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The latest Regulatory jobs

Jobs: (Regulatory)

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Proposal Specialist (Regulatory)
Bucharest, Bucure ti,Romania
Jan 20
Job Purpose:A junior regulatory professional who utilizes principles and standards to (a) support the development of high quality proposals, budgets, and other related documentation within agreed priorities and time scales and (b) manage and maintain resources, processes, and databases. ...
Head of Medical Regulatory and Public Affairs
England
Jan 20
As Head of Medical, Regulatory and Public Affairs you are responsible for leading and developing our Medical and Public Affairs strategy, to ensure we meet the Regulatory requirements for the UK and Ireland whilst also leading the overall company Quality Management. ...
Principal Regulatory Writer
Chicago
Jan 19
One of the leading companies in Pharmaceuticals is in search for a talented Principal Regulatory Writer to support their Immunology and Oncology teams. This is...
Associate Director Regulatory Affairs
England
Jan 19
Avni Bhayani at Umbilical Life is recruiting a permanent experienced Associate Director Regulatory Affairs EU/ROW for an expanding pharmaceutical company based in London. The associates director will provide regulatory oversight/ leadership to this key business process; providing strategic direction and regulatory review for commercial activities for the EU/ROW markets; interacting with Health Authorities and assisting with managing responses to inquiries if required.
Associate Director, Regulatory Affairs - Medical Devices
Chippenham or Cambridge
Jan 19
If you are an expert in Medical Device regulatory affairs and want to be part of a team that transforms the lives of airways disease patients then Vectura is very keen to hear from you.
Regulatory Affairs CMC Manager Freelance
Germany
Jan 19
Für unseren Kunden sind wir aktuell auf der Suche nach einem Freelance Regulatory Affairs CMC Manager (m/w). ...
Director of Regulatory CMC
London
Jan 19
Director of Regulatory CMC - LondonJOB SUMMARY: i-Pharm Regulatory are recruiting for a Director of Regulatory for a very well respected niche Biotech based in Central London. If you’re an experienced Regulatory Affairs Associate Director/Director with deep knowledge in CMC along with commercial experience with an FDA/EMA approved drug products then this is the job for you.Candidates must be eligible to work in the UK. ...
Regulatory Submissions (Study Start-up) Manager
Germany
Jan 19
Regulatory Submissions (Study Start-up) Manager Our client is a global, full-service Clinical Research Organization (CRO) specializing in a multitude of therapeutic areas. They are active in over 45 countries across the globe. They continue to steadily grow and are looking to add to their team! Their clinical operations activities are growing rapidly, and we are currently seeking a full-time, office-based Regulatory Submissions Manager to join our Clinical Operations team. ...
Head of Regulatory
Frankfurt am Main
Jan 19
Regulatory Head    A leading Pharmaceutical manufacturing company is seeking an experienced Regulatory Head required in Frankfurt. The Regulatory Head will be responsible for the Full...
Regulatory Affairs Associate- Clinical Trials
Czech Republic
Jan 19
Regulatory Affairs Associate- Prague/Czecz Republic!A Regulatory Affairs Associate needed for one of the leading CRO companies in Prague.If you are an experienced professional within regulatory affairs for Clinical Trials and you would like to develop your career with world- leading company, do not hesitate to apply just now.
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Manager (m/w) Regulatory Affairs CMC
München
Jan 19
Manager (m/w) Regulatory Affairs CMCIn München / Vollzeit, unbefristetIhre Aufgaben:- Betreuung der operativen Aufgaben für den Bereich Regulatory Affairs CMC im Rahmen der Zusammenarbeit mit anderen Abteilungen, Ihren Regulatory Affairs Kollegen, sowie externe Partner und Hersteller- Die Erstellung diverser CMC/Qualitätsrelevante Dokumente, wie z.B. die Qualitätsteile des IMPD, IND und des CTD (Modul 2.3 und 3). ...
Regulatory Labeling Operations and Compliance Manager
London
Jan 19
An international Pharmaceutical, with their HQ in London, UK are looking for a Labeling Operations and Compliance Manager to be the subject matter expert on labeling process and compliance. You will be accountable for process improvement to support inspection readiness, management of the EU linguistic process, readability requirements and packaging & labeling review. Naturally, in this position you will be a collaborating with commercial, supply chain, legal, safety, medical and others.
OPTION BELGIQUE Sr / Regulatory Programme Manager EU and GRL Career Pathway No mature products GAIN RA Dev and NEW Lifecycle
Belgium
Jan 19
This role will appeal to individuals who want to work in a Global HQ where 70% of ALL decisions are made in the same building! This role is based in Belgium, comes with an attractive salary, bonus, and a great deal of opportunity to grow. This company has a track record of developing individuals from Manager and Senior to the Global Regulatory Lead level!
M4 CORRIDOR Regulatory Programme Manager EU and GRL Career Pathway NMEs and Lifecycle combined Pure mAbs role
M4 Corridor
Jan 19
This role will appeal to individuals working in US companies where decision making is sometimes held back in the US, and you want to be in a company where 70% of ALL decisions are made in the EU. This role can be based in the M4 Corridor / West of London, Middlesex & Berks areas, come with an attractive salary, bonus, and a great deal of opportunity to grow. This company has a track record of developing individuals from Manager and Senior to the Global Regulatory Lead level.
Regulatory Medical Writer
UK Wide
Jan 19
Regulatory Medical Writer This internationally recognised pharmaceutical firm seeks an experienced Regulatory Medical writer to join their established team on a fully remote basis.
Regulatory Affairs Manager – AdPromo
Cambridge, MA
Jan 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!
Senior Regulatory Executive - Middlesex
Middlesex
Jan 19
Mary Bolt is recruiting for a Senior Regulatory Executive to join a science-led, global healthcare company at their site based in Middlesex on a 12...
Regulatory Initiative Project Manager - Hertfordshire
Hertfordshire
Jan 19
Mary Bolt is recruiting for a Regulatory Initiative Project Manager to join a research-focused healthcare company at their site based in Hertfordshire on a contract...
Senior Regulatory Consultant - Buckinghamshire
Buckinghamshire
Jan 19
Mary Bolt is recruiting for a Senior Regulatory Consultant to join a highly established research-based pharmaceutical company at their site in Buckinghamshire. This position is...
Regulatory Affairs Manager
Tadworth
Jan 18
Here is an exciting pharmaceutical job one of the industry's most prestigious organisations. There is a vacancy for a Regulatory Affairs Manager to join a global top 10 pharmaceutical company at their offices located in Surrey. This role will work with internal PEH groups and relevant project teams to support on-market biosimilars. ...
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Regulatory Consultant
Tadworth
Jan 18
Here is an exciting pharmaceutical job one of the industry's most prestigious organisations. There is a vacancy for a Regulatory Consultant to join a global top 10 pharmaceutical company at their offices located in Surrey. This role will allow the company to legally study, manufacture, market and supply medicines. To obtain, manage and maintain product Marketing Authorisations and Clinical Trial Authorisations (where applicable) in line with business goals and legal requirements. ...
Regulatory Affairs Specialist- Clinical Trials
Prague
Jan 18
Regulatory Affairs within Clinical Trials required for one of TOP 10 CRO based in Czech Republic. We are looking for candidate for full time position. You would be responsible for Global regulatory Affairs. Please apply ASAP to find out more!
Regulatory Project Manager
New South Wales
Jan 18
Sydney based market-leading Medical Device company require a Regulatory Affairs Product Manager to help the organisation with RA for new and existing markets. On offer is a competitive salary, guaranteed bonus, super and other benefits.
Regulatory Affairs Manager - Some remote working and flexible hours.Great variety of work and work for a company that is different.
Oxfordshire
Jan 18
To apply for this regulatory affairs role please call Julie Cooper on 07951 082482 or send your CV to: julie@mosaicrecruitment.co.uk
Regulatory Affairs Compliance Manager -EU and US Cosmetics role - will consider Consumer , Food Supplements or Medical Devices background
Nottingham
Jan 18
To apply for this regulatory affairs role please call Julie Cooper on 07951 082482. Alternatively please send your CV to:julie@mosaicrecruitment.co.uk
Senior Regulatory Affairs Associate
Slough
Jan 18
At Lonza, we invest in great people. We encourage our employees to challenge themselves and we offer an environment that fosters creativity and success. Headquartered in Basel, Switzerland, we operate production, R&D, and business sites around the world, including Europe, North America, and Asia. Our vision: We strive to be the leading supplier using science and technology to improve the quality of life. ...
Regulatory Affairs Manager
homebased/Reading
Jan 18
PURPOSE Manages a regulatory and/or technical project, for both internal and external clients, as appropriate. Provides strategic regulatory and/or technical consultancy on a variety of projects.  RESPONSIBILITIES Acts as a Lead Regulatory Professional on any type of writing or technical project, with limited guidance from senior staff using experience and initiative to generate new and unusual document types to meet customer requirements. ...
Senior Regulatory Associate CTA
Cambridge
Jan 18
Senior Regulatory Associate - Development My client, a leading Regulatory Affairs consultancy, is looking for Regulatory candidate with a good background in compiling and submitting CTA's to join their development team as a Senior Regulatory Associate focusing on EU submissions. This role might suit an Associate looking to take the next step in their career. You will be working with some really exciting clients and have direct responsibility for EU CTA submissions. ...
Regulatory Manager (Animal Health)
IL, USA
Jan 18
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!
Drug Regulatory Affairs Manager (m/w)
Germany
Jan 18
Freelance Office-Based SüddeutschlandAufgaben:• Eigenverantwortliche Planung und Durchführung von regulatorischen Projekten • Treffen projektbezogener Entscheidungen, Koordination und Management von regulatorischen Projektteams sowie Projektsteuerung und –reporting • Anstoß und Verfolgung von Neueinrichtungsprojekten, Terminüberwachung und Priorisierung von regulatorischen Aktivitäten • Mitarbeit an strategisch regulatorischen Fragestellungen im internationalen Umfeld • Erste ...
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Senior Manager Regulatory Affairs
London
Jan 18
My client is an established pharma who are growing their Regulatory Affairs function in their London based office. They now require a Senior Manager experienced with CTA activities and pre-submissions to manage a successfully marketed product. Please read on and click apply to make an application!
Regulatory Affairs Associate Director-144043
Europe, Middle East and Africa-UK-England-Cambridge,
Jan 18
  PPD Regulatory Affairs department has an exciting new career opportunity available.   The purpose of this role is to provide innovative solutions including global regulatory therapeutic area expertise and client interface to provide strategic regulatory intelligence, guidance and regulatory expertise for product development from preclinical through registration and product optimization. ...
Senior Regulatory Affairs Specialist - EMEA role - must have medical devices experience
Midlands
Jan 17
To apply for this regulatory affairs medical devices role please call Julie Cooper on 07951 082482 or send your CV in the strictest confidence to :julie@mosaicrecruitment.co.uk
Director of Regulatory CMC
London
Jan 17
Director of Regulatory CMC - LondonJOB SUMMARY: i-Pharm Regulatory are recruiting for a Director of Regulatory for a very well respected niche Biotech based in Central London. If you’re an experienced Regulatory Affairs Associate Director/Director with deep knowledge in CMC along with commercial experience with an FDA/EMA approved drug products then this is the job for you.Candidates must be eligible to work in the UK. ...
Associate Director Regulatory Affairs
London
Jan 17
Associate Director of Regulatory Affairs – London JOB SUMMARY: i-Pharm Regulatory are recruiting for an Associate Director of Regulatory for a very well respected niche Biotech based in Central London. The purpose of this role is primarily focused on leading an MAA for an Orphan Drug (ATMP) and supporting the expanding portfolio of development molecules and delivering on European Regulatory strategy.Candidates must be eligible to work in the UK. ...
Senior Regulatory Affairs Associate
Slough
Jan 17
At Lonza, we invest in great people. We encourage our employees to challenge themselves and we offer an environment that fosters creativity and success. Headquartered in Basel, Switzerland, we operate production, R&D, and business sites around the world, including Europe, North America, and Asia. Our vision: We strive to be the leading supplier using science and technology to improve the quality of life. ...
Regulatory Affairs
Rep. Ireland
Jan 17
We are recruiting for a number of Regulatory Affairs vacancies with our clients in the Pharmaceutical and Medical Device industries.
Senior Regulatory Affairs Specialist
Rep. Ireland
Jan 17
My client is an international pharmaceutical company with offices in Dublin. We are currently recruiting on their behalf for a Senior Regulatory Affairs Specialist. 
Senior Regulatory Affairs Specialist
ClujNapoca
Jan 17
Senior Regulatory Affairs Specialist:A dynamic Medical Device company is seeking a Senior Regulatory Affairs Specialist for their developing site in Romania. The Specialist will...
Senior Regulatory Consultant
Cambridgeshire
Jan 17
Senior Regulatory Consultant Regulatory Professionals are collaborating with an established consultancy based in Cambridgeshire who are looking to expand their team.
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Regulatory Affairs Manager
Buckinghamshire
Jan 17
Regulatory Affairs Manager We are collaborating with a Top 10 Global Pharmaceutical company based in Buckinghamshire who are recruiting for here next talented Regulatory Affairs Manager.
Director, Regulatory Affairs
London
Jan 17
A global Regulatory Affairs consultancy is currently looking for a Regulatory Leader to join their expanding Regulatory Affairs team. This position has arisen due to an influx of projects working with ATMP products in development. Within this position you would be principally accountable for Regulatory project management and client engagement. You will be based within the European headquarters in Paris, France / London, UK / Lausanne, Switzerland.
Global Regulatory Lead
Brussels
Jan 17
A large Pharmaceutical company is currently looking for a Regulatory professional to join their lean Regulatory Affairs team. This position has arisen due to an progression of key products through the development pipeline. Within this position you would be principally accountable for Global Regulatory project management and submissions. You will be based within the European headquarters in Brussels, Belgium. Ideally you will have exposure to working with Gene Therapy products in development.
Senior Regulatory Project Lead
Geneva
Jan 17
An innovative Biopharmaceutical company is currently looking for a Senior Leader to join their Global Regulatory Affairs team. This position has arisen due to an increased workload moving forward in global projects, submissions and development pipeline. Within this position you would be principally accountable for Global Regulatory project management, competent authority negotiation, strategy development and implementation.
Global Regulatory Affairs Officer
Rep. Ireland
Jan 17
Ideal new position for a Regulatory Affairs professional looking to gain global experience.
Regulatory Affairs Manager
Buckinghamshire
Jan 17
Regulatory Professionals are working with a well-established, global Pharmaceutical company based in Buckinghamshire. This client is looking for a Regulatory Affairs Manager to predominantly work on their MAA post approval activities to also assist with any drug development duties required.
Regulatory Affairs Manager (m/w) für Medizinprodukte Schweiz
Switzerland
Jan 17
Für unseren Kunden, ein innovates medical device Unternehmen in der Schweiz, sind wir aktuell auf der Suche nach einem Regulatory Affairs Manager (m/w) für Medizinprodukte. ...
Regulatory Affairs Medical Writer
Germany
Jan 17
Aufgaben:• Vorbereitung und Erstellung der Regulatory Affairs Dokumentation• Unterstützung und Beratung von allen Aspekten der Medical Writing in jeder Phase des Entwicklungsprozesses• Erstellung von Clinical Study Reports, MAAs, CTAs, Investigator’s Brochures sowie weiteren Zusammenfassungen und Dokumenten gemäß den internationalen RichtlinienVoraussetzungen:• Abgeschlossenes Studium oder eine vergleichbare Ausbildung• Mindestens 3 Jahre Erfahrung in Medical Writing• Gute Or ...
Regulatory/ Study-Start up Specialist,- Reading/Slough - Up to £40K 
UK, Reading, Berkshire
Jan 16
Regulatory/ Study-Start up Specialist,- Reading/Slough - Up to £40K  We are currently recruiting for a highly recognised CRO that are growing their study start-up team as a core function. This is a great time to join this team as it is set to grow and develop rapidly in the future. Please contact Zoe Benningfield-Fox on 0203 019 6022 or email zoe@peoplewithchemistry.com
Senior Regulatory Process Manager
Belgium
Jan 16
Regulatory trainer - Belgium - Freelancing
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CMC Regulatory Writer
Belgium
Jan 16
CMC - Regulatory Technical Writer
Principle Regulatory Executive
Middlesex
Jan 16
My Client a Global Pharmaceutical Company has opened a new vacancy within their Regulatory team and are looking to recruit a Principal Regulatory Affairs Executive - to be based at their offices in Middlesex on an initial 6 month contract.
Regulatory Consultant - Biologics
Berkshire
Jan 16
Regulatory Consultant - Biologics This internationally recognised pharmaceutical organisation seeks an experienced Regulatory Consultant to join their established team focusing specifically within Biologics.
Senior Regulatory Affairs Officer Submissions
Dublin, Republic of Ireland
Jan 16
Our client, a global pharmaceutical company, are currently recruiting for a Senior Regulatory Affairs Officer Submissions
EMEA Regulatory Liaison
Buckinghamshire
Jan 16
Regulatory Liaison - EMEA A globally recognised pharmaceutical firm based in Buckinghamshire seeks an Regulatory Affairs Liaison with extensive knowledge of EMEA regions.
Regulatory Affairs Executive
Cambridgeshire
Jan 16
Regulatory Affairs Executive Regulatory Professionals are collaborating with an established consultancy based in Cambridgeshire who are looking to expand their team.
Senior Regulatory Consultant
Cambridgeshire
Jan 16
Senior Regulatory Consultant Regulatory Professionals are collaborating with an established consultancy based in Cambridgeshire who are looking to expand their team.
Regulatory Affairs Gruppenleiter (m/w)
Bern
Jan 16
Gruppenleiter (m/w) Regulatory Affairs ClinicalUnbefristete Vollzeitstelle in Deutschland/der Schweiz zu besetzenIhre Aufgaben:- Führung eines Teams spezialisiert auf die operative Realisierung der Clinical Trial Applications, mit Berücksichtigung der Firmenvorgaben, regulatorischen Anforderungen, Timelines und des Budgets- Pflege auf Aufbau der Prozesse, Verfahren und Systeme zur Unterstützung des globalen CTA Managements- Überwachung der externen Dienstleister um die sicherzustellen dass d ...
Regulatory Affairs Manager (Biosimilars) contract
Berkshire
Jan 16
Minimum 6 month contract for a regulatory professional with biologics experience ideally spanning the product lifecycle. Biosimilars experience preferred but not essential.
Regulatory Affairs Director
San Francisco, CA
Jan 16
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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Associate Director, Regulatory Affairs – Advertising and Promotion
Boston, MA
Jan 16
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!
Regulatory Affairs Specialist
Heidelberg
Jan 16
Regulatory Affairs Specialist Based in the beautiful city of Heidelberg, a leading medical device group of companies are currently recruiting a Regulatory Affairs specialists to join their team.
Regulatory Biologics Consultant
Berkshire
Jan 16
My Client a Global Pharmaceutical Company has opened a new vacancy and is looking to recruit a Regulatory Biologics Consultant on an initial 6 Month contract to be based at their offices in Berkshire.
Regulatory Affairs Manager - Medical Devices
Berlin
Jan 16
**Cardiovascular Medical Device Opportunity**ewi Life Sciences are excited to be partnering with a leading cardiovascular medical device company based in Germany.Our client are currently looking for a Regulatory Affairs Manager who has around 3-5 years experience and has a background in R&D and strong Project Management skills. ...
Regulatory Affairs Manager (m/w) für Medizinprodukte
Bayern
Jan 16
Role / Description:Our client a market leading company within the medical device market in Bavaria is urgently looking for Regulatory Affairs Manager (m/w) that can help them with the new regulations for medical devices. ...
Regulatory Affairs Specialist (m/w)
Germany
Jan 16
Aufgaben:• Enge Zusammenarbeit mit der Entwicklungs- und Vertriebsabteilung• Erarbeitung von Zulassungsvoraussetzungen auf internationaler Ebene• Erstellung und Prüfung von Zulassungsdokumenten für die Registrierung, Änderungsanzeigen und die Zulassungsverlängerungen• Einreichung der Zulassungsunterlagen bei den jeweiligen Länderbehörden, um den Verkauf der Produkte in den internationalen Märkten zu gewährleisten• Entwicklung von Produktzulassungsstrategien in Zusammenarbeit mit den Vertrieb ...
Regulatory Affairs Specialist (w/m) in Graubünden
Graubünden
Jan 16
Regulatory Affairs Specialist (w/m) in GraubündenUnser Kunde ist weltweit bekannt für die Bedienfreundlichkeit sowie die intelligente und automatische Anpassung der Medizinproduktewelt an die Bedürfnisse der Patienten. Unser Kunde entwickelt und produziert Medizintechnikgeräte in der Schweiz und vermarkten diese weltweit. ...
Regulatory Affairs Manager x 2 - International role- Cosmetics - all regulatory experience considered
Nottingham
Jan 15
To apply for this regulatory affairs role please call Julie Cooper on 07951 082482. Alternatively please send your CV to:julie@mosaicrecruitment.co.uk
Senior Regulatory Affairs Specialist - EMEA role - must have medical devices experience- 1 or 2 days remote working after probation period.
Midlands
Jan 15
To apply for this regulatory affairs medical devices role please call Julie Cooper on 07951 082482 or send your CV in the strictest confidence to :julie@mosaicrecruitment.co.uk
Regulatory Affairs Manager - Some remote working and flexible hours.Great variety of work and work for a company that is different.
Oxfordshire
Jan 15
To apply for this regulatory affairs role please call Julie Cooper on 07951 082482 or send your CV to: julie@mosaicrecruitment.co.uk
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Regulatory Affairs Manager - International role- Cosmetics - Food supplements and medical devices experience considered
Nottingham
Jan 15
To apply for this regulatory affairs role please call Julie Cooper on 07951 082482. Alternatively please send your CV to:julie@mosaicrecruitment.co.uk
Senior Regulatory Affairs Specialist - EMEA role - must have medical devices experience
Midlands
Jan 15
To apply for this regulatory affairs medical devices role please call Julie Cooper on 07951 082482 or send your CV in the strictest confidence to :julie@mosaicrecruitment.co.uk
Leitung Regulatory Affairs and Quality Management (m/w)
Stuttgart
Jan 15
Leitung Regulatory Affairs & Quality Management (m/w)Aufgaben:- Disziplinarische Leitung der Abteilungen QM & RA- Schnittstelle zwischen Entwicklung, Produktion und Marketing- Erstellung von Strategien für das Qualitätsmanagement und Sicherstellung der Ziele- Weiterentwicklung und Optimierung des QMS gemäß marktüblicher regulatorischer Vorgaben- verantwortlicher QMB- verantwortlich für die Durchführung interner und externer Audits- Ansprechpartner für benannte Stellen und Behörden- Verantwor ...
Regulatory Submissions (Study Start-up) Manager
London
Jan 15
POSITION SUMMARYMedpace is a global, full-service Clinical Research Organization (CRO) specializing in a multitude of therapeutic areas. Our headquarters are located in Cincinnati, Ohio and we are active in over 40 countries across the globe. We continue to steadily grow and are looking to add to our team! Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, office-based Regulatory Submissions Manager to join our Clinical Operations team. ...
Senior Regulatory Submissions Coordinator
Russia
Jan 15
A top quality provider and global CRO is currently seeking a Senior Regulatory Submissions Coordinator to join their team. You will play a key role in the management process for study start up and clinical trials by managing start-up of projects while being provided with training to ensure career progression. This is a full-time permanent position home-based in Moscow.
Regulatory Submissions Coordinator
England
Jan 15
A top quality provider and global CRO is currently seeking a Regulatory Submissions Coordinator to join their team. You will play a key role in the management process for study start up and clinical trials by managing start-up of projects while being provided with training to ensure career progression. This is a full-time permanent position based in London, UK.
Regulatory Operations Associate
Uxbridge
Jan 15
An exciting opportunity has arisen for a Regulatory Operations Associate to join a global biopharmaceutical company based in West London. A very patient-focused company, who scientific research has resulted in 15 marketed products that are benefitting hundreds of thousands of people, a pipeline of late-stage drug candidates and unmatched patient access programs to ensure medications are available to those who could otherwise not afford them. ...
Regulatory Submissions Manager, Study Start-Up
Italy
Jan 15
A top quality provider and global CRO is currently seeking a Regulatory Submissions Specialist to join their team. You will play a key role in the management process for study start up and clinical trials by managing start-up of projects while being provided with training to ensure career progression. This is a full-time permanent position based in Milan, Italy.
Regulatory Submissions (Study Start-Up) Specialist
Sweden
Jan 15
A top quality provider and global CRO is currently seeking a Regulatory Submissions Specialist to join their team. You will play a key role in the management process for study start up and clinical trials by managing start-up of projects while being provided with training to ensure career progression. This is a full-time permanent position based in either Sweden, Denmark or Finland.
(Senior) Manager Regulatory Affairs
England
Jan 15
A major global research-driven pharmaceutical company is seeking a Manager Regulatory Affairs to join their team. You will be responsible for providing guidance and support on the submission strategy regarding EU regulations and working closely with project teams in Japan and US too. You will provide expertise across a range of regulatory requirements around Europe with the opportunity for career development. This is a full-time permanent position based in London, UK.
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Regulatory Affairs Team Leader - Spain
Madrid
Jan 15
ProClinical is working with a specialist pharmaceutical organisation with a rich history of developing innovative products to improve the quality of patient lives within areas of key medical need. At this time they are seeking a team leader to manage a team of professionals of varying career levels as well as lead registration procedures for new and existing products. ...
Regulatory Affairs Manager (m/w) für Medizinprodukte
Bayern
Jan 15
Für unseren Kunden, ein innovates medical device Unternehmen in Bayern, sind wir aktuell auf der Suche nach einem Regulatory Affairs Manager (m/w) für Medizinprodukte. ...
Senior Regulatory Medical Writer
Uxbridge, England,United Kingdom
Jan 13
Write clinical documents for submission to regulatory authorities, including but not limited to: briefing documents, clinical development plans, previous human experience summaries, human pharmacology summaries, investigator brochures, study protocols, model informed consents, interim and final clinical study reports, common technical document (CTD) clinical overviews and summaries, safety update/aggregate reports, integrated summaries of safety and efficacy. ...
Senior Regulatory Medical Writer
Uxbridge, England,United Kingdom
Jan 13
This position is open for applicants from UK and Spain. ...
Senior Regulatory Medical Writer
Uxbridge, England,United Kingdom
Jan 13
Role: Senior Medical WriterLocation: UK, UxbridgeSalary: CompetitivePosted on: 22 Dec 2017Closing date: 19 Jan 2018The Senior Medical Writer researches, creates, and edits all documents associated with clinical research. Responsibilities also include: acting as primary client contact for medical writing projects, working with other PAREXEL departments and clients to set and meet internal and external deliverable timelines, leadership, training and support of junior medical writing staff. ...
Senior Regulatory Medical Writer
Uxbridge, England,United Kingdom
Jan 13
This position is open for applicants from UK and Spain. ...
Senior Regulatory Medical Writer
Uxbridge, England,United Kingdom
Jan 13
This position is open for applicants from UK and Spain. ...
Regulatory Affairs - Associate Director
England
Jan 12
Avni Bhayani at Umbilical Life is recruiting a permanent experienced Associate Director Regulatory Affairs EU/ROW for an expanding pharmaceutical company based in London. The associates director will provide regulatory oversight/ leadership to this key business process; providing strategic direction and regulatory review for commercial activities for the EU/ROW markets; interacting with Health Authorities and assisting with managing responses to inquiries if required.
Senior Regulatory Affairs Consultant (m/w) CMC
München
Jan 12
Senior CMC Consultant (m/w) Regulatory AffairsOffice-based in Munich, full-timeIhre Aufgaben:- Die Beratung internationaler Pharmaunternehmen auf globaler Ebene, mit Fokus auf EU und den USA- Projektsteuerung und Bearbeitung regulatorischer Projekte in allen Phasen der Entwicklung, von der frühen Entwicklung bis hin zur Marktzulassung in allen Indikationen, überwiegend im Bereich Biotechnologie- Ansprechpartner und Subject Matter Expert für den Bereich CMC Regulatory Affairs gegenüber Behörd ...
Spezialist technische Dokumentation und Regulatory Med Dev
Frankfurt am Main
Jan 12
Spezialist technische Dokumentation und Regulatory in der Medizintechnik (m/w)Office-based in Frankfurt - vollzeit, unbefristetAufgaben:- Überarbeitung von Produktakten mit dem Schwerpunkt auf Risikomanagement, Usability und electrical Safety- Aufbauplanung der technischen Dokumentation- Einreichung der Produktakten bei den zuständigen Behörden- Optimierung des QM- System nach entsprechenden Normen- Überarbeitung von Reklamationen der benannten Stellen Voraussetzungen:- Abg ...
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Regulatory Affairs Associate
Germany
Jan 12
A top quality provider and global CRO is currently seeking a Regulatory Affairs Associate to join their team You will play a key role in the management process for study start up and clinical trials by advancing the start-up of projects and negotiating contracts and budgets while being provided with training to ensure career progression This is a full time permanent position with competitive salary and extensive package based in Munich, Germany.
Senior SSU and Regulatory Specialist (Bulgaria)
Bulgaria
Jan 12
Why Syneos Health? Join a game-changing company that is reinventing the way therapies are developed and commercialized. Created through the merger of two industry leading companies, INC Research and inVentiv Health, we bring together more than 22,000 clinical and commercial minds to create a better, smarter, faster way to get biopharmaceutical therapies into the hands of patients who need them most.
Senior SSU and Regulatory Specialist (Bulgaria)
Bulgaria
Jan 12
Why Syneos Health? Join a game-changing company that is reinventing the way therapies are developed and commercialized. Created through the merger of two industry leading companies, INC Research and inVentiv Health, we bring together more than 22,000 clinical and commercial minds to create a better, smarter, faster way to get biopharmaceutical therapies into the hands of patients who need them most.
Regulatory Affairs Associate
Germany
Jan 12
A top quality provider and global CRO is currently seeking a Regulatory Affairs Asociate to join their team You will be working in the Global Regulatory department and will be a key member in the preparation and delivery of regulatory submissions. Training is also provided to enhance career development and progression. This is a permanent position with competitive salary and extensive benefits package based in Munich, Germany.
Regulatory Affairs Expert (m/w)
Baden-Württemberg
Jan 12
Regulatory Affairs Expert (m/w)Office-based in Baden- WürttembergAufgaben:- Erstellung der technischen Dokumentation für die Zulassung von Medizinprodukten- Prüfung und Überarbeitung der Anforderungen der regulatorischen Vorgaben - Kommunikation mit den zuständigen Behörden - Einreichung der Dokumente- Durchführung interner Audits- Ansprechpartner in allen zulassungsspezifischen Fragen für die angrenzenden Fachbereiche- Entwicklung von ZulassungsstrategienVoraussetzungen:- Studium mit techni ...
Regulatory Submissions Manager (m/w), office-based in Munich
München (81249)
Jan 12
Regulatory Submissions (Study Start-up) Manager Our client is a global, full-service Clinical Research Organization (CRO) specializing in a multitude of therapeutic areas. They are active in over 45 countries across the globe. They continue to steadily grow and are looking to add to their team! Their clinical operations activities are growing rapidly, and we are currently seeking a full-time, office-based Regulatory Submissions Manager to join our Clinical Operations team. ...
Regulatory Submissions (Study Start-up) Manager (m/w)
Germany
Jan 12
Regulatory Submissions (Study Start-up) Manager Our client is a global, full-service Clinical Research Organization (CRO) specializing in a multitude of therapeutic areas. They are active in over 45 countries across the globe. They continue to steadily grow and are looking to add to their team! Their clinical operations activities are growing rapidly, and we are currently seeking a full-time, office-based Regulatory Submissions Manager to join our Clinical Operations team. ...
Director of Regulatory Affairs, Medical Device
Netherlands
Jan 12
A top quality provider and global CRO is currently seeking a Director of Regulatory Affairs to join their device team. You will be responsible for the oversight of the process and activities that will ensure company’s success related to product submissions as well as develop global strategies in collaboration with international regulatory agencies. This is a permanent positive based in either Maastrich, Netherlands or Munich, Germany.
Senior Regulatory Affairs Specialist - Medical Devices
Switzerland
Jan 12
Senior Regulatory Affairs Specialist - Medical Devices - Class III
Regulatory CTA Submission Consultant
Surrey
Jan 12
My Client a Global Pharmaceutical Company has opened a new vacancy within their Regulatory team and is looking to recruit a Regulatory CTA Submission Consultant on an initial 6 Month rolling contract to be based at their offices in Surrey
regulatory jobs : 100 +
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