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- Tasks: Join our Pharmacovigilance team to ensure drug safety and support clinical trials.
- Company: Worldwide Clinical Trials is a global CRO dedicated to innovative drug development.
- Benefits: Enjoy remote work, a diverse environment, and opportunities for personal growth.
- Why this job: Make a real impact on patient lives while working in a supportive and inclusive culture.
- Qualifications: Bachelor's degree in a science-related field and at least 1 year of pharmacovigilance experience required.
- Other info: We value creativity and collaboration, welcoming diverse talent to thrive.
The predicted salary is between 28800 - 48000 £ per year.
Associate II, Pharmacovigilance – UK/EU – Remote
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Who We Are We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence. We are Worldwide Clinical Trials, a global team of over 3,500+ experts working to change the way the world experiences CROs – in the best possible way. Our mission is to work with passion and purpose every day to improve lives. We value diversity and inclusion and strive to enable professionals from all backgrounds to succeed.
What Pharmacovigilance Department Does At Worldwide Pharmacovigilance is the gateway to ensuring drug safety. Our Pharmacovigilance team comprises a dynamic group with extensive experience within the Drug Safety world. We review safety events from all over the world and work with our clients to review, analyze, and submit to Investigators, Ethics Committees/IRBs, and Regulatory Agencies furthering clinical drug development.
What You Will Do
- Author Safety Management Plan for assigned studies
- Attend internal and client meetings as appropriate
- Review incoming SAE data for completeness and accuracy
- Perform data entry in the Safety Database and/or complete applicable tracking of incoming safety information
- Generate queries for missing or unclear information and follow-up with sites for resolution
- Perform QC of SAEs processed by other PV Associates
- Generate regulatory reports and perform safety submissions as needed
- Prepare and submit periodic safety reports as needed
- Maintain knowledge and understanding of safety related regulations and guidelines
What You Will Bring To The Role
- Good understanding of medical and scientific terminology, of the principles of clinical assessment of adverse drug events, of international regulations and of reporting requirements
- Good understanding of computer technology, and management of relational database systems, including extraction of data
- Positive attitude and ability to interact diplomatically and professionally with internal and external customers in a global environment
- Excellent organization skills and ability to handle multiple competing priorities within tight timelines. Consistently demonstrates commitment, dependability, cooperation, adaptability and flexibility in executing daily tasks and responsibility
Your Experience
- Bachelor’s degree in a science-related field, nursing, or equivalent
- Minimum of 1 year of pharmacovigilance experience (pre-approval clinical trials)
- Equivalent combination of relevant education and experience
- Computer literacy and strong working knowledge of MS Office applications (Excel, PowerPoint, Word)
- Excellent written and verbal communication skills
- Excellent organization skills and attention to detail
Worldwide is an equal opportunity employer that is committed to enabling professionals from all backgrounds and experiences to succeed and to that end we prioritize attracting diverse talent and cultivating an inclusive environment. We provide equal employment opportunities to all employees and applicants regardless of race, color, ethnicity, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or other class protected by applicable law.
Seniority level
- Entry level
Employment type
- Full-time
Job function
- Research, Analyst, and Information Technology
- Industries
- Research Services
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Associate II, Pharmacovigilance - UK/EU - Remote employer: Worldwide Clinical Trials
Contact Detail:
Worldwide Clinical Trials Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Associate II, Pharmacovigilance - UK/EU - Remote
✨Tip Number 1
Familiarise yourself with the latest pharmacovigilance regulations and guidelines. This knowledge will not only help you in interviews but also demonstrate your commitment to the field and understanding of the role.
✨Tip Number 2
Network with professionals in the pharmacovigilance sector, especially those who work at Worldwide Clinical Trials. Engaging with them on platforms like LinkedIn can provide insights into the company culture and expectations.
✨Tip Number 3
Prepare to discuss specific examples from your past experience that showcase your ability to handle multiple priorities and tight deadlines. This is crucial for demonstrating your organisational skills during the interview.
✨Tip Number 4
Showcase your computer literacy by being ready to discuss your experience with database systems and MS Office applications. Highlight any specific projects where you used these tools effectively to manage data or reports.
We think you need these skills to ace Associate II, Pharmacovigilance - UK/EU - Remote
Some tips for your application 🫡
Understand the Role: Before applying, make sure you thoroughly understand the responsibilities and requirements of the Associate II, Pharmacovigilance position. Familiarise yourself with pharmacovigilance concepts and the specific tasks mentioned in the job description.
Tailor Your CV: Customise your CV to highlight relevant experience in pharmacovigilance or related fields. Emphasise your understanding of medical terminology, data management skills, and any previous roles that involved regulatory compliance or safety reporting.
Craft a Compelling Cover Letter: Write a cover letter that reflects your passion for improving lives through drug safety. Mention specific experiences that demonstrate your ability to handle multiple priorities and your commitment to quality and excellence in your work.
Proofread Your Application: Before submitting, carefully proofread your CV and cover letter for any spelling or grammatical errors. A polished application reflects your attention to detail, which is crucial in the pharmacovigilance field.
How to prepare for a job interview at Worldwide Clinical Trials
✨Understand the Role
Make sure you have a solid grasp of what the Associate II, Pharmacovigilance role entails. Familiarise yourself with key responsibilities like authoring Safety Management Plans and reviewing SAE data. This will help you answer questions confidently and demonstrate your genuine interest in the position.
✨Showcase Your Experience
Be prepared to discuss your previous pharmacovigilance experience in detail. Highlight specific projects or tasks you've worked on that relate to drug safety and regulatory submissions. Use examples to illustrate your skills in handling multiple priorities and working under tight timelines.
✨Demonstrate Communication Skills
Since the role involves interaction with internal and external customers, practice articulating your thoughts clearly and professionally. Prepare to discuss how you've effectively communicated complex information in past roles, especially in a global environment.
✨Emphasise Adaptability
The pharmacovigilance field can be fast-paced and ever-changing. Be ready to share examples of how you've adapted to new challenges or changes in your work environment. This will show your potential employer that you can thrive in their dynamic team.
