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Associate, Pharmacovigilance

1+ years
Not Disclosed
10 July 18, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc/B.Pharm/M.Pharm/Life Science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

 

Job Title:

Associate, Pharmacovigilance

Location:

Remote – United States

Company:

Worldwide Clinical Trials

Compensation:

Competitive (not specified in the job description)


Job Summary

Worldwide Clinical Trials is hiring a Pharmacovigilance Associate to join their remote team in the United States. This is an excellent opportunity for professionals with at least 1 year of PV experience in pre-approval clinical trials to contribute to global drug safety operations. You’ll be part of a forward-thinking, midsize CRO known for innovation, scientific rigor, and a patient-centric approach to clinical development.


Key Responsibilities

  • Author Safety Management Plans for assigned studies

  • Attend and present in internal, client, and Investigator Meetings

  • Review Serious Adverse Events (SAEs) for accuracy and completeness

  • Enter safety data into the database and maintain tracking records

  • Query and follow up with clinical sites for missing safety data

  • Perform Quality Control checks on processed SAEs

  • Generate regulatory reports and perform safety submissions

  • Prepare and submit periodic safety reports

  • Stay up-to-date with safety regulations and guidelines

  • Monitor project scope and escalate issues as needed

  • Assist in bid defenses, training, or mentoring new PV staff


Required Skills & Qualifications

  • Bachelor's degree in a science-related field, nursing, or equivalent

  • Minimum 1 year of pharmacovigilance experience (pre-approval trials)

  • Familiarity with medical terminology, clinical AE assessment, and global PV regulations

  • Proficiency in MS Office (Excel, PowerPoint, Word)

  • Strong written and verbal communication skills

  • Detail-oriented with excellent organizational abilities

  • Capable of managing multiple priorities within deadlines

  • Comfortable working independently and in a matrix team environment

  • Willingness to travel occasionally for meetings (domestic/international)

  • Fluent in English (written and spoken)


Perks & Benefits

  • 100% Remote work flexibility within the US

  • Work with innovative, science-driven CRO projects

  • Inclusive and supportive workplace culture

  • Career development and cross-functional collaboration opportunities

  • Opportunity to support global regulatory submissions and drug safety


Company Description

Worldwide Clinical Trials is a global, mid-sized Contract Research Organization (CRO) with over 3,500 experts delivering high-quality clinical development services. Focused on innovation and therapeutic impact, Worldwide is a leader in patient-centric trials and drug safety operations, partnering with sponsors to advance medical breakthroughs.


Work Mode

Remote – USA


Call-to-Action

Ready to make a difference in global drug safety? If you’re passionate about pharmacovigilance and seeking a flexible, mission-driven role, apply now and become part of a company that’s reimagining the future of CROs.

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