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Job matches 290

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6 Month Contract - MES Specialist – Dublin – TOP 3 Pharma

Company: i-Pharm Consulting
Location: Dublin
Salary: Negotiable
Closing Date: 10 Mar 17More Details
Contract MES Specialist – Dublin – TOP 3 Pharma MES Specialist required for a top 3 leading Pharmaceutical Organisation. Contract opportunity to support the Manufacturing Execution System (MES) in use on site. To develop, update, test and verify electronic master batch records. To provide MES end user coaching, troubleshooting and support. Candidates must be eligible to work in the UK & Ireland. ...

Process Engineer - South East Ireland

Company: i-Pharm Consulting
Location: Carlow
Salary: Negotiable
Closing Date: 10 Mar 17More Details
PROCESS ENGINEER / GLOBAL PHARMA / South East A process Engineer is required for a Global Pharmaceutical company on a state of the art manufacturing site in the South East of Ireland. The successful candidate will lead multifunctional teams to complete improvement projects for IPT and actively participate and lead on-site Kaizen activates and investigations. ...

Product Quality Manager

Company: i-Pharm Consulting
Location: Berlin
Salary: Negotiable
Closing Date: 10 Mar 17More Details
Product Quality Manager (m/w)Office-based in Berlin Vollzeit- unbefristetAufgaben:- Erstellung von Strategien zur Qualitätssicherung- Entwicklung des internen QM- Systems mit den zugehörigen Fachbereichen- Koordination von Entwicklungsprojekten- Durchführung von Qualitätsmaßnahmen - Führen von Prozessoptimierungsschulungen- Unterstützung der fachübergreifenden Abteilungen in allen Belangen bezüglich QA/RAVoraussetzungen:- 3-5 Jahre Berufserfahrung in Regulatory Affairs - Abgeschlossenes tech ...

Senior Quality Manager Medizintechnik

Company: i-Pharm Consulting
Location: Berlin
Salary: Negotiable
Closing Date: 10 Mar 17More Details
Senior Quality Manager (m/w)Office-based in Berlin Vollzeit- unbefristet Aufgaben: * Sicherstellung der Qualitätsanforderungen interner Produktions- und Prüfprozesse * Entwicklung des internen QM- Systems mit den zugehörigen Fachbereichen * Durchführung interner und externern Audits * Führen von Prozessoptimierungsschulungen * Unterstützung der übergeordneten Position in QA/RA Themen Voraussetzungen: * 3-5 Jahre Berufserfahrung in Regulatory Affairs * Abgeschlossenes technisches Stu ...

(S)CRA, Sponsor-based, ganz Deutschland

Company: i-Pharm Consulting
Location: Germany
Salary: Negotiable
Closing Date: 10 Mar 17More Details
Zu Ihren Aufgaben zählen: • Durchführung von Monitoring und Close-out Visits bei den Zentren vor Ort• Verantwortlich für Site-Selection und Site-Initiation Visits je nach Studie• Bearbeitung, Kontrolle und gegebenenfalls Korrektur von studienrelevanten Dokumenten• Enge Zusammenarbeit mit den Projekt Managern, den Ärzten und Study Coordinatoren• Ansprechpartner für Ethikkommissionen und Gesundheitsbehörden• Teilnahme an Meetings und Konferenzen • Einarbeitung neuer CRAs – je nach Erfahrung • ...

Regulatory Affairs Manager (m/w)

Company: i-Pharm Consulting
Location: München
Salary: Negotiable
Closing Date: 10 Mar 17More Details
Regulatory Affairs Manager (m/w)Office-based in München Vollzeit- unbefristet Aufgaben: * Planung des nationalen und internationalen Zulassungsprozesses von Software-Medizinprodukten * Durchführung der Einreichung vorbereiteter Dokumente * nachträgliche Betreuung der eingereichten Dokumente * Schnittstelle und Ansprechpartner des Software- Entwicklungsteams zu regulatorischen Themen * Technische Dossier- Zusammenstellung nach STED Voraussetzungen: * 3-5 Jahre Berufserfahrung in Regul ...

Site Resource Manager/CRA Manager – Home Based – South West

Company: i-Pharm Consulting
Location: South West England
Salary: Negotiable
Closing Date: 10 Mar 17More Details
JOB SUMMARYThis international CRO is seeking a Lead CRA/CRA Manager to join their team and work as a Site Resource Manager. This position is home based in the South West with regional travel to sites required. This is an excellent opportunity for a Lead CRA to line manager a team of 12-14 CRA’s as well as acting as the relationship manager on site. The role requires an individual to understand the CRA role and have previous line management experience. ...

Senior CRA (m/w) – Homebased

Company: i-Pharm Consulting
Location: Germany
Salary: Negotiable
Closing Date: 10 Mar 17More Details
Senior CRA (m/w) – HomebasedEine internationale CRO sucht ab sofort eine/n Senior Clinial Research Associate (m/w) mit Erfahrung in Onkologie. Es handelt sich um eine Position in Festanstellung in einem internationalen Betriebsklima mit vielfältigen AufstiegsmöglichkeitenIHRE AUFGABEN- Selbstständige Vorbereitung, Durchführung und Überwachung der klinischen Studien gemäß der ICH/GCP - Erstellung der relevanten Studiendokumente, wie z.B. Studienprotokoll, CRF, Patienteninformation etc. ...

CRA II (m/w) München oder Home-based

Company: i-Pharm Consulting
Location: Germany
Salary: Negotiable
Closing Date: 10 Mar 17More Details
CRA II (m/w) München oder Home-basedEine internationale CRO sucht ab sofort eine/n CRA II (m/w) für den Raum München. ...

SCRA Sponsor dedicated

Company: i-Pharm Consulting
Location: Germany
Salary: Negotiable
Closing Date: 10 Mar 17More Details
SCRA (m/w) home-based, direkt beim SponsorEine gut aufgestellte und profilierte CRO bietet ein in der Branche besonderes Arbeitsklima für SCRA, die gerne regional reisen möchten. Anspruchsvolle Projekte und ein gutes Betriebsklima in Verbindung mit offenen Kommunikationsstrukturen schaffen eine solide Grundlage für Ihre langfristige berufliche Entwicklung. ...

Freelance RA Consultant (m/w) Medizintechnik IVD

Company: i-Pharm Consulting
Location: Germany
Salary: Negotiable
Closing Date: 10 Mar 17More Details
RA Consultant (m/w) Medizintechnik IVDFreiberufler/FreelancerHome-based in DeutschlandAufgaben:• Aktive Mitarbeit bei den Zulassungsverfahren für Europa• Überarbeitung der Technischen Dokumentation• Bearbeitung der CE Konformitätsbewertungsverfahren• Mitarbeit im Risikomanagment nach EN ISO 14971• Direkter Ansprechpartner für benannte Stellen• Entwicklungsbegleitende RA Beratung in Hinsicht auf internationale ProduktersteinführungIhr Profil: • Technisches Studium der Ingenieur- oder naturwis ...

Associate Director of Regulatory Affairs

Company: i-Pharm Consulting
Location: England
Salary: Negotiable
Closing Date: 10 Mar 17More Details
Associate Director of Regulatory Affairs Are you an experienced Regulatory professional looking to move into an Associate Director role? Do you have extensive clinical development, strategy and line management experience? Are you a Manager/Senior Manager looking for more responsibility? Are you looking to work for a very well respected Top 10 CRO? Are you passionate about Regulatory Affairs? Then this is the role for you. ...

Business Development Manager (m/w)

Company: i-Pharm Consulting
Location: Leipzig
Salary: Negotiable
Closing Date: 10 Mar 17More Details
Business Development Manager (m/w)Office-based in LeipzigFür ein mittelständisches und schnell wachsendes CMO suchen wir einen Business Development Manager. Falls Sie Erfahrung im Business Development sammeln konnten und nach einer neuen Herausforderung suchen, dann bewerben Sie sich. ...

Chemist in Analytical Development (m/f)

Company: i-Pharm Consulting
Location: München
Salary: Negotiable
Closing Date: 10 Mar 17More Details
Chemist in Analytical Development (m/f)Office-based in MunichRole / Description:? As analytical chemist in the Laboratory, your main responsibilities are around performing analytical testings and analytical method development? Main methods used are HPLC and GC, as well as LC-MS and GC-MS? Moreover you will work on proper laboratory documentation? Report writing and analysis of results is also within your expertiseRequirements:? Degree in chemistry, or equivalent vocational training as a chem ...

Director of Regulatory Affairs

Company: i-Pharm Consulting
Location: Surrey
Salary: Negotiable
Closing Date: 10 Mar 17More Details
Director of Regulatory AffairsAre you an experienced Regulatory professional looking to move into a Director role? Do you have extensive clinical development, strategy and line management experience? Are you looking to work for a very well respected Top 10 CRO? Are you passionate about Regulatory Affairs?Job Title: Regulatory Affairs DirectorLocation: Office based from anywhere in EuropeBenefits: Above market rate salary + benefitsJob Responsibilities:• Responsibility for the management and ...

SCRA - Neurologia + kilku sponsorow - Mazowieckie

Company: i-Pharm Consulting
Location: Masovia
Salary: Negotiable
Closing Date: 10 Mar 17More Details
SCRA - Neurologia + kilku sponsorow - MazowieckieI am looking to speak to experienced SCRA's in Poland with minimum of 4 years experience. You will be a confident monitor open to take on new challenges of leading projects alongside local study leader. We are looking for strong experience as a SCRA as well as some experience as a Lead CRA. ...

Clinical Research Associate (CRA) – UK-wide; flexible location

Company: i-Pharm Consulting
Location: England
Salary: Negotiable
Closing Date: 10 Mar 17More Details
My client, a privately owned global CRO who is an active player in drug and medical device research. They have strong strategic partners within a select group of leading sponsors, aiming to offer the most efficient and cost-effective path to product approval. Moreover, my client is offering the opportunity to work with market leading therapeutic, regulatory and operational experts whose combined experience ensures the advancement of medical devices and pharmaceutical agents. ...

Senior CRA/ CRA – South of England – Home office

Company: i-Pharm Consulting
Location: South West England
Salary: Negotiable
Closing Date: 10 Mar 17More Details
My client, a global CRO with extensive operations throughout the UK, is currently recruiting Senior CRAs and CRAs with predominantly regionalised travel in the South of England. The ideal candidate will have one years’ monitoring experience on a number of studies throughout the UK.BENEFITS• Excellent career progression, training and support.• Exposure to a diverse range of studies including MS, Cardiovascular and Oncology. ...

CRA/ Senior CRA – Oncology – UK Wide

Company: i-Pharm Consulting
Location: England
Salary: Negotiable
Closing Date: 10 Mar 17More Details
Of recent, we have seen an increased demand for experienced CRAs with strong oncology monitoring experience. My client, a top-5 CRO, is currently expanding their team in the UK as a result of a new relationship recently established with a major US pharmaceutical organisation. This is an excellent opportunity for a candidate looking for reduced monitoring, the opportunity to work on oncology studies, as well as a healthy work-life balance. ...

Biostatistiker (m/f) PK/PD Modellierung

Company: i-Pharm Consulting
Location: München
Salary: Negotiable
Closing Date: 10 Mar 17More Details
Biostatistiker (m/f) PK/PD ModellierungOffice-based in MünchenAufgaben:• Als Biostatistiker (m/f) PK/PD Modellierung sind Sie in einem Team verantwortlich für alle Aktivitäten rund um das Thema statistische Modellierung und Simulation• Im Umfeld klinische Studien stellen Sie Ihre Expertise zur Verfügung in Bezug auf die Optimierung von Studiendesigns, der Erstellung von statistische Modellierungsplänen sowie das Verfassen von Berichten zur Entscheidungsfindung bei internen Beschlüssen• Absch ...

Drug Safety Specialist (URGENT - 12 Months - Thames Valley)

Company: i-Pharm Consulting
Location: Berkshire
Salary: Negotiable
Closing Date: 09 Mar 17More Details
DRUG SAFETY SPECIALIST (PHARMACEUTICAL - 12 MONTHS - THAMES VALLEY)JOB OVERVIEW:- We are recruiting for a Drug Safety Specialist on a 12-month contract initially (possibility of an extension) for a large Pharmaceutical situated in the Thames Valley- Start date mid-March 2017 and an excellent daily rate (to be discussed)RESPONSIBILITIES:- Support the Director of Drug Safety in the tracking of CAPA’s, planning and deviations resulting from inspections, internal audits and inspections- Supervis ...

Stredne velké CRO,30 zamestnancu hledá CRA II/ CRA III

Company: i-Pharm Consulting
Location: Czech Republic
Salary: Negotiable
Closing Date: 09 Mar 17More Details
Významné globální CRO hledá v rámci rozšírení týmu odborníku v klinickém hodnocení léciv pro své aktivity novou kolegyni/ kolegu na pozici CRA. Náš klient má velmi stabilní postavení na Ceském trhu již mnoho let. Skvelá možnost kariérího rustu a zamenaneckých benefitu. ...

Junior Contract Lawyer - Pharmaceutical industry - BE

Company: i-Pharm Consulting
Location: Zaventem
Salary: Negotiable
Closing Date: 09 Mar 17More Details
*BRAND NEW* Junior Contract Lawyer - Pharmaceutical industry - BE*Over mijn cliënt*Marktleider in het domein van klinische ondezoek Aanwezig in meer dan 45 landen met meer dan 85 kantoren wereldwijdZijn succes is te danken aan het gebruik van innoverende technologieën en therapeutische expertise *Over de functie*- contract onderhandelingen (opstellen, herzien, onderhandelen en finaliseren) met de study site en dit in overeenstemming met interne en externe regels- budget onderhandeling- je wa ...

Monitor Badan Klinicznych - Praca zdalna - Samochod sluzbowY

Company: i-Pharm Consulting
Location: Warsaw
Salary: Negotiable
Closing Date: 09 Mar 17More Details
Monitor Badan Klinicznych - Praca zdalna - Samochod sluzbowy Our client is a Global CRO that is gradually expanding its monitoring team in Poland due to the strength and stability of the clinical operations market. Growing company offers great future opportunities for further career growth and development; all employees work together in reaching mutual company goals whilst developing professionally thanks to the tools provided. ...

Site Contract Specialist (m/w) Office-Based, DE German Speaking

Company: i-Pharm Consulting
Location: Germany
Salary: Negotiable
Closing Date: 09 Mar 17More Details
For our client, an international company we are looking for an experienced Site Contract Specialist to be a part of the regulatory start up department. With good interpersonal skills and fluent German language skills, you are perfectly placed to join the team. ...

CRA II & SCRA - Oncology focus / Denmark

Company: i-Pharm Consulting
Location: Copenhagen
Salary: Negotiable
Closing Date: 09 Mar 17More Details
If you are interested to work from home, with location anywhere in Denmark; as well as keen to be part of the stable International organisation - get in touch now. This is an Oncology focus CRA role, so strong background within this TA is a must. I am currently representing Global CRO which is offering an exciting home based opportunity. ...

CRA (m/w), office-based, München

Company: i-Pharm Consulting
Location: München
Salary: Negotiable
Closing Date: 09 Mar 17More Details
Für eine mittelständische CRO suche ich aktuell einen CRA (m/w) mit erster Berufserfahrung für eine Anstellung direkt beim Sponsor. ...

CTA & SrCTA /// Espoo, Helsinki // Pharma company

Company: i-Pharm Consulting
Location: Espoo
Salary: Negotiable
Closing Date: 09 Mar 17More Details
Fantastic opportunity for a current CTA/SrCTA located within Greater Helsinki area. Company is offering a stable long term growth within an organisation and ability to be part of a Global structure with massive projects. SUMMARY CTA / Clinical Trial Administrator required for permanent position with Pharmaceutical Company based near Helsinki/Espoo. ...

Quality Head (m/f)

Company: i-Pharm Consulting
Location: Basel
Salary: Negotiable
Closing Date: 09 Mar 17More Details
Quality Head (m/f) Office-based in BaselMy client, an international pharmaceutical company, is looking for a Quality Head for their site in Basel. You will lead the QA Team as well as establish and improve the existing Quality System. You will be the responsible person for all quality matters, for the company's own production as well as the custom manufacturing arm of the plant. ...

BTA / Biologisch Technischer Assistent (m/w)

Company: i-Pharm Consulting
Location: Hamburg
Salary: Negotiable
Closing Date: 09 Mar 17More Details
BTA / Biologisch Technischer Assistent (m/w)Office-based in HamburgAufgaben:? Analytiche Untersuchung von Pharmazeutika und und Biotechnologischen Arzneiformen gemäß gültiger Richtlinien? Dokumentation der Ergebnisse und enge Zusammenarbeit mit der Qualitätssicherungsabteilung? Arbeit nach GMP und ISO Normen ? Sicherstellung einer selbständigen, schnellen und ordentlichen Bearbeitung der ProbenVoraussetzungen:? Abgeschlossene Berufsausbildung als Biologisch-technischer Assistent, Biologielab ...
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