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...
Experienced Regulatory Affairs Assistant required for our client, a professional and leading company within its field. This is a long term temporary assignment paying around £13 per hour. You will be providing comprehensive secretarial and administrative support to a large regulatory affairs team, ensuring the department runs smoothly and efficiently during this busy time. Your main focus will be to offer the following; <b...
Experienced Business Analyst required to work within Regulatory Operations for a global and leading pharmaceutical company based in Maidenhead. This role is for an immediate start working initially on a 6 month - 3 year basis. Key to this role is: Ability to manage small projects. Excellent analytical skills. Strong problem solving skills. Previous background in pharmaceutical industry preferred. ...
Our established Pharmaceutical client based in Maidenhead is looking for a Quality Operations Executive to join their team on a 6 month contract. Job purpose: To support the management team with the release of products into the UK Supply Chain, detecting product quality defects and dealing with customer complaints related to product quality ensuring that these complaints are management and investigated appropriately. <...
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...
Our client is currently recruiting for a Financial Analyst working in the Maidenhead area. Working as part of the finance team you will be supporting the following; Financial year end processes. Auditing. Financial administration for various departments. Reconciliations. Budget analysis. The ideal candidate will be confident working in a multi matrix team supporting various department...
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...
PHARMACOVIGILANCE MANAGER,c £45000 + Good Benefits, Berkshire. 84/dh PHARMACOVIGILANCE MANAGER: JOB ROLE: Provide pharmacovigilance Advice & support to the UK, Ireland & Malta affiliates. Support Head of Pharmacovigilance To meet the company's statutory pharmacovigilance responsibilities. This is a senior position With a low level of supervision along with project responsibility and interact...
Regional Accountant-Maidenhead Covance is a leading global drug development services company and we provide support to the Pharmaceutical and Biotechnology industries. This role involves direct responsibility for ensuring complete, accurate and timely accounting, reporting and compliance for a number of European companies and branches. THIS POSITION IS A (CIRCA) 11 MONTH FIXED TERM CONTRACT. The pr...
Business Partner (Senior Finance) COVANCE is a leading global drug development services company and we provide support to the Pharmaceutical and Biotechnology industries. About the Job This Senior Manager level position is a pivotal role in our Business Analyst group. The Business Analyst group provides FP&A guidance and delivery across our Clinical Development Services business in Europe, partnering with ...
Our client is a global, broad-based health care company devoted to the discovery, development, manufacture and marketing of pharmaceuticals and medical products, including nutritionals, devices and diagnostics. Our client is now looking for someone to join them as a Regulatory Affairs Officer based in Southampton. MAIN PURPOSE: To provide regulatory advice and support to the UK Abbott affiliate...
COVANCE is a leading global drug development services company and we provide support to the Pharmaceutical and Biotechnology industries. About the Job This Senior Manager level position is a pivotal role in our Business Analyst group. The Business Analyst group provides FP&A guidance and delivery across our Clinical Development Services business in Europe, partnering with senior leaders to provide a highly regarded analysi...
Project Director - Study Start Up Maidenhead Covance, with headquarters in Princeton, New Jersey, is one of the world's largest and most comprehensive drug development services companies, with annual revenues greater than $2 billion, employees in more than 60 countries, and more than 11,000 employees worldwide. You can make a difference by helping to deliver life-saving and life-enhancing medicines to people around...
Senior Training Coordinator (circa 6 month contract) COVANCE is a leading global drug development services company and we provide support to the Pharmaceutical and Biotechnology industries. You can make a difference by helping to deliver life-saving and life-enhancing medicines to people around the world. Our commitment to this mission has resulted in Covance's impressive history of company stability and growth. We've ach...
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...
Regulatory Affairs Project Manager Our client is a global, broad-based health care company devoted to the discovery, development, manufacture and marketing of pharmaceuticals and medical products, including nutritionals, devices and diagnostics. Our client is now looking for someone to join them as a Regulatory Affairs Project Manager. Core Job Responsibilities: -Provide strategic input into the ...
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...
