Regulatory Affairs Associate Director. Therapeutically focused in Oncology. Permanent
Are you a senior Regulatory professional seeking to take the next step up in your Regulatory Affairs Career? If so, I have a fantastic permanent Regulatory Associate Director role available with a leading global pharmaceutical/R&D company located in London!
As Senior Regulatory Affairs Associate, responsibility will be covering lifecycle activity within the EU, Emerging and African regions for a blockbuster product and other specialist therapy areas. Including; the preparation, submission and review of CTAs, MAAs, IMPD, PIPs. This role will suit a candidate with relevant experience looking for an organisation to develop within.
Take Responsibility for defining regulatory strategies and submissions in support of new and existing marketing authorisations & Receive excellent training and real career development for an Ethical Branded Pharmaceutical company. Contact Theo Moore on +44 207 801 3394 or email your cv to CV@advrgeulatory.com
I’m searching for Senior Regulatory Affairs Associates to work for a global specialty pharmaceutical company. Based in the West Midlands
Within this role your main areas of responsibilities will include the following areas:
• Project management of European (MRP’s, CP’s, NCE) and World-wide regulatory projects. • Preparing registration strategies as appropriate. • Provide advice and determine appropriate action for proposed manufacturing/license changes. ...
Full job description and company details are available upon application, apply below. This position is being dealt with by Rachael Matthews at Meet, call on + 44 203 178 7488 or +44 77 9441 1452 or via e-mail directly at Rachael@peoplewithchemistry.com to discuss in confidence.
Senior Manager / Associate Director Regulatory Affairs is required to join a growing global Biopharmaceutical company based in the South East on permanent basis. My client has an excellent product portfolio and exciting pipeline focussed on life-threatening illnesses. This role is responsible for the entirety of my clients market leading therapy portfolio and offers the successful candidate high levels of autonomy, visibility, challenge and the chance to make a difference.
Senior Regulatory Officer/Team Leader - Global Pharmaceutical - regulatory compliance - up to £50,000
Senior Regulatory Officer/Team Leader - Global Pharmaceutical - regulatory compliance - up to £50,000
We are currently working with a leading worldwide organisation that provides development and commercial manufacturing to global pharmaceutical, biotechnology and specialty pharmaceutical companies.
Regulatory Affairs Associate
Leading global specialist healthcare company is looking for an experienced Regulatory Affairs Associate for their growing UK offices in Surrey due to further expansion. This fast paced global specialist healthcare company is seeking talented individual to join their team. The company strives to serve patients by transforming the promise of science into therapies that have the power to restore health or even save lives.
Join a leading Pharmaceutical company in a leadership role where you will be the regulatory lead for products coming through the development lifecycle. This is exciting role where you will develop regulatory strategies and work as the lead as your project goes from mid or late stage development through to filing. Contact Theo Moore or Matt Greig for more details on 0207 801 3384 or email theo@advregulatory.com in confidence.
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