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The latest Executive Pharmaceutical Jobs jobs - BETA

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Regulatory Affairs Director - New Jersey
New Jersey
Feb 27
Director, Regulatory Affairs This an exciting opportunity to join a clinical stage biopharmaceutical company focused on the development and commercialization of targeted antiviral therapies. The...
Regulatory Lead Pediatrics – global pharma company with HQ in West Germany – up to 130,000 € plus relocation - 3 days HB
Germany
Feb 27
Do you want to be in the front row fighting cancer on children, which is still number one cause of death by disease? Then this is the right opportunity for you! We are looking for an experienced Regulatory Affairs Manager, who wants to use his knowledge about pediatrics in one of the biggest pharmaceutical organizations worldwide. You can expect an open environment, life-changing projects and excellent benefits.
Contract Qualified Person
Groningen
Feb 27
Qualified Person QP (FTC) – Groningen – up to €800 per day Optimus Life Sciences is working with a multinational Pharmaceutical company to find a Qualified Person.Reporting to the Head of Quality, you will be working alongside 5 other Qualified Persons who can assist you during your training period. Your primary responsibility will be to support the batch release of large volume sterile products. Tasks: * Implement QP release of sterile product(s) to market. ...
Product Classification Lead
Middlesex
Feb 27
Product Classification Lead - Earn up to £417 per day plus benefits (PAYE) or £540 per day (LTD)We are recruiting for a Product Classification Lead to join their team in Middlesex and lead the global export product classification data cleanse and build the service processes for ongoing management of product classification (ECN codes, Drug Precuror, US content determination and other export control classifications)
Consultant Senior Statistical Programmer - Switzerland
Switzerland
Feb 27
A prestigious Pharma in Switzerland are actively looking to add a talented senior statistical programmer to their established biometrics team.As a statistical programmer you will be involved in providing expert programming support to the biometrics functions across several key studies. You will be fully supported in your role by the wider team where you will be working very closely with the senior members.
Global Medical Director
United Kingdom
Feb 27
Global Medical DirectorA top 10 pharma company is seeking to add to its senior leadership team through the addition of a new global medical...
Senior Medical Director
North Carolina
Feb 24
Job Summary:  Forward Thinking Medical Communication agency looking to bring in a Senior Medical Director to produce scientific content in various therapeutic categories. As...
Senior Manager, Quality Control
Cincinnati
Feb 24
Senior Quality Control Manager needed for rapidly expanding Top-Tier Pharmaceutical FirmSenior Manager | Quality Control | Small Molecule | GMPGreater Cincinnati Area | Ohio$80,000 - $140,000 + bonus +...
Biostatistician Needed for Expanding Biotech Company
Texas
Feb 24
Biostatistician, Needed for Expanding Biotech CompanyBiostats | Phase I-IV Clinical TrialsGreater North East Area, Remote$120,000 - $140,000 +complete benefits package  An expanding medical device...
Medical Scientific Liaison - Immunology
Austria
Feb 24
We are currently seeking dynamic individuals for a Medical Scientific Liaison position with a top global pharmaceutical organisation. The MSL will act as a representative...
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Senior Clinical Research Specialist – NL/BE borders
Netherlands
Feb 24
Senior Clinical Research Specialist/Project Manager – Netherlands CRA, Field Research, Senior Clinical Research, Regulatory Standards, Follow up Studies, Oncology, SOPs, Monitoring, Cardio, Project manager, Study, Trial My client a busy, biotech in the Netherlands require a Senior Research Specialist/Project Manager. Someone with good CRA, documentation, monitoring and all round Project management. The successful candidate will be: - Proactive, patient, flexible and dynamic. ...
Regulatory Affairs Director - UK
Homebased UK
Feb 24
My client is looking to strengthen their Regulatory Consulting team in Europe and are seeking a Director, Regulatory Strategy to join their Global Consulting group. I am keen to engage with highly strategic individuals ideally with a senior background in CRO's.
Toxicologist - Netherlands
Netherlands
Feb 24
Toxicologist – Netherlands (6 to 12 months freelance) Toxicologist, Project Manager, Scientist, Regulatory services, subject matter expert, engagement, stakeholder management, public health, requirements. This is a 6 to 12 months assignment for a talented and experienced Toxicologist/Scientist with good engagement and stakeholder management skills. ...
Senior QA Specialist (12-month Contract)
Republic of Ireland
Feb 24
Senior Quality Assurance Specialist – Republic of Ireland (12-month contract)Up to £100/hourOptimus Life Sciences is working with a multinational bio-pharmaceutical client to find a Quality Assurance Specialist. You will be responsible for carrying out tasks and projects in the clinical division and required to provide support with biologic IMPs.You will receive the opportunity to lead the QA team, consisting of 5 other officers. ...
Head Global GCLVP QA (Good Clinical, Laboratory and Pharmacovigilance Practices) (f/m)
Aachen
Feb 24
Recruiting, coaching and developing personnel and managing resources, assisting the Head of Global Quality Assurance in strategic definition and planning paired with ensuring planning, preparation and performance of internal and external system audits for GCP, GLP and GVP against company standards, SOPs and applicable international regulations and guidelines
Global Market Access-3-4 months contract-Swiss
Switzerland
Feb 23
Global Market Access-3-4 months contract-SwissFor one of our biggest client we are currently looking for a Marker Access ContractorThe role involves:Implementation of market access strategy, managing Global affiliates, creating resources, literature review, communicate with material with local team. You will be working with the respective countries helping them adapt strategies to the local market.
QA engineer medical devices
Zwolle
Feb 23
For an interim assignment for 6 months, we are now urgently looking for a Quality specialist for one of the most exciting Medical Device companies in Europe. Based in the North of the Netherlands, they are looking for someone with medior to senior level of experience in QA and/or validation within the Med Dev industry.
QA customer complaints specialist
Breda
Feb 23
Amoria Bond is currently working on an exciting opportunity for an experienced QA Specialist. The project will take 12 months and you will be working in Breda (South of Netherlands) at one of the market leading companies in the Pharmaceutical industry.
Health Economics Modeling Consultant - Major Biotech
London
Feb 23
A renowned Biotech in the South East of England are actively looking for a very talented and experienced Health Economics Modeler to provide expert, ongoing consultative support to their in house modelling centre of excellence. Initially offered on a 2 year contract this will be office based in their stunning UK offices. Very competitive hourly rate offered - please feel free to contact me at any time to discuss this in more detail.
Contract Statistical Programmer - Switzerland
Switzerland
Feb 23
A prestigious Pharma in Switzerland are actively looking to add a talented contract statistical programmer to their SAS programming team.As a statistical programmer you will be involved in providing expert programming support to the biometrics functions across several key studies. You will be fully supported in your role by the wider team where you will be working very closely with the senior members.
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Medical Science Liaison
Switzerland
Feb 23
Exciting Opportunity Top BiotechAs a leading global biotech our client has one of the most solid yet innovative product pipelines in the industry today.   ...
Senior Medical Director
Chicago
Feb 23
Job Summary:  Rapidly growing Medical Communication agency seeking a full-time Senior Medical Director to deliver scientific services and products in various therapeutic categories.  As...
Executive Director of Regulatory Affairs.
England
Feb 22
The consultant running this executive search is Sam Murphy. For more information or to apply to the position please contact Sam via email – sam.murphy@tecgroup.net
( Senior ) Director, Business Development - Sweden
Sweden
Feb 22
Radek Weichert at Skills Alliance is supporting a stable and highly regarded Contract Research Organisation in their search for a driven Business Development (Senior) Director....
Senior Product Manager (Medical Device)
Durham
Feb 22
Multi-Million Dollar Medical Device CompanyLocation: North CarolinaCompensation: $110k – 130k + bonus + benefitsOur client, a multi-million dollar medical device company, is looking for...
QA / RA Consultant
Eindhoven
Feb 22
Job descriptionWorking within a Global streamlining project of the Quality system my client is searching for a professional within expertise in regards to regulations...
Vice President, Healthcare Policy
Washington Navy Yard
Feb 21
Our client, a leading healthcare consulting firm, is looking to bring on a VP of Policy to manage, design, and conduct quantitative analyses on health...
Sales Training (Pharmaco Experience Only)
New Jersey
Feb 21
Sales Training – Leading Pharmaceutical CompanyMarketing, Sales, Development$140,000 - $170,000 + bonus + competitive benefits package My client, a leading pharmaceutical firm, is currently looking for...
Sr. to Principal Clinical Programmer Needed
San Francisco
Feb 21
Sr. to Principal Clinical Programmer Needed for Expanding Biotech CompanySAS | Phase I-IV Clinical Trials | R CodingUSA, California$120,000 - $160,000 +complete benefits package (B.O.E.)...
BD Director Respactable CRO - Italy
Italy
Feb 21
Radek Weichert at Skills Alliance is supporting a stable and highly regarded Contract Research Organisation in their search for a driven Business Development (Senior) Director....
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BD Director Respectable CRO - Spain
Spain
Feb 21
( Senior ) Director, Business Development – Spain Radek Weichert at Skills Alliance is supporting a stable and highly regarded Contract Research Organisation in their search for...
Quality Lead - Dublin - 12 Months
Dublin
Feb 21
Quality Verification LeadLocation: Dublin, IrelandContract length: 12 Months12 Month Contract – Quality Lead – Dublin - €65-75/hourOptimus Life Sciences are working with a Global Biotech Company based in Dublin, Ireland and together we are looking Quality Lead for a fast-paced project. This project will last a minimum of 12 months initially. The proposed started date is Mid-March but can be flexible, interviews will take place as early as next week. ...
Medical Consultant - Research and Development
Germany
Feb 21
We are working with one of the largest global pharmaceutical organisations in the world as they grow out their consulting teams within Germany. With a...
Senior Medical Consultant
Berlin
Feb 21
We are currently working with a rapidly growing global consultancy with offices across Europe and the US and a core focus on both the Pharmaceutical...
Medical Advisor - Immunology
Munich
Feb 21
We are currently working with one of the world`s leading global pharmaceutical organisations as they expand out their Medical Affairs teams in the field of...
Associate / Director, Drug Safety and Pharmacovigilance Operations
North Carolina
Feb 21
Associate / Director, Drug Safety and Pharmacovigilance Operations Associate / Director, Drug Safety and Pharmacovigilance Operations North Carolina $130,000 - $160,000 + excellent bonus + excellent benefits
Diagnostics Sales Director-Change Management-CH
Zürich
Feb 21
You will be responsible for managing and leading a team of both fresh and seasoned sales & marketing professionals within the diagnostics market. Other responsibilities will including bringing harmonisation within the team following a recent merger, as well as working closely with customers and helping to define the global strategy.
Senior Manager, Global Med Info (Onc/Vir) - W.Euro
Europe
Feb 21
Julia Day is looking for two Senior Managers, Medical Information to take responsibility for oncology and/or virology within a Global Medical Information team. The roles...
Market Access Director DACH
Munich
Feb 21
Our client is a young and dynamic start-up Biopharma with an immensely exciting pipeline of products set for launch in the US and Europe. As...
Health Technology Assessment (HTA) and Outcomes Research Senior Manager
Zürich
Feb 21
Our client is a young and dynamic start-up Biopharma with an immensely exciting pipeline of products set for launch in the US and Europe. As...
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Regulatory Consultant-MDR Change Project-Medical Devices-Bern
Bern
Feb 20
Regulatory Consultant-MDR Change Project-Medical Devices-Bern, SwitzerlandStart date: As soon as possibleHourly Rate: dependant on experience but around 90-100CHF an hourLocation: Bern AreaHours: Part Time, leading up to full time during audit times.NonStop Medical Devices have been enlisted with an urgent contract for a regulatory affairs and quality assurance consultant. If you are available with short notice and have directly worked on the MDR changes, we want to hear from you today. ...
PHARMA CONTRACT - Head of Quality Operations - Greater London
Slough
Feb 20
NonStop Pharma is working with a growing biologics company who are focused on creating innovative products for the biopharma market. They are actively looking for a talented individual to act as interim head of quality. ...
Regulatory Manager (CMC) - 12 Month Contract
Middlesex
Feb 20
i-Pharm Consulting are recruiting for…ROLERegulatory Manager (CMC)LOCATION: Middlesex RATE: £60-£65 per hour ROLE: Leading Biotech are seeking a Regulatory Manager to assist in CMC activities.The focus will be on Oncology products and tasks will focus on CMC components of development and maintenance filings. There may also be a need to utilise CMC experience for change control and gap analysis amongst other activities. ...
Regulatory Manager (CMC) - 12 Month Contract
Cambridge
Feb 20
i-Pharm Consulting are recruiting for…ROLERegulatory Manager (CMC)LOCATION: Cambridge RATE: £60-£65 per hour ROLE: Leading Biotech are seeking a Regulatory Manager to assist in CMC activities.The focus will be on Oncology products and tasks will focus on CMC components of development and maintenance filings. There may also be a need to utilise CMC experience for change control and gap analysis amongst other activities. ...
Senior Regulatory Manager (12 Month Contract)
Cambridge
Feb 20
i-Pharm Consulting are recruiting for…ROLESenior Regulatory Manager LOCATION: Cambridge RATE: £60-£70 per hour ROLE: Leading Biotech are seeking a Senior Regulatory Manager to work within their EU team and assist on a range of activities.The focus will be on Oncology products and tasks will primarily focus on maintenance and development of key product portfolio. ...
Interim Senior Scientist PK/PD - NRW - 6+ Months (m/w)
Nordrhein-Westfalen
Feb 20
Interim Senior Scientist PK/PD - NRW - 6+ Months (m/w)I am urgently looking for an interim professional to support the Non-Clinical Pharmacokinetic department of one of my clients, an international pharmaceutical company, at their side in central NRW. The initial contract is scheduled to last at least 6 months with a high possibility of extension. The aspired start date would be 1. March of 2017, which is why interviews will be conducted later this week. ...
Non-Clinical biostatistician - 6 month - Freelance
Belgium
Feb 20
MSI Pharma is working with a globally recognised healthcare company in Belgium to recruit a Non-Clinical biostatistician for a 6 month assignment.
Senior Quality Control Manager
Cork
Feb 18
Senior Quality Control Manager The Company My client is the world leader in delivering therapeutics that provide meaningful advances to patients who live with serious...
Account Director
Germany
Feb 17
ACCOUNT DIRECTORGERMANY OR SWITZERLAND (Home office)One of Worlds largest CROsMy client, a world leading CRO is currently recruiting an Account Director to manage their top 2-3 Accounts.
Senior Medical Director - Medical Communications
New York
Feb 17
Forward Thinking Medical Communication agency seeking full-time Senior Medical Director to produce key scientific content in a variety of therapeutic categories. As the Senior Medical  ...
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Urgent: Medical Technology Manager-Munich (m/w)
München
Feb 16
Urgent: Medical Technology Manager - Munich area - 3-6 months (m/w)I am currently looking for an experienced Project Manager to join a Medical Technology Company in the Munich area. As they are looking to hire someone before the 1. of March, interviews will be conducted early next week. The contract is initially scheduled for 3-6 months, with the intention of being extended on a permanent basis afterwards. ...
Senior Clinical Research Specialist - NL/BE Borders
Netherlands
Feb 16
Senior Clinical Research Specialist – NL/BE borders CRA, Field Research, Senior Clinical Research, Regulatory Standards, Follow up Studies, Marketing, Market development, Lab work, Testing, Cathlab, Coronary, Renal, Cardio Global brand is keen to add an experienced Lab focused Senior Research Specialist. Someone with good CRA, Lab and marketing related experience. You will play a key role in supporting field activities for studies in this area. ...
CRA role with Medical Device company
New York
Feb 16
We are seeking a CRA Role With Medical Device Startup! You will be responsible for monitoring activities across numerous sites on the East Coast.Qualifications:...
Director, Regulatory Affairs Advertising and Promotion
New Jersey
Feb 15
A global specialty pharmaceutical company in New Jersey is currently seeking a Director, Regulatory Affairs Advertising and Promotion to provide strategic guidance for the review...
Medical Director - UK and Ireland
Scotland
Feb 15
Medical Director - UK & Ireland Scotland. You will be responsible for leading the Medical Affairs department (8 line reports) for all activities within the UK & Ireland including the launch of a novel product later this year. The role includes leading key medical activities relating to a marketed and pre-launch product portfolio along with overall leadership of medical and scientific input in to the companies commercial strategy.
Regulatory Affairs Director - New York City
New York
Feb 14
Regulatory Affairs Director Excellent senior opportunity within a clinical stage biotech based in New York City. Role/Responsibilities The Regulatory Affairs Director will be responsible for...
Senior / Executive Medical Director, Pharmacovigilance
King Of Prussia
Feb 14
Senior / Executive Medical Director, Pharmacovigilance (MD required) Senior / Executive Medical Director, Pharmacovigilance$240,000 - $270,000 + EXCELLENT BONUS + BENEFITS!A growing and international pharmaceutical company is looking...
Senior Specialist Programmer
South East
Feb 14
Stephanie Maccioni is currently recruiting for a Senior Specialist Programmer to join a global Pharmaceutical company for a 12 month contract. The position offers remote...
New Clinical Development opportunity
England
Feb 14
Exclusive Neuroscience opportunity.
Clinical Project Manager - Freelance - Small CRO - Munich (m/w)
München
Feb 14
Clinical Project Manager - Freelance - Small CRO - Munich (m/w) I am currently recruiting for an experienced Clinical Project Manager to join one of my clients, a small clinical research organisation, at their subsidiary in Munich. Due to extensive work load they are looking for someone to support their clinical research team for the initial period of 6 months with a possibility of extension by another 6-12 months. ...
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Senior Study Specialist – Dutch/Belgian border – 12 Mths +
Netherlands
Feb 14
Senior Study Specialist – Dutch/Belgian border – 12 Mths + CRA, Research, Study, Cardiovascular, Pumps, Cylinders, Drug delivery, Clinical Studies, Research, Trials, Project Manager, Project Leader, Continuous Improvement, Service Orientated, Stakeholder Management, Senior, Dutch, English, Biotech, Pharmaceuticals, CRO, Post market, Registration, Monitoring, FDA Audits, FDA, Monitor, Protocols, Site Selection, Initiation. ...
CTA - Global brand (NL)
Netherlands
Feb 14
Clinical Study Specialist/Junior CRA - Global Brand - NL Our busy, international Pharmaceutical client is in need of a Junior CRA/Monitor Support Specialist to join one of their Clinical study teams urgently in a varied and challenging role. This role offers the chance to work from home 1, possibly 2 days per week. My client is looking to bring someone on for around 6-12 months and be involved in a variety of interesting/varied projects.
Senior CMC Regulatory Affairs Manager – Pharmaceutical consulting company - Munich – up to 140,000 €
Germany
Feb 13
We are looking for an experienced CMC Regulatory Affairs Manager, who wants to use his knowledge in an well established consulting company with a broad varieties of projects in US and Europe. You can expect an open environment, exciting projects and superb benefits inclusive an opportunity of flexible home-based working.
Executive Director of Regulatory Affairs.
England
Feb 13
The consultant running this executive search is Sam Murphy. For more information or to apply to the position please contact Sam via email – sam.murphy@tecgroup.net
Senior Vice President of Global Regulatory Affairs
England
Feb 13
This position is retained by Sam Murphy of TEC Group. For more information on this position or any other global regulatory position please speak to Sam Murphy our Senior Consultant for Global Regulatory Affairs. 0044 (0) 208 544 34 23 / sam.murphy@tecgroup.net
Regional Medical Affairs Director Cardiovascular
Germany
Feb 13
RBW Consulting are working in partnership with a Large Global Pharmaceutical Company to recruit a Cardiovascular Medical Affairs specialist for a permanent position to be based in Germany.
Director Regulatory Affairs, Development
Bridgewater, NJ
Feb 13
For more information on the above role, please do not hesitate to get in touch today with RBW Consulting today. You can find us directly on +1 (646) 586 9087, or contact the consultant directly on ross.apted@rbwconsulting.com for a confidential chat.
Medical Information Operations Manager - Weybridge
Surrey
Feb 13
Mary Bolt is recruiting for an Operations Manager, Medical Information to join a World leading pharmaceutical industry on a contract basis. The role will have...
Chief Medical Officer – Vaccines and Neurology - Austria
austria
Feb 11
We have a fantastic opportunity available as the Senior Director at an incredibly promising startup biopharmaceutical company. This is the perfect opportunity for an experienced medical specialist within the field of Vaccines and Infectious diseases to enter into a senior position within an organization which are set for big things in the future.
Director, Global Medical Affairs Lead Dermatology – Home - based or office based
uk,france, germany, switzerland, usa, Ntherlands
Feb 11
The Director Global Medical Affairs leader will be responsible for providing scientific direction, execution and support to the VP, GML for life cycle management of new indications in Dermatology.
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Medical Monitor
San Francisco
Feb 10
Medical Monitor Needed for Expanding Pharma Firm  Medical Monitoring | OncologyGreater Newark, CA Area$265,000 - $365,000 + bonus +complete benefits packageAn expanding pharma company is...
Head of Medical Affairs
UK
Feb 10
Excellent opportunity for a Head of Medical Affairs
Veterinary Clinical Pathologist
Harrogate
Feb 10
Due to our continuous growth, we are looking for an experienced Veterinary Clinical Pathologist to be based at our Harrogate site in United Kingdon.
Head of Drug Product Manufacturing Science and Technology
Lausanne
Feb 9
Head of Drug Product Manufacturing Science and Technology (Biologics) Switzerland (French Speaking Area) Job Summary: Hydrogen Group has been asked to assist in the hire of a Head of Drug Product Manufacturing Science and Technology (Biologics) to join a global biopharmaceutical company with state of the art facilities across the globe. This is a management post based in the French speaking part of Switzerland. ...
Medical Director – Medical Affairs
London
Feb 8
Are you a dynamic medical affairs physician who is looking for a move within Pharma industry and have a broad skill base within Medical Affairs, PVG, Safety and Regs?
Clinical Project Director (Line Manager CPMs)
Basel
Feb 8
We are looking for an experienced Clinical Project Director/Clinical Research Manager with a pharmaceutical background with extensive experience line managing CPM's and/or Study Managers
Project Statistician
West London
Feb 7
One of my top 10 pharma clients have chosen Aerotek to recruit for them to add to their industry leading stats team. This position will sit in the oncology team, this area is rated in the top 10 in the world and continues to climb up the rankings and boasts one of the best oncology pipelines in the industry.
Principal Contract Statistical Programmer - Home-based
Cambridge
Feb 7
My client, one of the biggest pharmas around have chosen Aerotek to recruit on behalf of them for multiple contract principal programing positions. The positions are all 100% home-based and are spread across a range of therpeutic areas, with oncology being the most prominant. For this position you will be required to lead, not only a team but a project as well, alongside managing vendors. ...
Principal Statistician - Uxbridge
Uxbridge
Feb 7
Stephanie Maccioni is currently recruiting for a Principal Statistician to join a world leading global Pharmaceutical company for a 6 month contract. The role will...
Quality Assurance Manager, Pharmacovigilance
Slough
Feb 6
Quality Assurance Manager, Pharmacovigilance GPvP / Quality Assurance Quality Systems / Pharmacovigilance / GPvP / Health Authorities / Health Inspection Audits / Quality Management System / System Design / Content / Regulatory / GPvP / Global Patient Safety / GPS / GRDQ / EasyDoc / CAPA / SME / Safety / Pharmaceutical / Development / My client are a leading global pharmaceutical company with revenue exceeding one and a half billion Euros.
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New Inflammation Opportunity
England
Feb 6
New Clinical Development opportunity
New Inflammation Opportunity
England
Feb 6
New Clinical Development opportunity
New Inflammation Opportunity
England
Feb 6
New Clinical Development opportunity
New Clinical Development opportunity
England
Feb 6
New Inflammation opportunity
New Clinical Development opportunity
England
Feb 6
New Inflammation opportunity
Director Dermatology (psoriasis) Global €200,000 plus Package Car, Bonus, Pension
uk,france, germany, switzerland, usa, Ntherlands
Feb 3
Top 10 pharma company with an excellent pipeline in Dermatology (psoriasis). This role will lead the pre-launch and launch activities for these developments across Europe including some emerging markets
HEOR MSL Needed for Expanding Pharma
New Jersey
Feb 3
HEOR Medical Science Liaison Needed for Expanding Pharma CompanyInfectious Disease | Rare Diseases | HEOR Greater New York Area$165,000 - $200,000 + bonus +complete benefits packageAn...
Active Quality Auditor
Frankfurt am Main
Feb 3
Active Quality Auditor  – DACH Region (Home Office) The client is looking for a Quality Auditor based in the DACH region. Being one of the...
Experienced Market Access Consultant/Project Manager
London
Feb 2
rbatchelor@barringtonjames.com +44 (0) 1293 776644
Senior Programmers required to support an Oncology Project
England
Feb 2
I'm currently engaged with a very reputable pharmaceutical organisation in the UK who are actively looking to hire a senior sas programmer for a unique position.Large Pharmaceutical12 MonthsUp to £65 / hourHome working can be offered for the right candidateOncology experience is required
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SAD/ Assoc. Director - Behavioural Change - London
South West London
Feb 1
An innovative, independant healthcare communications agency with a holistic approach based in Central London is seeking an experienced Senior Account Director/ Associate Director to join...
European Market-Access Director / 6 Month Contract.
Germany
Jan 31
This position is a great career opportunity for the right candidate to work within a well-established, growing team, and work with innovative, ground breaking technologies to add to your portfolio.
R E G U L A T O R Y CMC Large Molecule Lausanne Vevey area RA CMC Bio strategy for a P2B to P3 molecule Senior RA CMC Manager
Southern Switzerland
Jan 30
This role is on exclusive assignment to Advanced Search & Selection. Please contact Theo Moore or Matt Greig initially on +44 20 7801 3380 or +44 7918 679 405 (until 9.00 pm CET and Saturday mornings) or send a full CV and contact information to theo@advregulatory.com or matt.greig@advregulatory.com who will support your assessment and on boarding process.
Regulatory Director Oncology Work on a major P3 programme for a NME (ADCs and mAbs) Northern Europe Great salary and relocation package
Northern Europe
Jan 30
This role is a project level role with a great team around you, and is the designated EU RL with long term opportunities to step in to a GRL role if you prove well. The position is within a company spending in excess 1.3 USD billion on R and D every year in Oncology and this company has 4 NMEs at EOP2 ... [please read]
OPTION BELGIQUE Regulatory Team Director Manage a team for a mAb for new indications and market expansion Successful team Direct reports
France
Jan 30
I am seeking an individual who has both a great deal of empathy and vision to manage a successful team based in mainland Europe, and the UK, for the Member state and extended European region. The role is first and foremost about managing people ... (please read)
Associate Principal Consultant of Market Access for a Leading Consultancy
London
Jan 28
Send your CV over to Reece Batchelor at rbatchelor@barringtonjames.com or give Reece Batchelor a call on +44 (0)1293 776644 for more information. Perhaps you know of someone else who may be interested? Barrington James pays a £500/€500 reward per successfully placed candidate that we aren’t aware of and is referred by you! So it’s worth getting in touch.
Medical Director Dermatology
Belgium
Jan 25
A top global pharmaceutical organisation is looking to bring on board an experienced professional within Medical Affairs to join their teams as a Medical Director...
Medical Director – Pneumology / Pulmonology / Respiratory
field based in Germany
Jan 20
As the Medical Director you will act as the conduit for accurate, unbiased and updated clinical, scientific and medical information between the external scientific community in Germany and the company.
Senior CMC Specialist
Switzerland
Jan 20
Senior CMC Specialist. Are you an experienced CMC expert with a solid Scientific background looking for your next opportunity in Basel? Would you be interested in working with some of the biggest names in our industry and getting involved in ground breaking products?
Head of Medical Affairs - Rare Disease
Hertfordshire
Jan 18
An exciting biopharmaceutical company who are setting up their operations across Europe are seeking a Head of Medical Affairs, UK and ROI. As a specialist...
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