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Remote Pharmacovigilance Associate Jobs (NOW HIRING)

YO AI Labs

Biology Research Scientist - Remote

Miami, FL · Remote

$50 - $70/hr

Pharmacology * Binding & Functional Assays * Scientific Data Interpretation * Evidence-Based ... Currently active in a bench-based research, scientist, or associate scientist role. * Working ...

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How much do remote pharmacovigilance associate jobs pay per hour?

As of Sep 6, 2026, the average hourly pay for remote pharmacovigilance associate 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 remote pharmacovigilance associate?

A Remote Pharmacovigilance Associate is a pharmaceutical professional who monitors, evaluates, and reports on the safety of drugs and medical products, working from a remote location rather than an onsite office. Their main responsibilities include collecting and analyzing data on adverse drug reactions, ensuring compliance with regulatory requirements, and contributing to the overall safety profile of medications. They typically collaborate with clinical teams, regulatory authorities, and healthcare professionals to ensure that any potential risks associated with pharmaceutical products are identified, documented, and communicated promptly.

What are the key skills and qualifications needed to thrive as a remote pharmacovigilance associate, and why are they important?

To thrive as a Remote Pharmacovigilance Associate, you need a solid background in life sciences or pharmacy, attention to detail, and knowledge of drug safety regulations such as GVP and ICH guidelines. Familiarity with pharmacovigilance databases (like Argus Safety or ARISg), case processing systems, and relevant certifications such as a PV certification are commonly required. Strong written communication, critical thinking, and the ability to work independently are standout soft skills in this position. These skills ensure accurate safety data collection, regulatory compliance, and effective remote teamwork for patient safety.

What are some common challenges faced by remote pharmacovigilance associates, and how can they be managed effectively?

Remote Pharmacovigilance Associates often face challenges such as maintaining clear communication with cross-functional teams and ensuring timely reporting of adverse events. Working remotely can sometimes make it harder to access support or quickly clarify regulatory guidelines, so successful associates proactively leverage digital collaboration tools and maintain regular contact with supervisors and colleagues. Staying organized, adhering to standardized procedures, and participating in ongoing training sessions also help manage workload and ensure compliance with global safety regulations.
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Remote Pharmacovigilance Associate jobs near you
Infographic showing various Remote Pharmacovigilance Associate job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 70% Full Time, 27% Part Time, 1% Temporary, and 1% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $102,217 per year, or $49.1 per hour.

Biology Research Scientist - Remote

YO AI Labs

Boston, MA • Remote

$50 - $70/hr

Full-time

Posted 12 days ago

Job description

Biology Research Scientist

Job Type: Contractor
Location: Remote
Hours: 10–20 hours/week
Duration: 1–2 months minimum, with likely extension
Start: Immediate

Job Overview

We are seeking experienced Biology Research Scientists to support a project focused on validating protein target assignments against primary scientific sources and UniProt records.

You will review research papers and patents, identify target assignment errors, propose corrected UniProt accessions, and provide concise, evidence-based scientific reasoning.

Key Responsibilities
  • Review primary research papers and patents to verify protein target assignments.
  • Compare target assignments against UniProt and identify discrepancies.
  • Classify target assignment errors using a structured taxonomy.
  • Propose accurate UniProt accessions where assignments are incorrect.
  • Document clear, concise, evidence-grounded reasoning for each determination.
  • Apply expertise in pharmacology, biochemistry, molecular biology, or chemical biology to evaluate target relationships.
Required Skills
  • Protein Target Identification
  • UniProt
  • Primary Literature Review
  • Protein Biochemistry
  • Molecular Biology
  • Pharmacology
  • Binding & Functional Assays
  • Scientific Data Interpretation
  • Evidence-Based Reasoning
  • Technical Documentation
Qualifications
  • BA/BS + 5 years, MS + 2 years, or PhD with relevant industry/drug discovery experience.
  • Background in pharmacology, biochemistry, molecular biology, or chemical biology within biotech, pharma, or CRO environments.
  • Hands-on experience with assays such as SPR, TR-FRET, radioligand binding, kinase assays, or GPCR functional assays.
  • Experience interpreting IC50, Ki, and Kd data.
  • Currently active in a bench-based research, scientist, or associate scientist role.
  • Working knowledge of UniProt or related workflows such as SAR, HTS, target validation, biochemical profiling, or IND-enabling studies.
Nice to Have
  • Experience with ChEMBL, BindingDB, or PubChem.
  • Selectivity profiling or counterscreening experience.
  • Understanding of agonist/antagonist vs. activator/inhibitor distinctions.
Screening Questions
  1. What is your highest relevant degree and how many years of industry research experience do you have?
  2. What is your experience with protein target identification and UniProt?
  3. Which binding or functional assays have you performed hands-on?
  4. Do you have experience interpreting IC50, Ki, or Kd data?
  5. Have you worked with ChEMBL, BindingDB, or PubChem?
  6. Are you currently bench-active in a research or scientist role?
  7. Are you available for 10–20 hours per week with an immediate start?