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QA Specialist - 6 month Fixed Term Contract. Job

Company: Celgene Ltd
Location: Hillingdon, England, United Kingdom
Salary: On Application
Closing Date: 21 Apr 15More Details
Position Specialist, QA
Supervisor Associate Director, Quality Compliance – Celgene Europe
Prerequisites BS (or equivalent) in a technical of scientific discipline.

Demonstrated pharmaceutical (or other related industry) quality experience. ...

Associate Director, EMEA International Regulatory Affairs - Based in UK or Switzerland. Job

Company: Celgene Ltd
Location: Hillingdon, England, United Kingdom
Salary: On Application
Closing Date: 21 Apr 15More Details
...

Associate Director Regulatory Afffairs - Contract Job

Company: Celgene Ltd
Location: Hillingdon, England, United Kingdom
Salary: On Application
Closing Date: 21 Apr 15More Details
Purpose

• Demonstrably the affiliate expert in quality and regulatory, acting as the primary point of contact for all affiliate quality and regulatory issues. ...

Director Partnership, Middle East Africa Job

Company: Celgene Ltd
Location: Middlesex, England, United Kingdom
Salary: On Application
Closing Date: 21 Apr 15More Details
Responsibilities will include, but are not limited to, the following:

• Strategy development and execution
o Brings an innovative mindset to our mission to improve patient access in the region
o Uses expertise to develop innovative options to geographical expansion in the region
• Relationship management
o Responsible for the development of an open, transparent and trusting relationship with key partner contacts and internal stakeholders. ...

Senior Manager EMEA Regulatory Policy & Intelligence Job

Company: Celgene Ltd
Location: Hillingdon, England, United Kingdom
Salary: On Application
Closing Date: 21 Apr 15More Details
POSITION Senior Manager EMEA Regulatory Policy & Intelligence
SUPERVISOR Director Regulatory Policy & Intelligence
DEPARTMENT EMEA Regulatory Affairs
PREREQUISITES Understanding of IT tools and information systems
Understanding of EU regulatory legislation and guidance required. Scientific discipline degree required; Extensive pharmaceutical industry or health authority experience, with recent experience in regulatory intelligence preferred.. ...

Key Account Manager, London - Oncology Job

Company: Celgene Ltd
Location: Windsor, England, United Kingdom
Salary: On Application
Closing Date: 21 Apr 15More Details
Role and Responsibilities:
• Exceeding UK/Ireland Territory Sales Targets for promoted brands
• Analyse the issues, priorities and funding processes related to funding of cancer treatment in the NHS and translate into opportunities for the Celgene product portfolio and joint customer agendas.
• Ensuring local implementation of guidelines and pull through of secured funding for promoted brands. ...

Director, Human Resources, UK & Ireland Job

Company: Celgene Ltd
Location: Hillingdon, England, United Kingdom
Salary: On Application
Closing Date: 21 Apr 15More Details
Celgene is a global biopharmaceutical company leading the way in medical innovation to help patients live longer, better lives. Our purpose as a company is to discover and develop therapies that will change the course of human health. We value our passion for patients, quest for innovation, spirit of independence and love of challenge. ...

Regional Medical Liason - Lymphoma - South Job

Company: Celgene Ltd
Location: Hillingdon, England, United Kingdom
Salary: On Application
Closing Date: 21 Apr 15More Details
...

Regional Medical Liaison, Lymphoma - North Job

Company: Celgene Ltd
Location: Windsor, England, United Kingdom
Salary: On Application
Closing Date: 21 Apr 15More Details
...

Manager, Regulatory CMC International Job

Company: Celgene Ltd
Location: Hillingdon, England, United Kingdom
Salary: On Application
Closing Date: 21 Apr 15More Details
POSITION Manager, Regulatory CMC International
SUPERVISOR Senior Manager, Regulatory CMC
DEPARTMENT Technical Operations
PREREQUISITES BS/BA degree in Scientific Discipline (Masters or higher preferred) with extensive experience in the pharmaceutical industry or in CRO, including specialist CMC regulatory experience.

Responsibilities will include, but are not limited to, the following:

1. ...

Clinical Research Assistant II Job

Company: Celgene Ltd
Location: Hillingdon, England, United Kingdom
Salary: On Application
Closing Date: 21 Apr 15More Details
Manage Investigative Site activities to ensure that subject safety is protected and that timely high quality data are collected in compliance with regulations

Responsibilities include, but are not limited to:

1. ...

Senior Manager QA Job

Company: Celgene Ltd
Location: Hillingdon, England, United Kingdom
Salary: On Application
Closing Date: 21 Apr 15More Details
Senior Manager, Quality Assurance – Qualified Person

Celgene is a global biopharmaceutical company leading the way in medical innovation to help patients live longer, better lives. Our purpose as a company is to discover and develop therapies that will change the course of human health. We value our passion for patients, quest for innovation, spirit of independence and love of challenge. ...

Associate Director, Global Clinical Site Contracts Job

Company: Celgene Ltd
Location: MARIN, Switzerland
Salary: On Application
Closing Date: 21 Apr 15More Details
Celgene is a global biopharmaceutical company leading the way in medical innovation to help patients live longer, better lives. Our purpose as a company is to discover and develop therapies that will change the course of human health. We value our passion for patients, quest for innovation, spirit of independence and love of challenge. ...

Senior Associate, Clinical Trials (2 year maximum duration contract) Job

Company: Celgene Ltd
Location: MARIN, Switzerland
Salary: On Application
Closing Date: 21 Apr 15More Details
Celgene is a global biopharmaceutical company leading the way in medical innovation to help patients live longer, better lives. Our purpose as a company is to discover and develop therapies that will change the course of human health. We value our passion for patients, quest for innovation, spirit of independence and love of challenge. ...

Senior Manager, Clinical Studies Management Job

Company: Celgene Ltd
Location: MARIN, Switzerland
Salary: On Application
Closing Date: 21 Apr 15More Details
Celgene is a global biopharmaceutical company leading the way in medical innovation to help patients live longer, better lives. Our purpose as a company is to discover and develop therapies that will change the course of human health. We value our passion for patients, quest for innovation, spirit of independence and love of challenge. ...

VP Regulatory Affairs - Consulting

Company: Morgan Prestwich Pharmaceutical Recruitment
Location: UK. South East
Salary: Negotiable
Benefits: Competitive Salary, Benefits Package
Closing Date: 19 May 15More Details
This is a new position due to the growth of my client. They are looking for an experienced Regulatory candidate to Lead their European team. The right level of candidate will be a Director / Senior Director / Vice President Regulatory Affairs. You will be well connected within the industry, coupled with a strong background of advising clients and delivering high calibre project work.

NON-Clinical Senior Project Manager / Director

Company: Morgan Prestwich Pharmaceutical Recruitment
Location: UK - England - South - South East
Salary: Negotiable
Benefits: Full benefits package
Closing Date: 19 May 15More Details
Due to department expansion, my pharmaceutical client are looking for an experienced Non-Clinical Senior Project Manager or Director to join their team in the south of England. The Non-Clinical Senior Clinical Project Manager or Director will be tasked with global Non-clinical projects. My client are looking for candidates with a strong development background, who can work within a team environment.

Clinical Project Manager (CPM) or Senior Clinical Project Manager (SCPM) - Late Phase

Company: Morgan Prestwich Pharmaceutical Recruitment
Location: Any European location - Home or Office based
Salary: Negotiable
Benefits: Full benefits package with bonus & car allowance
Closing Date: 19 May 15More Details
Newly created position for a Late Phase Clinical Project Manager to focus on European Trials. I am looking for a home or office based Late Phase Clinical Project Manager (CPM, (peri, post approval, Real World Evidence, RWE) to be based in any European Country, preferred is UK. Reporting into the European Head of Project Management, the CPM or SCPM will be tasked with high calibre project delivery.

Hospital Sales Specialist - London/Essex

Company: Roche
Salary: On Application
Closing Date: 20 Apr 15More Details
We are seeking a Hospital Sales Specialists to maximize sales cost-effectively within a defined set of accounts enabling Roche to maintain and further develop its Pharma turnover. Reporting to the Sales Manager you will be responsible for the delivery of sales in line with company targets maximising Roche's interests and promoting patient care across London and Essex. ...

Resourcing & Reporting Lead

Company: Roche
Salary: On Application
Closing Date: 20 Apr 15More Details
This opportunity can be based in either Welwyn Garden City or Basel. The Resourcing & Reporting Lead manages the audit programme & resource management process which encompasses the planning, scheduling, resourcing and delivery tracking of audits in alignment with strategic requirements established by the PDQA Strategy Heads. This role maintains a suite of reports that support communication of the PDQA Audit Programme and associated resourcing to internal and external stakeholders. ...

Senior/Executive Medical Director/Vice President - Oncology-120961

Company: PPD
Salary: On Application
Closing Date: 21 Apr 15More Details

We are seeking someone to join our Global Product Development team in the field of Oncology.

The Global Product Development group, a part of the medical organisation, is comprised of experienced drug development professionals who provide medical, scientific and product development expertise to our clients, internal PPD clinical operations and business development teams. ...

Rewards Specialist-122701

Company: PPD
Salary: On Application
Closing Date: 21 Apr 15More Details

PPD is a leading global contract research organization providing drug discovery, development and lifecycle management services. Our clients and partners include pharmaceutical, biotechnology, medical device, and academic and government organizations.



PPD are currently recruiting for a Reward Specialist in our EMEA head office based in Cambridge to work as part of the global reward team covering the UK and Ireland. ...

Medical Information Associate - German Speaking-122702

Company: PPD
Salary: On Application
Closing Date: 21 Apr 15More Details

Due to continued success and growth, PPD is currently looking to recruit a German Speaking Medical Information Associate to be based in our EMEA Headquarters in Cambridge, UK. The role of Medical Information Associate works within our Medical Communications team to provide technical and medical information in response to enquiries received via phone, email, internet or mail. These enquiries may come from consumers and health care professionals. ...

cGMP Compliance Assessor - QA - 12 Month contract - UK

Company: MSI Pharma
Location: Buckinghamshire
Salary: On Application
Benefits: Hourly Rate: £35-42
Closing Date: 17 May 15More Details
A market leading Pharmaceutical company are looking for a cGMP Compliance Assessor to join their project on an initial 12 month contract basis.

Medical Dictionary Analyst

Company: Chiltern International
Location: Home based Anywhere in UK
Salary: On Application
Closing Date: 17 May 15More Details
Medical Dictionary Analyst required for 6 month contract with global pharma, home based role anywhere in UK

Real-world Data (RWD) Scientists

Company: Roche
Salary: On Application
Closing Date: 20 Apr 15More Details
As a RWD Scientist, you will partner with other scientists and functional leads in the design and execution of RWD strategy and delivery in one or more therapeutic areas across phases of drug development. Solid drug development understanding, expertise in RWD strategic applications, RWD analytic methodological approaches as well as effective communication skills are required. ...

Strategic Alliance Leader

Company: Roche
Salary: On Application
Closing Date: 20 Apr 15More Details
Engage with partners on collaborations that drive the long-term strategy and direction of Real World Data-S (RWD-S).  Liaise with internal stakeholders on RWD-S support to meet business requirements. Identify and evaluate future opportunities and collaborations in RWD.  Develop and cultivates partnership with internal and external stakeholders. Responsibilities Functional Area Liaise with internal stakeholders (e.g. ...

Real World Data-Science Methodology Specialist

Company: Roche
Salary: On Application
Closing Date: 20 Apr 15More Details
Expert in methodologies used in RWD strategy, study design and analyses. Provide relevant expert support and consulting to RWD-S and other partners in PD, GMA, GPMA and affiliates. Expertise typically includes statistical methodologies, benefit risks, comparative effectiveness, health economics, outcome research, etc. ...

Real World Data-Science Methodology Specialist

Company: Roche
Salary: On Application
Closing Date: 20 Apr 15More Details
Expert in methodologies used in RWD strategy, study design and analyses. Provide relevant expert support and consulting to RWD-S and other partners in PD, GMA, GPMA and affiliates. Expertise typically includes statistical methodologies, benefit risks, comparative effectiveness, health economics, outcome research, etc. ...

Scientific & Methodology Expert - Infectious Disease

Company: Roche
Salary: On Application
Closing Date: 20 Apr 15More Details
Summary: The candidate will be the primary interface between the pRED Clinical Development organization and the Infectious Disease Therapeutic Area (ID DTA). He/she will lead strategic discussions on clinical development plans. In this critical role, he/she will apply expert ID medical and early clinical development knowledge, as well as operational perspectives on executing clinical development plans for assets within the portfolio. ...
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