You will support the Business Function HR Business Partners (HRBP) for our UK and International Hubs to effectively, proactively and accurately manage people-related admin tasks.
This role is available due to continued growth and the department's success in winning new audit business.
Audit Supervisor opportunity within practice, to join the friendly and dynamic audit & accounts team based in Maidenhead.
This is a fantastic accountancy firm that offers a friendly, supportive working environment, encourages career development and progression, offers a good benefits package, and operates flexible, hybrid working to maximise work/life balance.
From managing office schedules and coordinating meetings to handling important correspondence and assisting with a variety of administrative tasks, you'll be at the heart of our organisation.
Are you a proactive, detail-orientated individual with excellent organisational skills and a love for delivering exceptional customer service?
You'll join a role that will support our executive office, providing essential support to our leadership team, and ensuring a smooth day-to-day of operations.
My global pharmaceutical client, based in Berkshire, are looking for a Spanish Speaking Customer Service/Complaint Intake Analyst to join their team urgently initially on a 12-month basis.
Purpose
The Complaint Intake Analyst works to support PMQA through providing the initial triaging of complaints from all channels and serves as the first point of contact with the customer.
Our International Public Affairs team currently has an opportunity for an Executive Assistant based in Maidenhead, UK.
My client creates breakthrough products - in diagnostics, medical devices, nutrition and branded generic pharmaceuticals - that help you, your family and your community lead healthier lives, full of unlimited possibilities.
Today, 113,000 of our client's employees are working to make a lasting impact on health in the more than 160 countries that they serve.
SRG are currently looking for a Regulatory Affairs Manager for a Global Pharmaceutical Company who have opened a new vacancy within their Regulatory Affairs team on an initial 12 Month basis to be based at their office in Maidenhead.
The Role
Ensure the submission strategy for clinical trials planned globally are in accordance with the overarching global regulatory strategy and any risks and issues are highlighted to the Global Regulatory Project Team and study teams.
Deliver CTA regulatory strategies and operations for a designated portfolio of development compounds in specified geographic region.