This is an excellent opportunity for an experienced Clinical Trial Submissions Manager to join a global pharmaceutical company for an initial 12 months with the potential for this to be extended.
This role has come about due to expansion and an increase in the production of pharmaceutical.
My client, a prominent player in the healthcare industry, is renowned for developing groundbreaking products in diagnostics, medical devices, nutrition, and branded generic pharmaceuticals.
Contract Duration: 12 months initially, potential for permanent work afterwards
With a global workforce of 114,000 employees spread across more than 160 countries, they are committed to making a lasting impact on health.
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.
General
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.
In this role, you'll play a pivotal part in our tender submission process, working closely with Contracts Managers across the country to deliver accurate and timely bids.
We're seeking a proactive and detail-oriented Contract Specialist to join our dynamic team at our Maidenhead office.
Are you ready to take the lead in securing critical business contracts?
Are you a charismatic and passionate Content Manager full of energy and new ideas?
We are seeking an ambitious self-starter to lead our clients' primarily B2C content strategy, leveraging a commercial eye, storytelling skill, and a deep love for words.
This is your opportunity to join an established Marketing Agency in a creative role where you can make a significant impact.
This role has come about due to expansion and an increase in the production of pharmaceutical.
This is an excellent opportunity for an experienced Clincial Trial Regulatory Specialist to join a global pharmaceutical company for an initial 12 months with the potential for this to be extended.