At a Glance
- Tasks: Support the development of Risk Management Plans and assist with Marketing Authorisation Applications.
- Company: Quanticate International Limited, a leader in pharmacovigilance consulting.
- Benefits: Flexible zero-hour contract, work independently, and gain valuable experience.
- Other info: Ideal for independent consultants looking to manage multiple projects.
- Why this job: Make a real impact in drug safety and regulatory compliance.
- Qualifications: Strong background in pharmacovigilance and excellent writing skills.
The predicted salary is between 40 - 50 £ per hour.
Quanticate International Limited is looking for an experienced Pharmacovigilance Consultant to provide specialized support in developing and maintaining Risk Management Plans (RMPs). This role offers a zero-hour contract and is perfect for an independent consultant with extensive regulatory and pharmacovigilance expertise. You will play an essential role in supporting Marketing Authorisation Applications (MAAs) and post-approval activities.
The ideal candidate will have a strong background in pharmacovigilance, excellent writing skills, and the ability to work independently while managing multiple projects.
Global Pharmacovigilance Risk Management Consultant employer: QUANTICATE INTERNATIONAL LIMITED
Quanticate International Limited is an exceptional employer that values the expertise of its consultants, offering a flexible zero-hour contract that allows for independence and work-life balance. With a strong focus on professional development, employees are encouraged to enhance their skills in a supportive environment, while contributing to impactful projects in pharmacovigilance. Located in a dynamic industry, this role provides unique opportunities to engage with regulatory processes and make a meaningful difference in patient safety.
Contact Details:
QUANTICATE INTERNATIONAL LIMITED Recruitment Team
