Senior Pharmacovigilance Scientist

Job Advertisement: Senior Pharmacovigilance Scientist

Location: Welwyn Garden City
Contract Type: Temporary (12 months)
Hourly Rate: 33.98 - 37.75

Are you a passionate expert in pharmacovigilance looking for your next challenge? Join our client's dynamic Central Operations team as a Senior Pharmacovigilance Scientist! This is an exciting opportunity to make a real impact on patient safety while working in a vibrant and innovative environment.

About Us
Our team is dedicated to utilizing our pharmacovigilance expertise to ensure high-quality, compliant processing and reporting of safety data. We believe in looking beyond job titles to foster a mindset focused on the broader goal of protecting patients' safety.

Your Role
As a Senior Pharmacovigilance Scientist, you will:

• Lead and oversee ICSR case processing, ensuring compliance with regulations and standards.
• Act as an accountable leader, driving proactive process development and issue management.
• Maintain a quality mindset by devising strategies to contain issues and mitigate risks.
• Manage relationships with service providers through effective oversight and analysis.
• Communicate complex ideas clearly to colleagues and external stakeholders, especially during regulatory inspections.
• Make independent, compliant decisions while thinking critically about the bigger picture.

What We're Looking For
We are seeking someone who embodies the following qualities:

• Expertise: Profound knowledge of ICSR case processing and international regulations (ICH, EU GVP Modules, FDA).
• Leadership: Proven experience in leading complex, time-sensitive projects with a diverse range of stakeholders.
• Adaptability: Ability to handle ambiguity and reprioritize tasks to focus on impactful work.
• Team Player: A supportive colleague who thrives in both co-located and virtual teams.
• Continuous Learner: A self-motivated individual eager to explore new data sources and innovative solutions, including the use of artificial intelligence tools.

Qualifications & Experience

• Undergraduate degree or equivalent advanced learning; on-the-job pharmacovigilance experience is highly valued.
• Experience in pharmacovigilance legislation and a good understanding of the pharmaceutical industry.
• Knowledge of medical device processing is desirable.

Daily Responsibilities
In your role, you will:

• Oversee service providers executing ICSR tasks and medical device reports.
• Address queries and share your subject matter expertise proactively with stakeholders.
• Conduct process reviews to implement improvements.
• Identify root causes of non-compliance and lead the implementation of Corrective Actions and Preventative Actions (CAPAs).
• Assess the impact of new regulatory requirements on your area of expertise.

Why Join Us?
This is more than just a job; it's a chance to contribute to a mission that matters! You will be part of a passionate team dedicated to enhancing patient safety. With a competitive hourly rate and the opportunity to work on impactful initiatives, this role is perfect for someone looking to grow and thrive in their career.

Ready to Make an Impact?
If you're excited about this opportunity and believe you have what it takes to excel as a Senior Pharmacovigilance Scientist, we want to hear from you! Apply now to join our client's mission to safeguard patient safety and be part of an energetic and innovative team!

Our client is an equal opportunity employer and values diversity in the workplace. We encourage applications from all qualified individuals.

We use generative AI tools to support our candidate screening process. This helps us ensure a fair, consistent, and efficient experience for all applicants. Rest assured, all final decisions are made by our hiring team, and your application will be reviewed with care and attention.

Adecco is a disability-confident employer. It is important to us that we run an inclusive and accessible recruitment process to support candidates of all backgrounds and all abilities to apply. Adecco is committed to building a supportive environment for you to explore the next steps in your career. If you require reasonable adjustments at any stage, please let us know and we will be happy to support you.