An exciting opportunity has arisen for an experienced Pharmacovigilance Physician to step into a QPPV position. The role is based in London and offers the successful candidate the opportunity to become part of one of the fastest growing organisations in the world.
Head of Global Clinical Quality Assurance - European Position
I am currently working with a leading pharmaceutical company who are actively recruiting for a Senior position within their QA team. The role is Head of Clinical Quality Assurance, and requires an experienced CQA professional who can bring a wealth of professionalism and attributes to aid the company in their already impressive progress. You will need to be a 10 year+ CQA professional who can demonstrate Audit expertise, plus line management in a range of organisations.
One of the world’s leading Medical Device organisation who have been established almost 100 years with a wide variety of Medical Device products. They are a true global leader within their field and are always expanding the countries they operate in and sell the products to.
They operate in 20+ countries and have a global team of over 8,000 employees worldwide. They are now looking to expand their R&D Engineering team with an experienced Senior R&D Engineer to join this leading organisation.
Quality Engineer, Computer Systems Validation (CSV) – Zurich Region – Switzerland – upto 130,000 CHF
One of the world’s leading Medical Device organisation with a wide variety of Medical Device products. They are a true global leader within their field and are always expanding the countries they operate in and sell the products to.
They operate in 100+ countries and have a global team of over 5,000 employees worldwide. They are now looking to expand their Quality Systems Team with an experienced Quality Engineer with Computer Systems Validation experience to join this leading organisation.
My client, is currently seeking multiple Freelance Study Start-Up (SSU), home based in Sweden, on an initial 6 month contract (0.8-1.0 fte). This contract would require a start in August or Early September.
Payer/Managed Markets Senior Creative Director Needed! Qualifications:
* 3-5 years of ad agency experience in managed markets * Solid copywriting background with a portfolio to demonstrate the ability to translate scientific data and information into strategic marketing messaging and content * Acumen to write in multiple disease states and therapeutic categories * Ability to work on multiple projects and successfully interact with the team * Strong hold on the
An exciting opportunity has arisen within one of the leading company for innovative and top-quality high-tech products in the pharmaceutical industry. The group is looking for a QA Products Manager to join their team based in Frankfurt. This is an exciting opportunity for a career driven person to join a multicultural team and to take part to ambitious new projects.
Entrust Clinical People are currently resourcing for a Regulatory Affairs Senior Director for their globally renowned client. This is a fantastic time to join our client, who are currently experiencing a time of rapid development and growth. The location for this role is flexible; and can be based within Europe.
This company is a global multi-specialty pharmaceutical company headquartered in the San Francisco Bay Area. The Sr. Clinical Data Manager will provide specialized knowledge and detailed attention to lead and carry out data management data review activities in support of one or more clinical research studies.
* Defining project timelines and executing the clinical data management operations against them, and any other priorities. ...
Regulatory Affairs Manager - Sydney
Company:Real Life Sciences Location: Sydney Salary: 100,000+ Benefits: Car + Super + Bonus
Closing Date: 05 Sep 14
An exciting regulatory affairs manager role working for a growing global pharma company that have a great pipeline of new product
Contract 12 Months - Lead Data Manager - Basel, Switzerland - Leading Pharmaceutical - up to 80CHF per hour
If you would like to apply for the position or wish to learn more about the role and company please call Mark on 0044 (0) 207 255 6665 or email your CV with a brief covering note to firstname.lastname@example.org
Director of Business Analysis and Insights - International region
My client is a leading Pharmaceutical with a 12 month contract initially for a Senior Regulatory Affairs Consultant
Job Purpose • Responsible for the regulatory leadership and management of a portfolio and is the primary interface with the regulatory authorities. • Responsible for assigned non-product activities of significance to the department /company. These may be of a complex nature. ...
Clinical Statistical Programmer, Short Term Contract, Belgium
A research lead pharmaceutical client urgently require an experienced statistical programmer to come onsite and assist with a period of high work load at their Belgium site.
Clinical Programme Manager - Immuno-Oncology
Company:SEC Recruitment Location: Germany Salary: 100,000+ Benefits: Bonus, Car and Benefits Package
Closing Date: 27 Aug 14
Clinical Programme Manager - Immuno-Oncology Office Based in Southern Germany Permanent
An international pharmaceutical company currently enjoying record sales and that possess an exiting pipeline in the Immuno-Oncology field is seeking an experienced Clinical Programme Manager to join their organisation on a permanent basis. This position is office based in Southern Germany. ...
Director Quality Assurance
Company:Real Life Sciences Location: New York Salary: 100,000+ Benefits: competitive, 401K, benefits package
Closing Date: 17 Sep 14
This position is responsible for overseeing the Quality Assurance function for the Cardiovascular Research centre and the Clinical Trials Center. Direct reports include Quality Assurance Manager and Quality Assurance Associate. Responsibilities include interviewing, hiring, and training employees; planning, assigning, and directing work; appraising performance, rewarding and disciplining employees; addressing complaints and resolving issues.
Category: Clinical Development Type: Pharmaceutical / Biotechnology Therapeutic Area: Oncology
Medical Director - Belgium
Company:RBW Consulting Location: Brussels Salary: 100,000+ Benefits: Full Package
Closing Date: 05 Sep 14
Seeking Medical Director with strong leadership skills to manage Medical Affairs function of this leading company.
Essential requirements include a Medical degree and fluency in French, Dutch and English.
Role covers Medico-marketing, Pharmacovigilance, Regulatory and Market Access.
Strong focus is on personality - the ability to lead, mentor and coach is a top priority
New contract available immediately for a consultant with demonstrable experience of advertising and promotional materials for the healthcare sector within a regulatory frame. This opportunity is based on our client’s site in Oxfordshire (scope for partial home working).
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