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The latest Executive Pharmaceutical Jobs jobs - BETA

Jobs: (Executive Pharmaceutical Jobs)

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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...
Senior QA Specialist (contract)
Utrecht
Feb 20
Senior Quality Assurance Specialist - Netherlands - €80-90/hrOptimus 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 related to management of Good Manufacturing Practice (GMP) and Quality Assurance activities.You will receive the opportunity to lead the QA team, consisting of 5 other officers. ...
Consultant Senior Statistical Programmer - Switzerland
Switzerland
Feb 20
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.
Head of Quality - Qualified Person
Switzerland
Feb 20
Head of Quality Assurance – Switzerland – up to CHF150,000 p/aOptimus Life Sciences is working with a bio-pharmaceutical start-up client to find a Head of Quality Assurance to join the senior management team, providing oversight of the QA team across a highly regulated GMP manufacturing facility. Tasks and Responsibilities: * Manage the strategic and operational performance of the Quality Assurance department. ...
Senior SAS Programmer - 12 month contract, Switzerland
Basel
Feb 20
An excellent opportunity has arisen for a Senior SAS Programmer to join an experienced team based within a leading Pharmaceutical company based in Switzerland. This will be on a 12 month contract basis and is paying an excellent daily rate of up to 1,100CHF.
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. ...
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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.
Clinical Project Manager - 12 month Contract
Cambridge
Feb 20
Urgent opportunity for a Clinical Project Manager to join a pharmaceutical company based in Cambridge for an initial 12 month contract. The Clinical Project Manager will be responsible for the management of phase I-IV clinical trials across various therapeutic areas ensuring that are meeting ICH/ GCP guidelines.This role is a field based opportunity and requires travelling, therefore the right candidate must have a driving licence.
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...
Swiss Commercial Manager-Hospital focus-Swiss
Geneva
Feb 17
Swiss Commercial Manager-Hospital focus-SwissNonStop`s client is a Internationally renewed company in the area of Infectious diseases. They take pride in the quality of their products which they bring to the market from their own research and development. They have manufacturing sites in the US and Switzerland and are looking forward to developing the markets for their pipeline products.
QA Auditor (contract)
London
Feb 17
QA Auditor (12-months contract) – London – £70/hr Optimus Life Sciences have partnered with a pharmaceutical CMO company in the UK to find an Interim Quality Assurance Auditor. Reporting to the Head of Quality, you will primarily focus on the inspecting the manufacturing site and our CMO partners. Tasks: * Evaluate existing Quality Management System (QMS) and update to improve medicinal quality. ...
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.
Associate Director Regulatory Affairs for Pediatric Development – global pharma company – Frankfurt – up to 130,000 € - some home flex available
Germany
Feb 17
Do you want to be in the front line with us against cancer on children? Then get in touch - we are looking for an experienced Regulatory Affairs Manager, who wants to use his knowledge about paediatric development in one of the biggest pharmaceutical organizations worldwide. You can expect an open environment, life-changing projects and excellent benefits.
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. ...
Regional Head of compliance and ethic
Paris
Feb 16
A leading Pharmaceutical company has a requirement for;Regional Head of compliance and ethic - France + BeneluxPermanent position, Full timeOffice based in ParisLine management: yesSalary: 160000 - 180000 Euros + bonusStart Date: Flexible for the right candidateIf you want to discuss about this job you can contact me at juliette.wagner@secpharma.com with your contact number and best availability for a confidential phone conversation.
Clinical Operations Director - Zurich area - 12 months + (m/w)
Switzerland
Feb 16
Clinical Operations Director - Zurich area - 12 months+ (m/w)Amoria Bond is recruiting a skilled Clinical Operations Director for a pharmaceutical company in Switzerland. Purpose of this role is to provide research expertise to all essential aspects of the clinical trial, as well as assisting with setting up the Project and Trial frameworks. ...
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...
Contract Qualified Person
London
Feb 15
Qualified Person QP – London – up to £900 per day Optimus Life Sciences is working with a multinational bio-pharmaceutical client to find a Qualified Person to join their manufacturing site. Reporting directly to the Head of Quality, you will primarily focus on the batch-release of sterile vaccines (approx. 30 per month). Quality Assurance management experience is a bonus. Tasks: * Provide QP batch-release of product(s) to market. ...
Contract Qualified Person
Yorkshire and the Humber
Feb 15
Qualified Person (QP) – Yorkshire – up to £750 per day Optimus Life Sciences is working with pharmaceutical company to find a Qualified Person to join their manufacturing site full-time. Reporting directly to the Head of Quality, you will focus on the batch-release of solid-dose products and ensure GDP compliance at the site. You will work alongside one other Qualified Person, and receive support from 3 QA Officers in a fast-paced working environment. ...
Contract Qualified Person
Breda
Feb 15
Qualified Person QP – Breda (Netherlands) 12-month contract: €1,000 per day Optimus Life Sciences is working with a multinational CMO to find a Qualified Person on a 12-month contract.You will be required on-site for a minimum of 2 days/week to provide QP support to the QA department. . Tasks: * To implement QP batch-release of product(s) to market as required. ...
Medical Sciences Liaison - Switzerland - 9 months (m/w)
Switzerland
Feb 15
(Interim) Medical Sciences Liaison - Switzerland - 9 months (m/w)One of our international clients is looking for a Medical Scientific Liaison to support their team at their subsidiary in Switzerland. The purpose of this role is to provide strategies and plans with regards to budget control and scientific projects within our clients oncology department. ...
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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.
Principal SAS Programmer Consultant - Remote Worker from the UK
England
Feb 15
I'm currently engaged with a very reputable pharmaceutical organisation in the UK who are actively looking to hire a Principal SAS programmer to support a number of key Oncology studies.Large Pharmaceutical 12 Months Up to £60 / hourHome working is permitted from the UKOncology experience is required
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...
Associate Director - International Regulatory Strategy Lead
Switzerland
Feb 14
A global, highly specialised Biopharmaceutical company based in Switzerland are growing in size. They have reorganised their Regulatory Affairs division to accommodate a growth in business and product portfolio. New positions have been created in two therapy areas - Neuroscience and Genetic Disease. Your job title in this position will be Associate Director - International Regulatory Strategy Lead and you will report into the Head of the group directly.
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. ...
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.
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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...
Global Consumer Insights Manager-Swiss
Switzerland
Feb 12
Global Consumer Insights Manager -Direct to Consumer-SwissDo you have passion about working in Consumer Insights/ B2B and B2C environment? For those specialists with background and experience in Consumer insights and B2B and B2C Marketing we are happy to offer an exciting opportunity to join a Multinational company with Global Operations where you can have your saying.
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.
Medical Monitor
San Francisco
Feb 10
Medical Monitor Needed for Expanding Pharma FirmMedical Monitoring | OncologyGreater Newark, CA Area$265,000 - $365,000 + bonus +complete benefits packageAn expanding pharma company is...
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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.
Active Quality Auditor and Functional Safety
Munich
Feb 9
Quality Auditor/Functional Safety (Active Medical Devices)  – Munich The client is looking for a Quality Auditor with specialist knowledge of Active  Devices and/or Functional Safety...
Senior Medical Director Oncology
France
Feb 9
This Senior Medical Director will be responsible for the development, and execution of country medical strategies for a Global Pharmaceutical Organisation with a strong pipeline...
Medical Director - Oncology
Austria
Feb 9
The Medical Director is looked to as a leading figure within our organisation and will be expected to manage a small team within Medical Affairs...
Senior Medical Affairs Director - EMEA
London
Feb 9
An entrepreneurial, mid-sized Biopharmaceutical company is seeking to hire a Senior Medical Affairs Director to develop and execute high quality Regional Medical strategies and operational...
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. ...
Clinical Project Manager
United States
Feb 8
Clinical Project Manager – Mid-sized, global CRO with the chance to make a greater impact on the community – Greater Boston Area Job Description Clinical...
Contract Qualified Person
Republic of Ireland
Feb 8
Qualified Person – Republic of Ireland – up to €1,000 per day Optimus Life Sciences have partnered with a bio-pharmaceutical CDMO to find a Qualified Person.Reporting directly to the Head of Quality, you will primarily focus on the safe administration of Investigational Medicinal Products (IMPs) on a weekly basis (sterile and non-sterile), and provide supervision to 10 Quality Assurance Officers. ...
Validation Engineer
Basel
Feb 8
Urgent 9 Month Contract for worldwide leading Pharma Company. The Role will include:Managing Complexity/Technical AccountabilityServes as technical expert for the Validation process and...
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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
Global HEOR Director
High Wycombe
Feb 8
My client is a fast-growing global mid-sized Biopharma company with products across numerous therapy areas. They have grown rapidly over the last few years, a...
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. ...
Oncology Medical Advisor
Switzerland
Feb 7
We are currently representing one of the largest global pharmaceutical organisations in the world who are looking to expand their Medical Affairs teams in the...
Medical Advisor - Immuno-Oncology
Switzerland
Feb 7
We are currently representing one of the largest global pharmaceutical organisations in the world who are looking to expand their Medical Affairs teams in the...
Pharmaceutical Senior Product Manager
Alameda
Feb 7
Our client, specialty pharmaceutical company which mainly markets products for treatment in neurology, pain and diseases of the central nervous system, is currently looking to...
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...
Clinical Data Manager - Duesseldorf- SAS/CDISC (m/w)
Düsseldorf
Feb 7
Clinical Data Manager - Dusseldorf - 9 months - SAS/CDISC (m/w)For one of our clients I am currently looking for a skilled Pharmaceutical Data Manager with a background in the pharmaceutical or Life Science sector. Our client is a medium sized CRO based in the Dusseldorf area in Germany, that focuses on biostatistics and clinical data analysis. They are currently looking for a Data Manager to support their research team by setting up relevant databases and by conducting data analysis. ...
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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.
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 | HEORGreater New York Area$165,000 - $185,000 + bonus +complete benefits packageAn...
Experienced Market Access Consultant/Project Manager
London
Feb 2
rbatchelor@barringtonjames.com +44 (0) 1293 776644
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.
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Senior SAS Programmer - Beerse
Beerse
Jan 31
Anetta Kotynska is currently recruiting for a Senior SAS Programmer to join a Blue-chip pharmaceutical company on a 6 month contract basis. The role is...
Global IT Director–Automation Company –Lucerne/Zug
Zug
Jan 31
Global IT Director – International Automation Company – Lucerne/Zug Keywords: IT, Director, Head, Global, Industry 4.0, Internet of Things, Digitalisation As the Global IT Director, you possess the following qualifications: * Higher studies in Computer Science or a related topic; * Experience implementing global applications * Experience managing local/international IT teams; * You are capable of implementing digital transformation: Industry 4. ...
European Market Access Associate Director
Basel
Jan 30
As an Associate Director you will be a key team member in the European market access function responsible for determining and setting the European market access strategy. In addition to setting the European market access strategy you will also help to create European level market access resources such as value dossiers. You will then work with the affiliates on implementing the market access strategy to maximise reimbursement.
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.
Associate Principal Consultant of Market Access
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.
NEW Global Regulatory CMC Director role with Team Leading – Full project lifecycle (P2a to MAA and L/cycle)
Brussels
Jan 27
Reporting into the Global Head of CMC, and operating on the Global CMC leadership team you will also manage a team of six regulatory professionals at RA Manager, Snr Manager and Associate Director level around global development strategies, MAA activities and new indications/lifecycle initiatives. Please contact theo Moore or Matt Greig on +44 207 801 3384
Interim HEOR Consultant - 4-6 Month Project - Big Pharma
Greater London
Jan 27
Interim – Health Economics / HEOR  Consultant – 4-6 months (dependent on project length)My client, an international pharmaceutical company based in West London/Middlesex are looking for an interim HEOR manager to join their team.This is a fantastic opportunity as the client are looking for a consultant they have not worked with before to create a strong relationship for the future. The role is particularly varied and could cover a wide variety of strategic inputs and responsibilities. ...
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Senior Clinical Study Manager - Belgium
Belgium
Jan 25
I am currently partnered with a small yet well-established and heavily financed Belgian Biotech that are looking for a strong Senior Clinical Manager to come and take control of their Rare Disease portfolio. The person needs to be entrepreneurial, confident and influential over the internal team and external vendors. 2 of the studies within the portfolio have just crossed in to PhII (1 in December and 1 due Q1 this year) with the other following closely behind.
Regulatory Affairs Manager - Marlow
Marlow
Jan 25
Oliver Care is recruiting for a Regulatory Affairs Manager to join a company in the Pharmaceutical industry at their site based in Buckinghamshire on a...
Clinical Study Manager -work from home (12 mths)
Limburg
Jan 25
Clinical Study Manager/Senior Clinical Project manager - (Work from home/Limburg)Study Manager, Trial manager, Project manager, CRA, Research, Study documentation, Study, Cardiovascular, Valves, Medical Devices, Pumps, Cylinders, Clinical Studies, Drug delivery, Therapeutics, Disease, Research, Trials, Project Manager, Project Leader, Continuous Improvement, Service Orientated, Stakeholder Management, Senior, Dutch, English, Biotech, Pharmaceuticals, CRO, Post market, Registration, Monitorin ...
Senior Director, Clinical Regulatory Consulting - Europe
England
Jan 24
A leading consultancy is searching for a European regulatory strategic lead to join their team.
Senior Medical Director, CNS
Dusseldorf, Germany
Jan 24
As a $1.4 Billion revenue, 4000 + employee, family run business this company is genuinely one of the true success stories to come out of the German Biopharmaceutical market. This company have built a hugely successful business that has grown consistently for more than 60 years. Still owned by the original family, this company enjoy employing one of the most impressive leadership teams seen in any mid-large biopharma company.
Clinical Trial Manager / Senior - Small Exciting Biotech, Oncology I/IIa - Central New Jersey
Central New Jersey / 1-2 days home flex
Jan 21
Clinical study manager, CTM – Exclusive new Clinical Trial Manager position is available within a dynamic, exciting small Biotech organization specializing in the Oncology space. Working from their Central New Jersey HQ, joining this company of 15, you will work across the full lifecycle in Phase I/IIa studies – design, protocol, vendor selection and management and budget involvement. Happy to consider Senior CTMs as well – suited to those who want a growing, engaging and exciting CTM role.
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?
Global Medical Affairs Director Cardiology, Neurology and Respiratory – London, Surrey £120,000 basic
uk,france, germany, switzerland, usa, Ntherlands
Jan 11
My client are offering experienced candidates who have a great background in Cardiology, Neurology and Respiratory a fantastic opportunity to have a strategic influence into the growth of their company.
Global Head - Biomarker Group Leader – Taking a Biotech from preclinical to clinical stage – Immunology
Belgium, Nerherlands
Jan 11
We have an exciting opportunity available as a Group Leader of Biomarker and Translational Medicine at an exciting biotech based in Belgium. This is a fantastic opportunity for an experienced scientific professional to enter into a strategic senior position with project design and implementation responsibility.
jobs : 100 +
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