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The latest Executive Pharmaceutical Jobs jobs - BETA

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Associate Director, Global Regulatory Affairs; Immuno-Oncology
USA
Apr 27
For more info please call Sam Murphy on 0044 208 544 3423 / sam.murphy@tecgroup.net
Director, Global Regulatory Affairs; Immuno-Oncology
Boston MA
Apr 27
Tec Group international has partnered with a global Pharmaceutical company to find a regulatory profile to help lead the business and Regulatory departments. This position offers a creative platform for the chosen candidate to work on projects and areas they excel in. This position is based in Boston and offer a competitive salary and package. For more info please contact Sam Murphy at TEC Group sam.murphy@tecgroup.net
Statistician / Senior Statistician (Contract or Permanent)
San Diego
Apr 27
For more information on this position please contact Sam Murphy via sam.murphy@tecgroup.net / 0044 (0) 208 544 3423
Senior Medical Director - Medical Communications
San Francisco
Apr 27
Agency dedicated to medical content development for promotional educational programs is seeking a Senior Scientific Director with experience in using strategic initiatives to develop and...
Senior Medical Director
New York
Apr 26
Job Summary:  High Growth Medical Communication agency looking for Senior Medical Director (Full Time) to produce leading scientific content in a variety of therapeutic...
Medical Director
Chicago
Apr 26
Job descriptionHigh growth Medical Communications agency in Chicago looking for a Medical Director (full time). As Medical Director, you will be leading content creation...
Medical Manager - Immunology
United Kingdom
Apr 26
We are working with a global pharmaceutical organisation that has one of the strongest reputations within the UK and are currently looking to expand their...
Clinical Research Manager - Phase II+III - Frankfurt (m/w)
Frankfurt am Main
Apr 26
Clinical Research Manager - Biotech Trials Phase II+III - Frankfurt (m/w)Amoria Bond is looking for a Clinical Project Manager to join one of our international clients at their subsidiary based in Germany. Purpose of this role is to set up and manage a Phase II and III clinical trial for the whole duration. ...
Senior Quality Manager
Berlin
Apr 26
 I am currently working on a Senior Quality Manager Rolle based in Germany: Berlin The Company·         Global leading provider of innovative solutions·         Building...
Global Medical Affairs Lead – New Product Launch Neuroscience – CNS
Europe
Apr 26
This rapidly expanding Pharma is seeking a medic to guide the launch of a new CNS product and manage the coordination and development of the Global Medical Plan in conjunction with the marketing team. Work in an environment where the employees are passionate about their contribution to the Neuroscience patient community.
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Executive Lead – API Sourcing
Europe
Apr 26
This rapidly expanding Pharma is looking for an experienced Pharma Sourcing and procurement expert who has API experience. This role would involve identifying short and long term sourcing opportunities, developing cost reduction strategies, leading supplier evaluations and contract negotiations, leveraging market intelligence and engaging with internal and external business partners.
Teamlead Regulatory Affairs Medical Devices - Flache Hierarchien
Frankfurt am Main
Apr 25
Eine einmalige Gelegenheit Ihre Kompetenzen aus Regulatory Affairs und Qualitaetsmanagement in einem innovativen Unternehmen einzubringen und das Wachstum weiter auszubauen. Arbeiten bei einem dynamischen und...
Senior Director position for Medical Doctor, Board Certified Neurologist
Germany
Apr 25
We are currently representing a top 3 Global Pharmaceutical organisation as they seek to bring on board an experienced Medical Affairs professional in the field...
Director Payer Insights and Access - Tadworth
Tadworth
Apr 25
Hendre Moolman is recruiting for a Payer Insights & Market Access contractor to join a research based pharmaceutical company at their site based in Tadworth,...
Drug Safety and MI Manager - Hemel Hempstead
Hemel Hempstead
Apr 25
Hendre Moolman is recruiting for a Pharmacovigilance and Medical Information Manager to join a speciality pharmaceutical company at their site based in Hemel Hempstead on...
International Senior Medical Director, Emerging Markets
London
Apr 25
An exciting opportunity for a Senior Medical Director has arisen at an above country level within a global Biopharmaceutical company based in the UK.Aligned /...
CEEMEA Commercial Franchise Head (CNS and Pain)
Germany
Apr 25
OverviewWe are currently looking for a highly commercially minded individual take full P&L accountability for our client’s CNS and Pain portfolio within the CEEMEA region and to drive optimal ‘go to market strategies’ and profitable growth within this area. This is an excellent opportunity be fully accountable for a portfolio worth $hundreds million with the opportunity to rapidly progress in your career; such as into a Global, General Manager or a Country Head role. ...
CEEMEA Franchise Head - CNS / Pain therapeutic area
Germany
Apr 24
Reporting to the CEEMEA Head of Marketing, you will have P&L responsibility for your region within the CNS/Pain therapy area portfolio under your remit.With no direct line management in this role, you will use your experience of influencing across a complex matrix organisation, supporting the needs of the countries while successfully driving market share growth across the diverse portfolio. ...
Global Regulatory CMC Expert - Biologics
Geneva
Apr 24
A renowned and world leading Pharma company with global reach are searching for a CMC expert. The CMC expert is in largely an operational role. This is a great opportunity for someone taking their first steps into Switzerland and would benefit a professional looking to make some positive changes to gain international experience working with one of the leading companies in the life science industry.
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Head of Project Management - Rapidly Expanding CMO - Cell Therapy - Netherlands - EXCLUSIVE
Netherlands
Apr 24
Are you looking for the opportunity to join a rapidly expanding CMO with a drive for cell therapy and regenerative medicine? Want to manage and grow a passionate project management team? have the desire to influence to direction of an up and coming company? Then apply today.
Senior Programmer - Uxbridge
Uxbridge
Apr 24
Stephanie Maccioni is looking for a Senior Programmer to join a Global Biotech company on a 12 month contract to be based on site in...
Indikationsuebergreifende/r medizinsiche/r Direktor/in - Rheumatologie and Dermatologie
Germany
Apr 24
Nutzen Sie diese Gelegenheit als Einstieg in die Industrie und bereichern Sie das medizinisch-wissenschaftliche Team in der bedeutesten Laendergesellschaft des Konzerns als indikationsuebergreifende/r medizinsiche/r Direktor/in in Rheumatologie & Dermatologie. Festanstellung im Rhein-Main-Gebiet.
Global Pricing Senior Manager / Director (based anywhere in Europe)
London
Apr 22
Our client is a market-leading Global Medical Devices & Technology company. With close to 50 years of history in this field they have a wealth...
Senior Medical Director
New Jersey
Apr 21
Job Summary:  High growth Medical Communication agency seeking full-time Senior Medical Director to deliver scientific services and products in a variety of therapeutic categories. ...
Drug Safety Physician (6 Months - UK South East)
London
Apr 21
*****DRUG SAFETY PHYSICIAN (6 MONTH CONTRACT - UK - SOUTH EAST)*****JOB OVERVIEW:- Job Title: Drug Safety Physician (freelance)- Rate: £60 per hour- Company: Pharmaceutical- Office Location: West London, South East- Contract Length: 6 months (possibility of an extension)- Contract Type: Full time, office based (predominantly)- Start Date: 1st May 2017RESPONSIBILITIES:- Medical responsibility for the safety governance, risk management & technical activities- Thorough & professional support fo ...
EU Market Access Director - Innovative Biotechnology
Switzerland
Apr 21
NEW OPPORTUNITY - For a Market Access Leader to join an innovative Biotechnology company
EU Market Access Director - Rare Diseases
Sweden
Apr 21
NEW OPPORTUNITY - For a Market Access Leader to join an innovative Biotechnology company within Rare Diseases
EU Market Access Director
UK
Apr 21
NEW OPPORTUNITY - For a Market Access Leader to join an innovative Biotechnology company
Senior Regulatory Affairs Specialist
Somerset, NJ
Apr 21
I manage a range of other permanent and freelance positions for a broad portfolio of clients, so if the above role isn’t for you but you’d nevertheless like to discuss other opportunities currently available both now and in the near future, we are happy to get in touch at your discretion. Contact Ross Apted at 617 982 1238 today!
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Manager, Regulatory Affairs
Piscataway, New Jersey
Apr 21
I manage a range of other permanent and freelance positions for a broad portfolio of clients, so if the above role isn’t for you but you’d nevertheless like to discuss other opportunities currently available both now and in the near future, we are happy to get in touch at your discretion. Contact Ross Apted at 617 982 1238 today!
Medical Advisor - Rheumatology
South East
Apr 20
Medical Advisor - Rheumatology A Top 10 global pharmaceutical company with a major presence in Europe are looking to appoint a Medical Advisor for the UK medical team, joining with a focus on Rheumatology and being involved in an upcoming product launch
Director RA / QA Medical Devices - dynamisches Familienunternehmen
Stuttgart
Apr 20
Eine einmalige Gelegenheit Ihre Kompetenzen aus Regulatory Affairs und Qualitaetsmanagement in einem innovativen Unternehmen einzubringen und das Wachstum weiter auszubauen. Arbeiten bei einem dynamischen und...
FREELANCE Senior Programmer - Switzerland
Switzerland
Apr 20
A 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.
Manager, Regulatory Affairs Strategy- Oncology
New Jersey
Apr 20
I manage a range of other permanent and freelance positions for a broad portfolio of clients, so if the above role isn’t for you but you’d nevertheless like to discuss other opportunities currently available both now and in the near future, we are happy to get in touch at your discretion. Contact Ross Apted at 617 982 1238 today!
Study Manager - Netherlands
Netherlands
Apr 20
Study Specialist/Senior CRA - Netherlands CRA, Research, Study, Clinical Studies, Research, Trials, Project Manager, Project Leader, Continuous Improvement, Service Orientated, Stakeholder Management, Senior, Dutch, English, Biotech, Pharmaceuticals, CRO, Post market, Registration, Monitoring, pre-market, post-market. An experienced, has some experience in team lead, mentoring and training capacity as a Senior Clinical Project manager/Study Manager. ...
Leitung Medical Affairs Europe
Germany
Apr 19
Nutzen Sie die Gelegenheit in dieser einmaligen, neuen Herausfordeurng und bereichern Sie das Management-Team Deutschland, Österreich und Emerging Europe in der Position als Leitung Medical Affairs Europe in einer Festanstellung im Rhein-Main-Gebiet.
Quality Assurance Junior Manager
Bern
Apr 19
This Quality Assurance Junior Manager job is with one of the most renowned global pharmaceutical, medical device and consumer health organisations located in Bern, Switzerland. The organisation is a top 10 pharma company and employs over 100,000 professionals worldwide.Role Responsibilities: Ensuring that products, materials for production, systems and facilities are in state of sustainable compliance with the requirements of GMP and regulatory authorities. ...
SAS Programmer - Switzerland - 12 Months Contract
Basel
Apr 19
One of our clients, a renowned pharma company, is currently looking for an experienced SAS Programmer to join their dynamic team on-site in Basel, Switzerland.
Manager, Global Labelling
Bridgewater, NJ
Apr 19
I manage a range of other permanent and freelance positions for a broad portfolio of clients, so if the above role isn’t for you but you’d nevertheless like to discuss other opportunities currently available both now and in the near future, we are happy to get in touch at your discretion. Contact Ross Apted at 617 982 1238 today!
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Sr. Specialist, Regulatory Affairs
Bridgewater, NJ
Apr 19
The Regulatory Affairs Senior Specialist executes the pharmaceutical regulatory strategies for assigned products. Supports the Regulatory Affairs Senior Manager with regard to submissions and other product development and support activities.
Senior Vice President Commercial - East Coast
USA
Apr 19
We are looking for a Senior VP commercial (with substantial experience in business development within the CRO industry) to help develop and ensure successful implementation of a business development strategy. This job position is full-time and requires location on the East Coast US.
Business Development Director
North Carolina
Apr 19
Experienced CRO Business Development professional required for North Carolina based position in the USA.
Director of Quality
Cork
Apr 18
Director of QualityThe CompanyMy client is the world leader in delivering therapeutics that provide meaningful advances to patients who live with serious and...
Director, Regulatory Affairs
Bridgewater, NJ
Apr 18
The Regulatory Director coordinates and oversees regulatory development and post-approval regulatory activities for US generic (Gx) products.
Associate Director, Regulatory Affairs-CMC
Bridgewater, NJ
Apr 18
The Regulatory Affairs – CMC Associate Director independently manages all regulatory CMC aspects of company Pharmaceuticals products throughout their lifecycle. This includes Brand, Generics, OTC/Nutritionals, Dietary Supplements and Medical Devices. The Associate Director is responsible for the regulatory CMC strategies of all submissions for products under his/her responsibility as well as managing interactions with regulatory authorities on CMC issues.
Clinical Program Manager
Switzerland
Apr 18
We are currently working with a rapidly developing international Biotech that is trying to redefine the way that Diabetes and Oncology are currently treated.Currently,...
Scientific Marketing Manager | Nutrition
Benicia
Apr 18
Multi-Million Biotechnology & Chemicals CompanyLocation: Benicia, CACompensation: $110k - 120k + Bonus + BenefitsOur client, a multinational million dollar biotechnology and chemicals company, is looking...
Market Access and Pricing Manager – European – Rare Diseases.
Flexible Location
Apr 18
I recruit specifically into Health Economics and Market Access positions throughout Europe, if you would like to speak to me regarding one of my current vacancies, or simply be made aware of opportunities as they arise then please call me today on +44 (0)1293 77 66 44 for a confidential discussion.
Statistician / Senior Statistician (Contract or Permanent)
San Diego
Apr 18
For more information on this position please contact Sam Murphy via sam.murphy@tecgroup.net / 0044 (0) 208 544 3423
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Director, Global Regulatory Affairs; Immuno-Oncology
Boston MA
Apr 18
Tec Group international has partnered with a global Pharmaceutical company to find a regulatory profile to help lead the business and Regulatory departments. This position offers a creative platform for the chosen candidate to work on projects and areas they excel in. This position is based in Boston and offer a competitive salary and package. For more info please contact Sam Murphy at TEC Group sam.murphy@tecgroup.net
Associate Director, Global Regulatory Affairs; Immuno-Oncology
USA
Apr 18
For more info please call Sam Murphy on 0044 208 544 3423 / sam.murphy@tecgroup.net
2 x CandQ Engineers - 12-18 Month Contracts - FRANCE
London
Apr 18
**2 x C&Q Engineers Needed****12 – 18 Month Contracts****FRANCE**I am currently looking for 2 x C&Q Engineers for 12-18 Month Contracts to be based in two different locations in France.You must be fluent in French & English to be considered for these positions.Rate: €450 - €500 per dayLocations:1)      Near Paris (30km south)2)      50km south of Lille in Northern FranceGeneral role:-          Ensuring the integration process Engineering, Commissioning and Qualification. ...
Director Commercial Operations Europe - Oncology
Germany
Apr 18
My client an innovative creator and supply of top end pharmaceutical products are currently searching for a Director Commercial Operations for their new Oncology franchise in Munich, Germany.
European Director Medical Affairs Oncology
Hertfordshire
Apr 18
Skills Alliance are exclusively working with a start-up biotech to assign their first European Director Medical Affairs, Oncology. This is a highly visible role with...
Regulatory Affairs Associate
Mahwah
Apr 18
Looking for Regulatory Affairs individuals who are interested in working with a growing pharmaceutical company. This is a contract to hire opportunity with incredible benefits....
Clinical SAS Programmer (SDTM) 12 months contract Basel Switzerland - Global Pharmaceutical
Switzerland
Apr 17
Clinical SAS Programmer (SDTM) 12 months contract Basel Switzerland - Global Pharmaceutical
Sr. Biostatistician (Remote)
San Francisco
Apr 14
Sr. Biostatistician, Needed for Expanding Biotech Company Biostats | Phase I-IV Clinical TrialsWest Coast, Remote$140,000 - $160,000 +complete benefits packageAn expanding pharmaceutical company is...
Account Director; Parsippany NJ
New York
Apr 14
Account Director As the Account Director, you will manage the day-to-day client interactions and development on assigned account(s) by directly overseeing all ongoing projects, ensuring...
Account Director NY
New York
Apr 14
Account Director As Account Director, you will manage the daily growth and client interactions on your assigned account(s). In addition, you will oversee all project /...
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Account Director
San Francisco
Apr 14
Account Director As Account Director, you will manage the daily growth and client interactions on your assigned account(s). In addition, you will oversee all project /...
Product Manager
Dallas
Apr 13
Multi-Million Dollar Life Science CompanyLocation: Fort Worth, TexasCompensation: $110k – 130k + bonus Our client, a world-renowned life sciences company, is looking for a ...
Key Account Manager
San Diego
Apr 13
Key Account Manager As the Key Account Manager, you will manage the day-to-day client interactions and development on assigned account(s) by directly overseeing all ongoing...
West Coast Sales Engineer
Los Angeles
Apr 13
West Coast Sales Manager (Medical Device company) As the West Coast Sales Manager, you will manage the interactions and development on assigned account(s) by directly...
Director QA and Regulatory Affairs (m/w) Europe
Baden Württemberg
Apr 13
Eine einmalige Chance als Ingenieur und Regulatory Affairs Spezialist im Bereich medizinische Geraete der Klassifizierungen 1 bis 3, Teil eines global operierenden Unternehmen zu werden....
Communications Manager (12 Months - West London)
London
Apr 13
*****COMMUNICATIONS MANAGER (12 MONTHS - WEST LONDON)*****JOB OVERVIEW:- Job Title: Communications Manager (freelance)- Rate: £500 per day (flexible) - Company: Large Pharmaceutical- Office Location: West London, South East- Contract Length: 12 months (likelihood of an extension)- Contract Type: Full time, office basedRESPONSIBILITIES:- Develop & implement an internal employee communications strategy- Strengthen employee engagement & retention across the UK and Europe- Lead the daily workflo ...
Communications Senior Manager (12 Months - West London)
London
Apr 13
*****COMMUNICATIONS SENIOR MANAGER (12 MONTHS - WEST LONDON)*****JOB OVERVIEW:- Job Title: Communications Senior Manager (freelance)- Rate: £500 per day (flexible) - Company: Large Pharmaceutical- Office Location: West London, South East- Contract Length: 12 months (likelihood of an extension)- Contract Type: Full time, office basedRESPONSIBILITIES:- Develop & implement an internal employee communications strategy- Strengthen employee engagement & retention across the UK and Europe- Lead the ...
Medical Director
England
Apr 13
*** My client an expanding pharmaceutical company, are looking for a permanent, Medical Director to join their expanding team ***If you are ready to join a team and hit the ground running and receive full time support from your employer then apply now!
Director, Quality Systems Medical Device
Boston
Apr 13
Director, Quality Systems Medical DeviceQMS | ISO 13485Boston$130,000 - $170,000 + excellent benefitsA rapidly growing Biotech company is seeking a Director, Quality Systems in...
Quality Engineer
Zürich
Apr 13
My client is looking for a Non-Active Devices Engineer based in St Gallen, Switzerland. This is a very exciting opportunity to work with a rapidly...
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Data Standards Project Manager - Belgium
Belgium
Apr 13
Stephanie Maccioni is currently recruiting for a Clinical Data Standards Project Manager to join a leading pharmaceutical company on site in Belgium. This is a...
Biostatistician - Belgium
Belgium
Apr 13
Stephanie Maccioni is currently recruiting for a Biostatistician to join a leading pharmaceutical company on site in Belgium. This is a 6 month contract.Main...
Head of Medical Affairs/Medical Affairs Director - Europe - Global Pharma - Central London - 110k+ - Orphan/Generics
Central London
Apr 13
Great opportunity for a GMC registered physician, with extensive medical affairs experience, to join a global pharmaceutical organization based in Central London. This role is mostly strategic, working as part of a global medical team to drive business needs. You will be responsible for oversight of 2 individuals, and a European medical team, and be pivotal in the growth of the medical business, and support of promotional activities.
Business Development Director - Patient Recruitment
USA
Apr 13
My client an International Patient Recruitment provider for clinical trails are expanding and searching for a Business Development Director in North America.
Scientific Director
Parsippany
Apr 13
Leading Medical Communications agency is seeking a Scientific Director with experience in utilizing strategy to develop and implement medical content. As the Scientific Director you...
Regulatory Affairs Manager
Basel
Apr 11
I have a client in BASEL who is looking for a REGULATORY AFFAIRS MANAGER!The company:-          Dental implantable devices -          Looking for someone to...
Quality Control Head
Basel
Apr 11
innovative site has been branded the “new generation” of drug development, computer science and systems. Over the next few years they are looking to add  ...
Associate Director, Labelling
Brookhaven, NJ
Apr 11
I manage a range of other permanent and freelance positions for a broad portfolio of clients, so if the above role isn’t for you but you’d nevertheless like to discuss other opportunities currently available both now and in the near future, we are happy to get in touch at your discretion. Contact Ross Apted at (646) 586 9087 today!
Director of Business Development – USA
USA
Apr 11
Experienced CRO Business Development professional required for home based position in the USA.
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Senior Manager Advertising and Promotional Compliance Regulatory Affairs
Princeton, NJ
Apr 10
I manage a range of other permanent and freelance positions for a broad portfolio of clients, so if the above role isn’t for you but you’d nevertheless like to discuss other opportunities currently available both now and in the near future, we are happy to get in touch at your discretion. Contact Ross Apted at (646) 586 9087 today!
Regulatory CMC Expert - Biologics
Geneva
Apr 10
A renowned and world leading Pharma company with global reach are searching for a CMC expert. The CMC expert in largely an operational role. This is a great opportunity for someone taking their first steps into Switzerland and would benefit a professional looking to make some positive changes to gain international experience working with one of the leading companies in the life science industry.
Pharma QA Specialist – 6 month contract - Switzerland
Switzerland
Apr 10
Our client, a global leader in Vaccine development are looking to hire a QA specialist for their Manufacturing quality team for an initial 6 month contract. We are looking for a German speaking QA specialist with at least 3 years in a Pharma Manufacturing environment who can start in the next 4- 6 weeks.
REGULATORY in ATLANTA, GA Sr Regulatory Manager(s) and Associate Director(s) NEW Opportunities Growing bio-/pharma Relocation Offered
ATL, Georgia
Apr 9
You want to work in a location where there is high nett to cost of living ratio (more disposable income once the bills are paid), a warmer climate, and where housing stock is much more affordable, and spacey!
REGULATORY in RTP, NC Sr Regulatory Manager and Associate Director NEW Opportunities Growing bio-/pharma Relo offered
RTP, NC, Research Triangle Park
Apr 9
This is a stable but growing company, with successive sales QTR on QTR of around 20%, an R&D spend of around approx. 23% and a busy filing plan across all their therapy areas, so this is a good time to join. Please read and respond! Have a great day!
Lab Equipment Validation Specialist - Stevenage
Stevenage
Apr 7
Natasha Young is recruiting for a Lab Equipment Validation Specialist to work with a globally known pharmaceutical company in Stevenage. The Lab Equipment Validation Specialist...
CHINA EX PAT REGULATORY role Asia Pac Reg Lead (Associate Director) and Sr Mngr ALSO Beijing or Shanghai Great team, Ph1-3, MAAs and L/Cycle
China
Apr 7
This is a >> ‘Once In A Lifetime Opportunity’ << to work on an Ex Pat basis in China, in a role that includes leading the strategy and execution of regulatory plans for Asia Pac, with a GREAT SUPPORTIVE PACKAGE AND brilliant local and global leadership teams. This role is OPEN to individuals with existing Regulatory expertise, please read …
Medical Final Signatory - ABPI - Middlesex - Haematology/Oncology - ZINC
Stockley Park
Apr 6
Planet Pharma is a dynamic global solutions provider for the Pharmaceutical industry. Our management team is built around industry experts with over 100 collective years of Clinical Resourcing /recruitment and functional solutions experience.
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Director, Global Regulatory Affairs; Immuno-Oncology
Boston MA
Apr 5
Tec Group international has partnered with a global Pharmaceutical company to find a regulatory profile to help lead the business and Regulatory departments. This position offers a creative platform for the chosen candidate to work on projects and areas they excel in. This position is based in Boston and offer a competitive salary and package. For more info please contact Sam Murphy at TEC Group sam.murphy@tecgroup.net
Associate Director, Global Regulatory Affairs; Immuno-Oncology
USA
Apr 5
For more info please call Sam Murphy on 0044 208 544 3423 / sam.murphy@tecgroup.net
Global Regulatory Affairs CMC, Manager
Richmond, VA
Apr 4
I manage a range of other permanent and freelance positions for a broad portfolio of clients, so if the above role isn’t for you but you’d nevertheless like to discuss other opportunities currently available both now and in the near future, we are happy to get in touch at your discretion. Contact Ross Apted at (646) 586 9087 today!
Clinical Development Manager - Geneva
Switzerland
Apr 3
Clinical Development
Statistician / Senior Statistician (Contract or Permanent)
San Diego
Apr 3
For more information on this position please contact Sam Murphy via sam.murphy@tecgroup.net / 0044 (0) 208 544 3423
Director, Global Regulatory Affairs; Immuno-Oncology
Boston MA
Apr 3
Tec Group international has partnered with a global Pharmaceutical company to find a regulatory profile to help lead the business and Regulatory departments. This position offers a creative platform for the chosen candidate to work on projects and areas they excel in. This position is based in Boston and offer a competitive salary and package. For more info please contact Sam Murphy at TEC Group sam.murphy@tecgroup.net
Associate Director, Global Regulatory Affairs; Immuno-Oncology
USA
Apr 3
For more info please call Sam Murphy on 0044 208 544 3423 / sam.murphy@tecgroup.net
Senior Manager, Global Regulatory Affairs
New Jersey
Apr 3
I manage a range of other permanent and freelance positions for a broad portfolio of clients, so if the above role isn’t for you but you’d nevertheless like to discuss other opportunities currently available both now and in the near future, we are happy to get in touch at your discretion. Contact Ross Apted at (646) 586 9087 today!
ASSOCIATE DIRECTOR/DIRECTOR REGULATORY AFFAIRS (DEVELOPMENT)
New Jersey
Apr 3
I manage a range of other permanent and freelance positions for a broad portfolio of clients, so if the above role isn’t for you but you’d nevertheless like to discuss other opportunities currently available both now and in the near future, we are happy to get in touch at your discretion. Contact Ross Apted at (646) 586 9087 today!
Associate Director, Regulatory Affairs CMC
Edison, NJ
Apr 3
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.
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