Manage collection, documentation, and reporting of adverse events from various sources (clinical trials, literature, spontaneous reports).
Ensure timely data entry and compliance with internal procedures.
General
Currently working with a Global Pharmaceutical company who are looking for an experienced Patient Safety Specialist to support patient safety operations, ensuring compliance with global and local regulations for vigilance of marketed and investigational products (drugs, supplements, medical devices).
Posted by Michael Page Property & Construction • £72K/yr to £90K/yr
General
Key management role representing Global Security and Safety by providing advice and solutions that mitigate operational, strategic, and tactical security risks and works in collaboration with a wide range of internal and external partners
Large global supplement brand with a presence world wide and in the UK.
Description
Be the subject matter expert and main point of contact for all security matters and related programs in EMEA and India and deliver top-level service.
PDC are a market-leading company with a strong portfolio of brands.
What you can expect from a role with us is flexibility, autonomy with no micromanagement, supportive managers and peers, and opportunities to progress.
We believe people are our biggest asset, and our company culture reflects that.
Posted by Hays Specialist Recruitment Limited • £50/hr to £58/hr
Your new company
This position will sit within the global regulatory team and will require someone to have both development and post-marketing experience.
Global Biotechnology in the UK are looking for a Regulatory Affairs Manager to develop and implement regulatory strategies for EU markets for their Oncology portfolio.
Connect with new referrals, building a strong rapport and understanding individual insurance requirements.
General
Are you a motivated and ambitious individual looking for an exciting career in the insurance and claims industry?
Join our dynamic team, where you'll be responsible for connecting with clients, understanding their insurance needs, and providing them with exceptional support throughout their claims journey.
Working with the regulatory team (and core stakeholders across multiple areas), your role will be to provide regulatory strategy and guidance across the region and make sure that regulatory deadlines and approvals are achieved.
An innovative global pharmaceutical company is currently looking for a Regulatory Affairs Manager with CTA, EU and early stage development experience to join their team on a 12 month temporary contract.
Other responsibilities include
You will develop, contribute and ensure the accurate preparation of high-quality regulatory documents needed to support clinical trials and medical products.
Posted by GPD Healthcare Limited T/A ThinkWorkForce • £75/hr to £80/hr
Department: Urgent Care
The UTC supports the Emergency Department (ED), allowing the ED to focus on life-threatening conditions.
Our client operates an award-winning Urgent Treatment Centre (UTC) designed to provide exceptional care for patients with minor injuries and illnesses.
Will have experience of working on the phones in an office environment, managing incoming and outgoing calls as well as emails.
This is a fantastic opportunity to work for a dynamic, fast moving company within the credit hire industry who pride themselves not only on brilliant service to their customers but also maintaining an enviable place to work.