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Remote Drug Safety Associate Jobs in Woonsocket, RI

NTT DATA Services

TEMP BPO Associate

Lincoln, RI · On-site +1

$14.75 - $19.50/hr

... drug benefit exceptions, appeals) via phone and fax from members and prescribers. Accurately set up ... While many positions offer remote or hybrid work options, these arrangements are subject to change ...

Danaher

Senior Engineer, Process Validation

Boston, MA · On-site +1

$100K - $130K/yr

... remote. In this role, you will have the opportunity to: * Design, execute, and summarize ... Mentor junior validation associates in Process Validation, cGMP regulations, and principles of ...

Danaher

Senior Engineer, Process Validation

Boston, MA · On-site +1

$100K - $130K/yr

... remote. In this role, you will have the opportunity to: * Design, execute, and summarize ... Mentor junior validation associates in Process Validation, cGMP regulations, and principles of ...

UNFI

Retail Pricing Specialist

Providence, RI · On-site +1

... safety rules, operating and maintenance instructions, and procedure manuals. Ability to write ... Remote associates are welcome to work from the office but are not required to do so. While remote ...

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Remote Drug Safety Associate information

See Woonsocket, RI salary details

$11

$47

$82

How much do remote drug safety associate jobs pay per hour?

As of Sep 7, 2026, the average hourly pay for remote drug safety associate in Woonsocket, RI is $47.09, according to ZipRecruiter salary data. Most workers in this role earn between $36.88 and $53.22 per hour, depending on experience, location, and employer.

What is a remote drug safety associate?

A Remote Drug Safety Associate is responsible for monitoring, assessing, and reporting adverse drug reactions (ADRs) to ensure medication safety and regulatory compliance. They review patient safety data, prepare safety reports, and liaise with healthcare professionals and regulatory agencies. Working remotely, they use specialized databases and communication tools to track and analyze drug safety information. Their role is crucial in ensuring that pharmaceuticals remain safe for consumers while complying with industry regulations.

What does a remote drug safety associate do?

A typical workday for a Remote Drug Safety Associate involves reviewing and processing adverse event reports, entering data into safety databases, and preparing regulatory submissions. You may also participate in teleconferences with cross-functional global teams, respond to queries from regulatory bodies, and support ongoing safety surveillance activities. The role generally requires self-motivation and strong organizational skills to manage tasks independently while collaborating virtually with colleagues in pharmacovigilance, clinical, and regulatory departments. Flexible work schedules and regular online meetings are common, making time management essential in a remote setting.

What are the key skills and qualifications needed to thrive as a remote drug safety associate?

To thrive as a Remote Drug Safety Associate, you need a background in life sciences, pharmacovigilance, and regulatory compliance, often supported by a relevant degree (such as pharmacy, nursing, or a related field). Familiarity with safety databases like Argus or ARISg, as well as certifications such as Drug Safety Certified Professional (DSCP), is common in this role. Strong attention to detail, clear written communication, and the ability to work independently are key soft skills. These competencies help ensure drug safety information is managed accurately and efficiently in a remote environment, contributing to patient safety and regulatory compliance.

What job categories do people searching Remote Drug Safety Associate jobs in Woonsocket, RI look for?

The top searched job categories for Remote Drug Safety Associate jobs in Woonsocket, RI are:

What cities near Woonsocket, RI are hiring for Remote Drug Safety Associate jobs?

Cities near Woonsocket, RI with the most Remote Drug Safety Associate job openings:

Remote Drug Safety Associate jobs near you
Infographic showing various Remote Drug Safety Associate job openings in Woonsocket, RI as of August 2026, with employment types broken down into 83% Full Time, 12% Part Time, and 5% Contract. Highlights an 100% Remote job distribution, with an average salary of $97,946 per year, or $47.1 per hour.

Biology Research Scientist - Remote

YO AI Labs

Boston, MA • Remote

$50 - $70/hr

Full-time

Posted 14 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?