Instagram
youtube
Facebook

Associate Ii, Pharmacovigilance - Uk/Eu - Remote

1+ years
Not Disclosed
10 May 19, 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

Associate II, Pharmacovigilance - UK/EU - Remote

Employer: Worldwide Clinical Trials
Location: United Kingdom (Remote)
Salary: Competitive
Start Date: 10 May 2025
Closing Date: 9 June 2025

About the Company:
Worldwide Clinical Trials is a midsize, global CRO dedicated to pushing boundaries in the development of life-saving treatments. With over 3,500 professionals, they combine innovation with high-quality execution across all aspects of clinical research. Their culture values diversity, inclusion, and authentic collaboration—where individuals thrive by being themselves.

Pharmacovigilance at Worldwide:
The Pharmacovigilance team is integral to drug safety and the clinical development lifecycle—from first human administration through global approval. The team reviews global safety data and collaborates with clients on regulatory reporting, ensuring patient protection and compliance.

Key Responsibilities:

  • Author and maintain Safety Management Plans for assigned studies

  • Participate in internal and client-facing meetings as needed

  • Review incoming Serious Adverse Event (SAE) data for completeness and accuracy

  • Enter data into the safety database and track safety information

  • Generate and resolve queries for incomplete or unclear SAE reports

  • Perform quality control (QC) checks of SAEs processed by other team members

  • Prepare and submit regulatory and periodic safety reports

  • Ensure all submissions meet regulatory requirements and timelines

  • Stay updated on relevant safety regulations and guidelines

Skills and Knowledge Required:

  • Strong knowledge of medical and scientific terminology

  • Familiarity with clinical safety reporting requirements and global PV regulations

  • Proficiency in safety databases and data management

  • Detail-oriented with strong organizational and multitasking skills

  • Excellent written and verbal communication skills

  • Professional and diplomatic interpersonal skills in a global team environment

  • Adaptability, reliability, and a collaborative mindset

Qualifications and Experience:

  • Bachelor’s degree in life sciences, nursing, or related field (or equivalent experience)

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

  • Strong command of MS Office (Excel, PowerPoint, Word)

  • Excellent attention to detail and ability to meet deadlines

Join a Mission That Matters:
At Worldwide, your work contributes directly to improving lives. The company fosters a workplace where all individuals, regardless of background, are empowered and supported to succeed.

To Apply or Learn More:
Visit
www.Worldwide.com or explore their careers page for additional roles.