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.
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