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.
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