ZipRecruiter

Log In

2

Remote Drug Safety Associate Jobs in Oregon (NOW HIRING)

Med Communications

Pharmacovigilance Physician

Remote (United States) Department: Pharmacovigilance Reports To: Global Head of Pharmacovigilance and Drug Safety Employment Type: Contractor Join our Team Med Communications is seeking a ...

New

NV5

Remote Sensing Technician

Comply with all policies and procedures developed for safety and operations in dynamic environment ... check and drug screening. NV5 offers competitive compensation and benefits package including ...

(ISC)2

Customer Experience Associate - Remote

$14.50 - $20/hr

Our charitable arm, the Center for Cyber Safety and Education, enables ISC2 and our members to ... This is a remote role. **This position is not available to residents of California*

Solvenow Inc.

Electrical Designer

Hillsboro, OR · On-site +1

... remote environments. Ideally, you'll also have: * Two-year Associate's Degree in relevant field ... Must pass a background check and drug screening and be fully authorized to work in the U.S. (no ...

Groups Recover Together, Inc.

Entitlement Specialist

$19 - $25/hr

Fully Remote work (Not available to residents of: AK, AR, CA, HI, ID, MD, NE, SD, UT, WY). This ... Associate's degree or higher, preferably in social services, human services, or a related field.

next page

Showing results 1-20

All JobsDrug Safety Associate JobsRemote Drug Safety Associate JobsRemote Drug Safety Associate Jobs in Oregon

Remote Drug Safety Associate information

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 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 are popular job titles related to Remote Drug Safety Associate jobs in Oregon? For Remote Drug Safety Associate jobs in Oregon, the most frequently searched job titles are:
What job categories do people searching Remote Drug Safety Associate jobs in Oregon look for? The top searched job categories for Remote Drug Safety Associate jobs in Oregon are:
What cities in Oregon are hiring for Remote Drug Safety Associate jobs? Cities in Oregon with the most Remote Drug Safety Associate job openings:
Remote Drug Safety Associate jobs near you

Pharmacovigilance Physician

Med Communications

Remote

Full-time

Posted 3 days ago

New

Job description

Pharmacovigilance Physician
Location: Remote (United States)
Department: 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 equivalent) to provide medical expertise in the evaluation and interpretation of safety data for pharmaceutical products. This role is responsible for medical review of individual case safety reports, aggregate safety assessments, signal detection activities, benefit-risk evaluations, and support of regulatory safety reporting requirements. The Pharmacovigilance Physician serves as a key medical resource for client safety activities and collaborates with clients, regulatory authorities, and internal teams to support pharmacovigilance compliance and patient safety.
What You'll Do
As our Pharmacovigilance Physician Contractor you will:
Safety Review and Medical Assessment
  • Conduct medical review of individual case safety reports (ICSRs) and provide medical assessment statements.
  • Review and interpret clinical trial and post-marketing safety data.
  • Perform benefit-risk analyses and medical assessments for client products.
  • Evaluate aggregate safety information for periodic safety reports and ad hoc requests.
  • Support safety signal detection, evaluation, and verification activities.
Pharmacovigilance Support
  • Support pharmacovigilance systems for Med Communications and client programs in accordance with contractual requirements.
  • Integrate regulatory and compliance requirements into medical assessment activities.
  • Assist and support the Qualified Person for Pharmacovigilance (QPPV), as required.
Client and Regulatory Collaboration
  • Lead and participate in client safety meetings.
  • Provide medical expertise during interactions with safety monitoring boards and regulatory authorities.
  • Represent client interests in safety-related discussions when appropriate.
Medical and Regulatory Documentation
  • Assist in drafting, reviewing, and refining medical sections of:
    • Periodic Adverse Drug Experience Reports (PADERs)
    • Periodic Safety Update Reports (PSURs)
    • Development Safety Update Reports (DSURs)
    • Periodic Benefit-Risk Evaluation Reports (PBRERs)
    • IND Annual Reports
    • Investigator's Brochures (IBs)
    • Integrated Summary of Safety (ISS) documents
    • U.S. and international product labeling documents
    • Regulatory authority safety information requests
  • Assist with drafting, reviewing, and refining risk management plans and risk evaluation and mitigation strategies when required by client contracts.
What We're Looking For
Education
Either:
  • Licensed Medical Physician (MD, DO, or equivalent) in good standing in applicable state(s) of licensure. Board certification in a therapeutic area relevant to client programs is preferred.
Or:
  • Unlicensed Medical Physician (MD, DO, or equivalent) with no record of past or present Medical Board disciplinary action and at least five (5) years of combined pharmacovigilance experience, clinical healthcare provider experience, or equivalent experience.
Preferred:
  • Degree or training in Epidemiology.
Experience
  • Minimum of five (5) years of pharmacovigilance experience in the pharmaceutical industry or equivalent experience, including:
    • Clinical trials investigator
    • Health authority inspector
    • Epidemiologist
    • Other related healthcare or drug safety roles
Knowledge, Skills, and Abilities
Technical Knowledge
  • Understanding of pharmacovigilance regulations and compliance requirements from:
    • U.S. Food and Drug Administration (FDA)
    • European Medicines Agency (EMA)
    • Japan Pharmaceuticals and Medical Devices Agency (PMDA)
    • United Kingdom Medicines and Healthcare products Regulatory Agency (MHRA)
    • International Council for Harmonisation (ICH)
Computer Skills
  • Proficiency with Microsoft Office applications preferred.
  • Experience with content management systems preferred.
Why Join Med Communications?
Join a collaborative team dedicated to supporting clients with high-quality pharmacovigilance services and maintaining a strong commitment to patient safety, regulatory compliance, and scientific excellence.
Med Communications is an Equal Opportunity Employer and is committed to fostering a diverse and inclusive workplace.

Apply