmacovigilance Associate

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Senior Pharmacovigilance Associate ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a ...

YO AI Labs

Pharmacovigilance Expert - Remote

San Jose, CA · Remote

$70 - $80/hr

Pharmacovigilance Expert Job Type: Contractor Location: Remote Job Overview We are seeking experienced Pharmacovigilance Experts to contribute their drug safety expertise to an innovative healthcare ...

YO AI Labs

Pharmacovigilance Expert - Remote

Atlanta, GA · Remote

$70 - $80/hr

Pharmacovigilance Expert Job Type: Contractor Location: Remote Job Overview We are seeking experienced Pharmacovigilance Experts to contribute their drug safety expertise to an innovative healthcare ...

YO AI Labs

Pharmacovigilance Expert - Remote

Chicago, IL · Remote

$70 - $80/hr

Pharmacovigilance Expert Job Type: Contractor Location: Remote Job Overview We are seeking experienced Pharmacovigilance Experts to contribute their drug safety expertise to an innovative healthcare ...

YO AI Labs

Pharmacovigilance Expert - Remote

Seattle, WA · Remote

$70 - $80/hr

Pharmacovigilance Expert Job Type: Contractor Location: Remote Job Overview We are seeking experienced Pharmacovigilance Experts to contribute their drug safety expertise to an innovative healthcare ...

YO AI Labs

Pharmacovigilance Expert - Remote

Phoenix, AZ · Remote

$70 - $80/hr

Pharmacovigilance Expert Job Type: Contractor Location: Remote Job Overview We are seeking experienced Pharmacovigilance Experts to contribute their drug safety expertise to an innovative healthcare ...

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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 Aug 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.

What is a weekend pharmacovigilance?

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 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.

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 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.

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:

What job categories do people searching Weekend Pharmacovigilance jobs look for?

The top searched job categories for Weekend Pharmacovigilance jobs are:

Weekend Pharmacovigilance jobs near you
Infographic showing various Weekend Pharmacovigilance job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 68% Full Time, 26% Part Time, 4% Contract, and 1% Nights. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $102,217 per year, or $49.1 per hour.

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

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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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