Home-based Biostatistician - Contract - 6 months, Global CRO, £55/hour+
A global CRO, based in the UK are currently seeking for an experienced Biostatistician to join them for a rolling 6 month contract. You can either be office based or fully home-based depending on your location and preference.
This is a great opportunity to be working for one of the leading CROs within the industry. Do get in touch should you be interested.
Statistical Consultant, Long Term Contract, Germany
SEC Pharma is proud to working on behalf of an industry renowned pharmaceutical company. This is a very rare and exciting opportunity for a statistical consultant to join an innovative and forward thinking company on a very long term contract. A 24 month contract is on offer along with a very competitive hourly rate.
In summary, your role as a statistical consultant will be to provide statistical and programming support to the project statisticians in the group.
Job Title: Medical Science Liaison Manager Location: Home Based East Coast...
Head of Market Access within Biosimilars - covering Europe
Company:ProClinical Ltd Location: Switzerland Salary: 100,000+ Benefits: + bonus + car allowance + medical cover
Closing Date: 16 Sep 14
Here is an opportunity to be responsible for defining and implementing the Market Access, Contracting and Tendering strategies for one of the industry’s most exciting companies.
Having experienced monumental success over the last 18 months, they are creating a new franchise within the Biosimilar market. In this position, you will be responsible for maximising market penetration of assets and for protecting overall profitability and long-term sustainability of the business. ...
Associate Director, Clinical Study Management Cambridgeshire, South East England Freelance, 6-12 Month Contract
A multi-national pharmaceutical company currently carrying out a pan-European recruitment drive across the business following strong financial results is seeking an Associate Director, Clinical Study Management to join their study management group within the UK, focused on the delivery and submission of a Phase II/III clinical programme. ...
Head of Regulatory Affairs – Global Consumer Healthcare Company – South East
Company:Meet Salary: 100,000+ Benefits: For full details of the fantastic benefits that come with this offer please email email@example.com
Closing Date: 18 Sep 14
My client is looking for an experienced regulatory affairs professional to head up their Regulatory team in the South East. With a fantastic product portfolio this a great time join a rapidly growing company who can offer a wide range of responsibilities and the opportunity to make a indelible mark on the client’s direction and progress.
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.
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
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
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. ...
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
PharmiWeb.com is Europe's leading industry-sponsored portal for the Pharmaceutical sector, providing the latest jobs, news, features and events listings.
The information provided on PharmiWeb.com is designed to support, not replace, the relationship that exists between a patient/site visitor and his/her