Associate Director of Regulatory Affairs Associate Director of Regulatory Affairs -- San Francisco Bay Area Our Client is a clinical-stage pharmaceutical company engaged in discovering and developing novel therapeutic RNAi drug candidates. The Company has a fully integrated drug development platform that spans therapeutic target identification to drug development. Job Description The Associate Director will provide expertise in translati ...[more]
Career Level:
Manager (Manager/Supervisor of Staff)
Medical Staffing Allied
San Francisco, CA
Jul 3
Medical Project Manager Medical Project Manager Overview Our client is a leading international clinical research organization (CRO) with proven expertise in supporting global clinical trials for pharmaceutical, biotechnology and medical device companies. Well-designed trials span the product development lifecycle from first-in-man through regulatory approval and post-marketing surveillance studies. Major therapeutic cate ...[more]
Career Level:
Manager (Manager/Supervisor of Staff)
Salary:
75,000.00 USD per hour
Medical Staffing Allied
Southborough, MA
Jul 3
Compliance and Regulatory Affairs Manager UK mBlox is the world’s largest mobile transaction network. Specialising in the commercial and technical complexities of mobile payment and message transmission, mBlox is in the business of connecting companies with customers. The result of this dedicated attention to messaging services is that mBlox delivers comprehensive and reliable SMS transport and financial settlement services. With an internat ...[more]
Job Type:
Employee
Job Status:
Full Time
mBlox Ltd
London, London
Jul 3
Human Resources Manager (m/f) Welcome to Mundipharma Research! Mundipharma Research belongs to a group of independent associated companies undertaking international R&D activities with a main focus on the therapeutic fields of pain, oncology and respiratory diseases. Within Europe, Mundipharma Research has two joint units in Germany and the UK which provide services with regard to Preclinical and Clinical Development, Pharmace ...[more]
Career Level:
Manager (Manager/Supervisor of Staff)
Job Type:
Employee
Job Status:
Full Time
Mundipharma Research GmbH & Co. KG
Limburg (Lahn), Hessen 65549
Jul 3
Manager, Regulatory Affairs - Promotional Manager Aspire to set new standards for excellence. A global specialty pharmaceutical and medication delivery company, Hospira is Advancing Wellness™ by discovering, developing, manufacturing, and marketing high-quality hospital products and technology solutions. We're among the leaders in our field, backed by decades of experience. We use unique methods to create dramatic results and we empower each empl ...[more]
Relevant Work Experience:
5+ to 7 Years
Career Level:
Manager (Manager/Supervisor of Staff)
Education Level:
Bachelor's Degree
Job Type:
Employee
Job Status:
Full Time
Hospira
Lake Forest, IL 60045
Jul 3
Pharmacovigilance Manager Summary - The Pharmacovigiliance Manager will act as national contact for pharacovigigiliance matters and be responsible for the following- * Enhancing and maintaining an efficient (PV) system in compliance with the national regulations for the UK * Ensuring appropriate contacts with Customer Services, Regulatory Affairs, QA, Medical Affairs, Clinical Research and other Business functions in the U ...[more]
Career Level:
Executive (SVP, VP, Department Head, etc)
Job Type:
Employee
Job Status:
Full Time
Salary:
80,000.00 GBP per year
Cooper Lomaz
Berkshire, HC
Jul 3
Associate Director of Marketing - Medical Devices Associate Director of Marketing Medical Devices The Associate Director of Marketing will have full responsibility for upstream and downstream marketing and is the manager of the development and implementation of marketing strategy and product development efforts. There will considerable interface with R&D, quality, regulatory affairs, and other functions within the organization as well as heavy in ...[more]
Relevant Work Experience:
10+ to 15 Years
Career Level:
Manager (Manager/Supervisor of Staff)
Education Level:
Bachelor's Degree
Job Type:
Employee
Job Status:
Full Time
Salary:
From 110,000.00 to 180,000.00 USD per year
MRINetwork
Atlanta, GA
Jul 3
Regulatory Affairs Associate REGULATORY AFFAIRS ASSOCIATE (SALARY: Negotiable) (BASED IN: HAMPSHIRE) Initially an 11 month contract for a regulatory affairs professional with not more than 3 years experience with regulaotry affairs. Key activities include:- • Provide regulatory support to the team, specifically with the transfer of documentation and marketing authorisation maintenance for 2009/2010 • Interpret applicable regu ...[more]
Job Type:
Temporary / Contract / Project
Job Status:
Full Time
Company Confidential
Job location not provided
Jul 3
Clinical Study Lead - Sponsor - international studies - lesen Sie mehr Warum auf diese Stelle bewerben? 1. Sie arbeiten bei einem globalen Pharmaunternehmen 2. Sie übernehmen Verantwortung in der Koordination von internationale Studien 3. Reiseanteil ist gering, da dies keine monitoring Stelle ist 4. Attraktive Bezahlung und Rahmenbedingungen 5. Unbefristete Stelle mit Sicherheit und Entwicklungsmöglichkeiten (vor allem in Clinical Project Management und Clinical Tea ...[more]
Career Level:
Experienced (Non-Manager)
Job Type:
Employee
Job Status:
Full Time
Progressive
SW Deutschland
Jul 3
Clinical Trial Manager - anspruchsvoll aber sehr interessant - Biotech Warum Bewerben? Ihre Vorteile: - Sie leiten eigenverantwortlich klinische Studien - Sehr attraktive Vergütung - Wachsen Sie mit der Firma und übernehmen Sie mehr Verantwortung - Sie sind maßgeblich für strategische Entscheidungen mitverantworlich - Sie können Ihr Wissen konkret umsetzen und sind nicht auf reine operative arbeit beschränkt - Offene und angenehme Team Atmosphäre Interesse an dieser n ...[more]
Career Level:
Experienced (Non-Manager)
Job Type:
Employee
Job Status:
Full Time
Progressive
SW Deutschland
Jul 3
Contract Regulatory Affairs Manager - 12 Months - Herts Leading Pharmaceutical company, situated in Hertfordshire are seeking a Regulatory Affairs Manager for a period of 12 months. My client are based in Hertfordshire and have a broad spectrum of products and Specialisms. They are a fantastic company to work for who have firm plans for UK expansion. Role Summary The ideal candidate will be responsible for the maintenance of the European Marketing Auth ...[more]
Career Level:
Experienced (Non-Manager)
Job Type:
Temporary / Contract / Project
Job Status:
Full Time
Paramount Recruitment Limited
Hertfordshire, HC AL00OO
Jul 3
Recruitment Consultant/Account Manager – Scientific – Cambridge Recruitment Consultant/Account Manager – Scientific – Cambridge The Benefits **Basic salary £18 – 25k, Negotiable, depending on experience **(Realistic OTE year 1 = £35k+, year 2, up to £50k **Uncapped commission, ( No threshold, for the 1st year!) **A superb opportunity, with a superb company! **Comprehensive REC approved training **Excellent benefits package The Client **A leading provider of to ...[more]
Relevant Work Experience:
2+ to 5 Years
Job Type:
Employee
Job Status:
Full Time
Salary:
From 18,000.00 to 25,000.00 GBP per year
Yes Rec2Rec
Cambridge, ANGL
Jul 3
Regulatory Affairs Manager (FMCG) Regulatory Affairs Manager (FMCG) (Budapest) Ref.sz.: 0002 Fizetés: Competitive On behalf of our international partner being present in the FMCG segment, we are looking to recruit an experienced Regulatory Affairs Manager to join the commercial office based in Budapest. Feladatok To lead and undertake all regulatory work necessary to meet the needs of the Company and in particular to be responsibl ...[more]
Career Level:
Manager (Manager/Supervisor of Staff)
Job Type:
Employee
Job Status:
Full Time
KARRIER HUNGĂRIA KFT.
Budapest
Jul 3
Clinical Managers Eidetica Biopharma GmbH is a young dynamic subsidiary of Biogen Idec – a global leader in the development, manufacture and commercialization of novel therapies within the fields of oncology and immunology. Founded in 2007 in Switzerland, Eidetica will develop and commercialize new therapeutic biopharmaceutical products with substantial commercial potential. We are seeking the following experts, wh ...[more]
Career Level:
Experienced (Non-Manager)
Job Type:
Employee
Job Status:
Full Time
Eidetica Biopharma GmbH
Zug, ZG 6300
Jul 3
Quality & Regulatory Affairs Manager (m/w) Wir vereinfachen Healthcare, indem wir uns auf die Menschen im Gesundheitswesen konzentrieren - auf Patienten und Anbieter. Wir suchen die beste Lösung für den Patienten. Und die wirtschaftlichste für das Gesundheitswesen. Unsere Produkte, Lösungen und Dienstleistungen orientieren sich an den wachsenden aber kostensensitiven Ansprüchen in unserem Gesundheitssystem – im Krankenhaus oder Zuhause. Pr ...[more]
Career Level:
Experienced (Non-Manager)
Education Level:
Bachelor's Degree
Job Type:
Employee
Job Status:
Full Time
Philips
Hamburg, Hamburg 20099
Jul 3
Regulatory Affairs Manager (m/w) - Zürich Regulatory Affairs Managers nutzen Sie diese einzigartige Chance, Teil eines erfolgreichen Unternehmens zu werden, in dem Sie noch weiter wachsen können. Starten Sie in einem krisensicheren Unternehmen mit sehr guten Partnern als: Regulatory Affairs Manager (m/w) - Zürich Lesen Sie auf welche Aufgaben Sie sich freuen können: - Strategieentwicklung und Zusammenstellung von Zulassungsdossiers zur Er ...[more]
Career Level:
Experienced (Non-Manager)
Job Type:
Employee
Job Status:
Full Time
Progressive
ZÜRICH
Jul 3
R&D Technical Assistant @ Orangina Schweppes International - Fantastic opportunity young graduates Orangina Schweppes International (OSI) Orangina Schweppes International is part of one of the largest soft drink producers in Europe, the Orangina Group. We are a major company, located in Amstelveen (Netherlands), in beverages whose quality brands and products are enjoyed around the world. The Orangina Group has a workforce of over 2,000 employees, sales volumes of 1.3 billion liters and a turnov ...[more]
Relevant Work Experience:
Less than 1 Year
Career Level:
Student
Education Level:
Bachelor's Degree
Job Type:
Employee, Temporary / Contract / Project, Intern
Job Status:
Full Time
Schweppes International Ltd
Amstelveen, NH 1183
Jul 3
Regulatory Affairs Manager - Nederland Zuid Het bedrijf maakt onderdeel uit van de grootste groep bedrijven met producten in de gezondheidszirg. In Nederland vindt heel veel onderzoek plaats met bestaande geneesmiddelen teneinde nieuwe toepassingen te vinden, maar ook om te leren van de ervaringen van patiënten en artsen die deze middelen in de dagelijkse praktijk gebruiken. Daarnaast heeft de organisatie in Nederland een belangrijk aandeel ...[more]
Career Level:
Experienced (Non-Manager)
Job Type:
Employee
Job Status:
Full Time
Real Resourcing
Tilburg
Jul 3
Director Global Submission Operations "Due to technical upgrades, this requisition is replacing requisition # 0903966. Any candidates who have already applied to requisition # 0903966 are already being considered, therefore, you do not need to apply". Johnson & Johnson Pharmaceutical Research & Development, LLC, a member of the Johnson & Johnson Family of Companies, is recruiting for a Director of Regulatory Global Submission Operatio ...[more]
Relevant Work Experience:
10+ to 15 Years
Career Level:
Executive (SVP, VP, Department Head, etc)
Education Level:
Bachelor's Degree
Job Type:
Employee
Job Status:
Full Time
Johnson & Johnson Family of Co
PA
Jul 3
Clinical Project Manager Contractor DESCRIPTIONS: The Clinical Project Manager in Global Clinical Trial Management will function as a Study Team Leader by organizing and managing all operational aspects of the study from conception to submission while ensuring adherence to timelines. The CPM will also proactively address risk management through contingency planning. The CPM will manage critical study issues such as budgeting, and dr ...[more]
Relevant Work Experience:
7+ to 10 Years
Career Level:
Manager (Manager/Supervisor of Staff)
Education Level:
Bachelor's Degree
Job Type:
Temporary / Contract / Project
Job Status:
Full Time
Salary:
From 50.00 to 55.00 USD per hour
Berman Larson Kane
Kenilworth, NJ 07033
Jul 3
Manager Quality Assurance & Regulatory Affairs (m/w) Präzisionssysteme für medizinische Anwendungen Manager Quality Assurance & Regulatory Affairs (m/w) Präzisionssysteme für medizinische Anwendungen Unser Klient ist ein international führender Hersteller innovativer Präzisionssysteme, die in naturwissenschaftlicher Forschung, Biotech- nologie und medizinischen Bereichen zur Anwendung kommen. Weltweit entwickelt und fertigt das Unternehmen High-Tech-Produkte, die höchsten Qualitätsstandards ents ...[more]
Career Level:
Manager (Manager/Supervisor of Staff)
Education Level:
Bachelor's Degree
Job Type:
Employee
Job Status:
Full Time
TOPOS Personalberatung GbR, Stuttgart
Hessen oder Baden-Württemberg
Jul 3
Senior Analyst Operations Controlling (m/w) Johnson & Johnson MEDICAL ist eine von drei erfolgreichen Sparten der mit rund 120.000 Mitarbeitern/ -innen weltweit führenden Johnson & Johnson Unternehmensfamilie. Wir leisten mit innovativen – oft richtungsweisenden – Medizintechnologien und -produkten einen wichtigen Beitrag zur erfolgreichen Behandlung einer Vielzahl weitverbreiteter und chronischer Krankheiten. Unterstützen Sie uns dabei! F ...[more]
Relevant Work Experience:
5+ to 7 Years
Career Level:
Experienced (Non-Manager)
Job Type:
Employee
Job Status:
Full Time
Johnson & Johnson MEDICAL GmbH
Norderstedt, Schleswig-Holstein 22851
Jul 3
Quality Engineer - Biotech Instrument Job Description: SUMMARY: Performs wide variety of professional Quality Engineering assignments of a various degrees of complexity under limited supervision with latitude for independent action and decision. Work involves the application of basic engineering principles to develop methods and procedures to improve and maintain product and process quality standards. Reports to the Manager, QA Regula ...[more]
Career Level:
Experienced (Non-Manager)
Job Type:
Employee
Job Status:
Full Time
Salary:
87,000.00 per year
At-Tech
San Jose, CA 95131
Jul 2
Manager of Clinical Data Management The Manager, Clinical Data Management will provide administrative and technical leadership to the clinical data management (CDM) group, through resource planning, scheduling workload, documenting quality and efficiency of the CDM group, developing and updating procedures and processes for continuous improvement, and supervision of the everyday activities of the clinical data management staff. ESSE ...[more]
Relevant Work Experience:
7+ to 10 Years
Covidien
St. Louis, MO 63042
Jul 2
Product Surveillance Specialist, Imaging A Product Surveillance Specialist, Imaging, is primarily responsible for monitoring the safety, quality and efficacy of products marketed and sold by the Covidien Imaging Solutions. Additionally, they provide technical and clinical information regarding product usage and perfomance. As a result of these activities, they will frequently develop, preserve and strengthen customer relationships which i ...[more]
