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 - BIOSIMILARS!!
Company:Key People Limited Location: Berkshire Salary: 100,000+ Benefits: Significant bonus and benefits
Closing Date: 24 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.
My client is keen to find an experienced Pharmaceutical Physician with a commercial background in Pharmacovigilance / Drug Safety to work on a permanent basis in London however due to the Global operations of the company the position could also be based in Germany, Rotterdam or Milan.
Head of Regulatory Affairs – European Experience
Freelance QM/GMP Consultant gesucht fĂĽr unseren Kunden, ein pharmazeutisches Unternehmen mit Sitz in Bayern, ab sofort und fĂĽr 6 Monate.
Senior Quality Engineer
Company:Real Staffing Location: Lawrence Salary: 100,000+
Closing Date: 14 Jun 13
Working in a growing and innovative medical device company, you will be working among a team of Quality Engineers. In the Senior Quality Engineering role you will be developing quality systems and ensuring compliance with ISO standards. The Senior Quality Engineer will also be conducting audits for evaluation of supplier compliance and conducting internal audits. ...
I am looking for VP level in Health economics, Epidemiology and Market Access
Head of Clinical Research - Portugal
Company:RBW Consulting Location: Portugal Salary: 100,000+ Benefits: Relocation and benefits
Closing Date: 17 Jun 13
Exciting opening for very experienced Clinical Research Physician who has managed Phase I to IV Clinical Trials, has extensive employee management experience and experience in Neruoscience would be desirable.
Recruiting for a Medical Science Liaison to join a company in the pharmaceutical industry in a permanent role in the North and South.
As Medical Science Liaison you will be involved providing field-based non-promotional scientific and/or educational support for the UK Oncology business.
CMC Expert, Range of Therapy Areas, English Speaking, Variation between QA and Regulatory Departments, Zug
Become the CMC expert/ go to person for CMC for an upcoming start up company with a number of established products on the market. The role will be focused on submissions and writing for CMC for the FDA. Due to this being a smaller company your duties will be broad from mentoring junior staff to coverage of change control, aspects in QA and working closely with supply chain.
This is a fantastic opportunity to work in a leading biologics department at the heart of a global pharmaceutical company. In this position you will have a significant role in the preparation and submission of documents from early development to post approval in CMC. In addition to this, there is a strong emphasis on international submissions.
Seeking Senior/Principal QE for CALIFORNIA medical device co!
Company:Real Staffing Location: Minneapolis Salary: 100,000+ Benefits: depending on experience
Great 6 months contract role - Franchise Operational QA Manager in Basel, Switzerland in an international pahrmaceutical company specialized in prescription drugs. Main requirements:Ten (10) plus years of experience in clinical requirement: development and the pharmaceutical industry preferably with at least 3 years in Quality Assurance/ Compliance roles.
Project manager for Croatian based role for an international CRO. They are starting two Phase III Cancer studies and require a Project Manager to join their team. The successful Project Manager must have strong experience in Project Management. This is more important that having experience of Oncology studies. Ideally this would be for 1.0 FTE. ...
Late Phase Freelance Clinical Research Associate (CRA) - CRO - Germany
Late Phase Freelance Clinical Research Associate (CRA) - CRO - Germany
CRA required for German based role for an international CRO. They are starting two Phase III Cancer studies and require a CRA with strong late phase experience to join their team. The successful CRA must have strong experience in close outs, feasibilities etc. ...
I have been employed by a rapidly developing and well respected pharmaceutical company based in New York State, USA! They are seeking GCP and Senior GCP Auditors to join their expanding Quality Assurance division. This role can either be Office Based or Home Based. If you are looking for an organisation that is renowned for their scientific excellence in the research and development of pharmaceuticals, then please get in touch!!
I am currently recruiting for a Medical Services Manager role for an initial 3 month contract role based in Berkshire. This involves being direct management for the Med Info/Med Affairs department and also the Pharmacovigilance departments. ...
Small Pharmaceutical company is seeking a talented Contract Clinical Data Manager to join the Clinical team for a 6 month (extendable contract). The Clinical Data Manager is responsible for overseeing data management tasks from study start-up through database lock, for development programs. This individual will be a point of contact with CROs and other external vendors for all issues related to data management.
Associate Director of forecasting and Strategy - Switzerland
* Support the implementation of the standardized procedures, processes and systems for CAPA * Deliver education and interactive training for CAPA users to deliver consistent compliant CAPAs including Failure Investigation, CAPA Review Board and CAPA content * Assist CAPA users with development and documentation of problem statements, containment and correction, root cause, and action plan (including effectiveness monitoring) determination.
My Client is a new international pharmaceutical company based in Switzerland in the Zurich Area.
They are looking for someone to join their growing Clinical team as a Clinical Operations Manager.
Senior Regulatory Affairs Specialist-Market Leading Devices
A great opportunity has arisen in the medical device industry for a Senior Regulatory Affairs Specialist. Through this role, you will gain the fantastic opportunity to work with market leading products. You will be working a range of innovative products, from Class I through to Class III high risk products. Through this you will gain invaluable experience and strengthen your skills in regulatory affairs.
Patient Safety Physician Contract
Company:SEC Recruitment Location: North West England Salary: 100,000+
Closing Date: 06 Jun 13
A leading Pharmaceutical company currently has an urgent requirement for a Patient Safety Physician to join their Translational Patient Safety Group on a rolling 6 month freelance contract basis.
Within this assignment you will use your medical expertise to enable high-quality and timely proactive safety evaluation of emerging data from various sources while also developing a safety strategy for a candidate product. ...
An opportunity has arisen to join the Senior Leadership Team within a leading pharmaceutical organization at a key time. This position is very broad and offers the prospect to make an impact at both a regional and global level. The ideal candidate will be considered the therapy area expert in the rapidly changing and complex global access and reimbursement environment.
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?
Senior Medical Expert Dermatologist South France - up to €120,000
Company:Barrington James Clinical Location: uk, Germany, France, Spain, Switzerland, Italy Salary: 100,000+
Closing Date: 16 Jun 13
My client is an innovative, leading Pharma currently searching for an experienced medical professional to join them as Dermatology Medical Expert for their expanding team. This is a key role in their plans for future expansion across Europe and so the company is keen to attract a high calibre, motivated Medical Doctor looking for an exciting, diverse role.
Medical Expert Dermatologist South France - beach location, Pharma, super package, 6 figures
Company:Barrington James Clinical Location: uk, Germany, France, Spain, Switzerland, Italy Salary: 100,000+
Closing Date: 16 Jun 13
My client is an innovative, leading Pharma currently searching for an experienced medical professional to join them as Dermatology Medical Expert for their expanding team. This is a key role in their plans for future expansion across Europe and so the company is keen to attract a high calibre, motivated Medical Doctor looking for an exciting, diverse role.
VP Medical Affairs Oncology Europe up to €200,000 + Package
Company:Barrington James Clinical Location: uk, Germany, France, Spain, Switzerland, Italy Salary: 100,000+
Closing Date: 16 Jun 13
JOB SUMMARY
Top 10 pharma company with an excellent pipeline in oncology. This role will lead the pre-launch and launch activities for these developments across Europe including some emerging markets.
MEDICAL PROJECT MANAGER ONCOLOGY - MUNICH €100,000