Technical Support Specialist - UV Location: Nr, High Wycombe , Bucks REF : MS 111581 Salary: £26,000- 32,000 + Bens My client is an international healthcare provider of a variety of scientific instruments used in clinical, env...
The Company: We are working on behalf of a group of healthcare communications companies. The group consists of medical education, advertising and public relations. They have modern offices in London and North of London. This role is to be based north of London (Herts/Bucks) in the medical education division. There is a very strong senior management team and plans for growth in 2012. The Role: Reporting to th...
The Company: Established for decades and currently experiencing very strong growth over the last few quarters. This is a pharmaceutical company with a global presence. They work across pharmaceuticals, OTC Products, Devices and other areas. The company employs thousands of professionals around the world. The Role: This 12 month, Clinical Manager position within the Urology area will cover the European Unio...
Our client in Marlow is looking for a candidate that has experience as a Product or Brand Manager in Spain. You will be directly responsible for effective and timely implementation of national tactical plans for Spain’s Neurosciences Business Unit. Working alongside the BUD and the Sales Programs Manager, the P&P Manager is required to have strong operational and project-management skills to ensure that the tactical programs are ...
THE COMPANY Global, extremely well known and sought after professional Pharmaceutical company based in High Wycombe. THE ROLE To provide Team Admin support in a professional, busy and high profile department Updating and producing various reports Managing a busy diary system Typing letters, memos and emails Dealing with queries Responding to request for information Updating logs U...
This is a Temporary role (minimum of 3 months) – please be aware of this when applying. Working Hours: 9:00am – 5:00pm Some of the main areas of responsibility: - To provide business analyst support for the company. - Send out bi-monthly/monthly tracking models and liaise with EMEA country heads. - Receive and process patient tracking returns. - Ident...
Job Description Job Description Adverse event case entry, coding and narrative writing Assist in regulatory assessment of adverse events and submission to relevant authorities Participate in specific projects as directed by line management Participate in client meetings and liaise with clients regarding ongoing projects as required Ensure compliance with EU regulatory requ...
The Company: Established for decades and currently experiencing very strong growth over the last few quarters. This is a pharmaceutical company with a global presence. They work across pharmaceuticals, OTC Products, Devices and other areas. The company employs thousands of professionals around the world. The Role: Will support the implementation of regulatory operational activities in Emerging Markets in E...
The Company: An international medical communications company. They cover healthcare advertising, medical education, public relations, market access and has an in-house digital team. The company has offices based on two continents with multiple sites in the UK. They have a diverse client base of pharmaceutical and biotechnology companies. The Role: This is a maternity cover for 6 to 12 months. It will work ...
Procurement Coordinator Fixed term 12 month contract Amazing opportunity to work for a well known company based near Marlow. The purpose of the role is to provide support to Procurement and Supply Chain functions. Assist with planning and management of stock. Responsibility’s will include: Assisting in drafting tender documents Market analysis Benchmark supplier offers against other tender specifications</p...
Our client is a forward thinking, Global Clinical Research Organisation who have an exciting opportunity for a Senior Regulatory Manager on a permanent bases. As part of Global Regulatory Affairs you will work in the EU and Asia-Pacific Regulatory team, you will form part of a successful and driven team that provides consultancy for all projects globally as well as stand alone contracts with clients. Responsibilities: </p...
Our client is a forward thinking, Global Clinical Research Organisation who have an exciting opportunity for a Senior Regulatory Manager on a permanent contract . As part of Global Regulatory Affairs you will work in the EU and Asia-Pacific Regulatory team, you will form part of a successful and driven team that provides consultancy for all projects globally as well as standalone contracts with clients...
JOB DESCRIPTION - Medical Writer Reporting to : Associate Divisional Director Principal Role: You are responsible for (a) researching and developing technical material, (b) ensuring that all output adheres to written brief, is accurate in content and editorial style and can be referenced, (c) liaising with clients and key opinion leaders on content development either through th...
