Instagram
youtube
Facebook

Associate Ii, Pharmacovigilance

1+ years
Not Disclosed
10 April 16, 2025
Job Description
Job Type: Remote 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 II, Pharmacovigilance - UK/EU - Remote


Employer:

Worldwide Clinical Trials


Location:

United Kingdom; Homeworking (Remote)


Salary:

Competitive


Start Date:

11 April 2025


Closing Date:

11 May 2025


Job Type:

Full-Time, Remote


Company Overview:

Worldwide Clinical Trials is a global, mid-size Contract Research Organization (CRO) driven by innovation and a mission to improve lives. With over 3,500+ professionals, the organization takes a pioneering approach to drug development, focusing on creativity, excellence, and collaboration. The company is deeply committed to diversity, inclusion, and providing a workplace where professionals can thrive and be their authentic selves.


About the Pharmacovigilance Department:

The Pharmacovigilance team plays a vital role in drug safety, overseeing the lifecycle of clinical compounds from early human trials to global regulatory approvals. They manage safety events worldwide, collaborate with clients, and handle all aspects of safety reporting and regulatory submissions.


Key Responsibilities:

  • Author Safety Management Plans for assigned studies

  • Attend internal and client meetings as needed

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

  • Perform data entry into safety databases and track safety information

  • Generate and follow up on queries related to missing/unclear information

  • Conduct quality control of SAE cases processed by other team members

  • Generate regulatory reports and perform safety submissions

  • Prepare and submit periodic safety reports

  • Stay updated on safety-related regulations and guidelines


Candidate Profile – What You Will Bring:

  • Solid understanding of medical/scientific terminology, drug safety principles, and global pharmacovigilance regulations

  • Strong knowledge of database systems and data extraction techniques

  • Positive and professional demeanor in a global work environment

  • Excellent organizational skills and ability to manage multiple priorities

  • Demonstrated reliability, adaptability, and team collaboration


Qualifications & Experience:

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

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

  • Proficient with MS Office tools (Excel, PowerPoint, Word)

  • Strong verbal and written communication skills

  • High attention to detail and organizational capability


Why Join Worldwide Clinical Trials:

  • Opportunity to make a real-world impact in patients' lives

  • Supportive, inclusive culture that promotes collaboration and innovation

  • Equal opportunity employer that celebrates diversity and provides equal access to growth opportunities

  • A global environment that values different perspectives and fosters a sense of belonging


More Information:

Visit the careers page: www.worldwide.com or connect on LinkedIn to explore additional opportunities.