There is an excellent opportunity available within a Quality Analyst role at a small but growing medical device firm. Working within the Quality Analyst role, you will be responsible for supporting the Quality management system and ensuring accurate completion of all tasks related to complaint records. In addition, you will be working closely with the Engineering, QC, Materials, and Manufacturing department. ...
Medical Manager / Associate Medical Director - International Company
Our client is an extremely successful pharmaceutical company focusing within Haematology, Diabetes and Hormone therapy. The company is currently operating in 75 countries worldwide and is employing in excess of 30,000 people.
A position has arisen to be based in their Zurich branch which is a very exciting opportunity for an experience Medical Manager who is looking to take the step in their career. ...
My client is a leading International Pharmaceutical Company who is currently recruiting for a Medical Director for their clinical development Rheumatology operation in Switzerland. As a Medical Director of Rheumatology, you will be responsible for overseeing numerous projects across Europe within the Rheumatology Therapy area.
Senior Regulatory Affairs Specialist - Medical Diagnostics
A fantastic Regulatory Affairs Specialist role has come up with our client based in the German speaking part of Switzerland, within the canton of Zurich. It will be your role within this opportunity to work on exciting international projects across a range of innovative devices. As this is a fairly young company, you will get to be directly part of driving their future success.
Principal Consultant - Pharma Strategy Consultancy - C.£110K
Company:Real Staffing Location: London Salary: 100,000+ Benefits: Pensions, Healthcare, Bonus
Closing Date: 19 Jun 13
* Develop and/or elevate new business opportunities through the identification of follow-on work and new leads * Seek out and identify new revenue opportunities at existing and potential clients * Act as principal owner of client engagements with ultimate responsibility for client satisfaction and deliver high levels of quality/added value * Take the lead proposal development to ensure actionable, on-target and timely proposals are provided to clients.
Senior Manager Regulatory - Ad Promotion
Company:Real Staffing Location: Boston Salary: 100,000+
Closing Date: 19 Jun 13
Job Description:
The Senior Manager in Regulatory Affairs, Advertising and Promotions is responsible for providing strategic and operational leadership in the area of advertising and promotion focused toward US marketing activities and products across numerous therapeutic areas. The Senior Manager will review promotional materials to assess for compliance with the applicable regulations and guidance documents.
Freelance Statistician - 6 Months rolling contract
My client is one of the largest HEOR consultancies in the world who, due to on going growth and development, are looking to appoint a new associate director of market access. In this position you will be responsible for managing a group of market access consultants as well as developing new business and managing existing clients.
Lead/Senior Health Data Scientist – US, Europe and Asia
An opportunity has arisen to become a part of the senior leadership team within a fast growing and highly successful consultancy that are currently looking to expand their Real World Evidence team. They have direct access to some of the best resources in the market place and deliver excellent insights to product effectiveness, safety, epidemiology and health economic outcomes. Do you feel as though you have gone as far as possible with your current employer? Then this position is for you?
My client is a global pharmaceutical company who are currently undergoing massive expansion in their global medical function. As a Study Medical Expert you will be responsible for the development and execution of thrombosis studies. As such you will be the internal medical charged with developing clinical protocols, taking part in study initiation and training staff on all medical aspects of the studies.
Vice President of Account Services
Company:Real Staffing Location: New York Salary: 100,000+
Closing Date: 18 Jun 13
Vice President Business Development
My client is a global medical communciations agency seaking a Vice President of Business Development in the New York area. They have a long history of delivering strategic and tactical medical communication programs including: Advisory boards, KOL Identification/Mapping, Live Events, Educational Material and publication planning.
Product Manager- Neurosciences
Company:Gold Group Location: Geneva Salary: 100,000+ Benefits: Benefits
Closing Date: 28 May 13
Specialist Bio pharmaceutical company are offering a fantastic opportunity for an experienced Product manager to join them in their offices in Switzerland.
Contract SAS Programmer - Global Biotech - Home Based
Company:Skills Alliance Location: Home Based Salary: 100,000+
Closing Date: 18 Jun 13
Contract SAS Programmer:
A brand new contract SAS Programmer role has just been released by my Biotech client that can be predominantly home based:
SENIOR SAS...
Medical Science Liaison - Respiratory - Sydney $100 - $150K
Company:Real Staffing Location: Sydney Salary: 100,000+ Benefits: car, bonus, super
Closing Date: 18 Jun 13
Medical Science Liaison/ Medical Affairs Specialist within Respiratory or any related disease to join a top global Pharma company office based in Sydney Australia.
Salary - $100 - $130K plus $20K car allowance 10% super, healthcare and bonus. This role will be in the Sydney office with travel as and when required national and international.
Global Marketing Manager
Company:Gold Group Location: Switzerland Salary: 100,000+ Benefits: Benefits
Closing Date: 28 May 13
This is an excellent opportunity to work for a Global Medical Devices company; a leader within their particular field, offering top solutions to research and development.
Global Product Manager
Company:Gold Group Location: Switzerland Salary: 100,000+ Benefits: Benefits
Closing Date: 28 May 13
This is an excellent opportunity to work for a Global Medical Devices company; a leader within their particular field, offering top solutions to research and development.
Requirements: 1. Support and oversee all the quality and compliance processes 2. Manage and improve CAPA processes 3. Identify and design improvement processes 4. Liaising with Health Authorities regarding questions and queries 5. Driving and managing global quality plan and timely and efficiently execution 6. Closely cooperation with other involved departments and teams 7. Working and improving SOP according to GCP guidelines 8. ...
Medical Director, Oncology (€120,000 basic) Germany – Clinical Development
In this new exciting role you will: • Work with one of the largest global Pharmaceuical companys • Be the key leader in driving the Oncology division • Be the leading expert of your therapeutic area • Make a foot print on Europe • A very competitive salary well over €100k car & pension • Up to 20% bonus and Private medical Insurance. • Office based
Medical Director, Oncology (€120,000 basic) – Clinical Development
In this new exciting role you will: • Work with one of the largest global Pharmaceuical companys • Be the key leader in driving the Oncology division • Be the leading expert of your therapeutic area • Make a foot print on Europe • A very competitive salary well over €100k car & pension • Up to 20% bonus and Private medical Insurance. • Office based
Senior Medical Director - Manchester £100,000 basic
An opportunity has arisen to become a part of the senior leadership team within a fast growing and highly successful consultancy that are currently looking to expand their Real World Evidence team. They have direct access to some of the best resources in the market place and deliver excellent insights to product effectiveness, safety, epidemiology and health economic outcomes. Do you feel as though you have gone as far as possible with your current employer? Then this position is for you?
DIRECTOR REGULATORY, EU REGIONAL HEAD - BIOTHERAPEUTICS!!
Company:Key People Limited Location: Berkshire Salary: 100,000+ Benefits: Significant package
Closing Date: 27 May 13
Superb role for an accomplished Regulatory Affairs Director/Senior Director with expertise in Biologics and Biosimilars. A Biologics/Biosimilars background is essential for this role, along with Line management and an EU perspective. EU/Global Regulatory Strategy and full pipeline working knowledge. Based in the UK or France.
A Leading Biotech Company are presently looking to bring in an Interim Regulatory Affairs Director to lead and manage a large team of Regulatory Professionals. The role will be based in Berkshire.
Leads the Emerging Markets (EM) Regulatory Affairs team, including in-country Regulatory Affairs.
Is accountable for the definition of regulatory strategy and subsequent implementation, to ensure the successful registration of pharmaceutical products in EM. ...
Senior Regulatory Affairs Consultant
Company:ProClinical Ltd Location: West London Salary: 100,000+
Closing Date: 17 Jun 13
A Global Pharmaceutical Company are presently looking to bring in a Senior Regulatory Affairs Consultant to be based in their West London office
Supporting Regional Regulatory Leader to deliver assigned submissions, file or strategy for the European and International Regions. Within this plans own, and submission team, activities to ensure delivery. ...
A leading Pharmaceutical Company are looking to bring on board a Senior Consultant to join their team in Berkshire.
To manage the RA CMC activities for the product line, including currently approved products as well as next generation products. To develop and manage regulatory submission strategies, in alignment with goals and timelines established by the product brand team and project teams. ...
My client is a small biotech company specialising in natural medicine.
They are looking for a Head of Project Management to lead the project manager in the small team in Zurich.
A Leading Biotech Company are presently looking to bring in an Interim Regulatory Affairs Director to lead and manage a large team of Regulatory Professionals. The role will be based in Berkshire.
Leads the Emerging Markets (EM) Regulatory Affairs team, including in-country Regulatory Affairs
Is accountable for the definition of regulatory strategy and subsequent implementation, to ensure the successful registration of pharmaceutical products in EM. ...