(posté le 23/062008)

Non-clinical Drug Safety Scientist SERVIER

You will be in charge of the management on non-clinical Safety Pharmacology programmes to support the development and regulatory submissions of new drug discovery candidates. Located in our London office, you will implement the regulatory studies in close partnership with leading international CROs with an overall responsibility for the scientific, technical and regulatory study conduct.

The successful applicant will have BSc, MSc, a proven practical and scientific experience together with organisational abilities. Up-to-date knowledge in current regulatory requirements of new drug development in a GLP compliant environment, as well as some experience within a research or industrial environment would be an advantage.

A background in physiology of central nervous system or cardiovascular function would be required.

You are self-motivated, collaborative and team oriented with good communication skills.

To apply, please send your application (cover letter and CV), quoting reference, to:

Garlone VIOLLE

SERVIER, 11 rue des Moulineaux, 92150 Suresnes FRANCE

e-Mail : valerie.pesenti@fr.netgrs.com

(posté le 07/052008)

Médecin délégué Centre de Recherche Clinique Amiens

Le Centre de Recherche Clinique (CRC) du CHU d'Zmiens recherche un médecin délégué afin d'assurer le suivi médical des études du CRC en accord avec le protocole et les BPC. Docteur en médecine vous avez une expérience en recherche biomédicale. Le poste est un CDD de 3 ans." Contact Sophie LIABEUF 03-22-45-60-85 ou liabeuf.sophie@chu-amiens.fr.

(posté le 14/04/2008)

Head of CRO-Lab operations in preclinical pharmacology

 UROsphere is a preclinical contract research organization (CRO), which provides pharmacological services to the (bio)pharmaceutical industry, that combines  a high-level scientific know-how, preclinical competences, and a performing technical platform. It helps its clients to develop effective drugs for genito-urinary (GU) disorders including urinary incontinence (UI), overactive bladder (OAB), Benign Prostatic Hyperplasia (BPH), sexual dysfunctions and renal pathologies.  

 Young and with a unique position in its specialty field, UROsphere is planning its development for the forthcoming years and searches reliable personnel with high potential to work in Toulouse, France.

 Under the supervision of the Director of Operations, you will drive the overall performance of the CRO-technical platform; and will be in charge of the production of scientific results, in accordance with client’s requirements and within the frame of study protocols.

 Your job will be to deliver on-time data and reports to the Director of Operations. You will be responsible for client satisfaction on quality, delays and costs containment of the experiments.

You will conduct the scientific, technical and administrative management of the team; develop and manage laboratory budgets, technology plans and operational plans.  You will ensure that both testing and support staff is available, trained and competent to meet the workload needs of the laboratory and adequately supervise, recruit, develop and evaluate it. You will set up, develop and/or support process improvement initiatives.
You will participate with the Director of Research in the planning and management of scientific partnerships with other (private and public) labs and serve as a senior local scientific expert.

You have a Ph.D. or equivalent experience in pharmacology and/or physiology (ideally in the preclinical urology field) and a minimum 5 years of management experience in a Contract Research Organization or within Pharmaceutical Industry (Central Lab/Specialty Provider) with GLP environment constraints. You have already shown strong problem-solving skills and are fluent in French and English languages.

 If you are interested in this position, please send your resume and cover letter with your motivations to sophie.dubois@uropshere.com, or to Sophie Dubois, UROsphere

Faculté des Sciences Pharmaceutiques, 35, chemin des Maraîchers, 31062 TOULOUSE Cedex 09

(posté le 05/02/2008)

PROJECT LEADER IN NON-CLINICAL SAFETY PHARMACOLOGY Job code : SPH

You will be in charge of the management on non-clinical Safety Pharmacology programmes to support the development and regulatory submission of new drug discovery candidates. Located in our London office and reporting to the head of safety Pharmacology based near Paris, you will implement the regulatory studies in close partnership with leading international CROs . As an expert in Safety Pharmacology, you will work in a highly collaborative interdisciplinary and team-based environment. In collaboration with the other team members (Pharmacology, Chemistry, Toxicology, Pharmacokinetics…) you will be in charge of the preclinical evaluation of these compounds and the preparation of the IND application. With a PhD in Pharmacology, Toxicology or MD, DVM or Pharmacist, you have a comprehensive knowledge of cardiovascular research with an experience in cellular or molecular mechanisms mediating cardiac physiological functions or pathophysiological processes. Hands-on experience in haemodynamic and ECG evaluation in rodents as well as in non rodents cardiovascular models (primates , dogs) is required. You are experienced in non-clinical drug development or toxicology, in the context of GLP multisite studies, in preparing study reports for regulatory submissions. You are self-motivated, collaborative and team oriented with good communication skills

To apply, please send your application (cover letter and CV), quoting reference, to: Céline LARQUETOUX SERVIER, 11 rue des Moulineaux 92150 Suresnes FRANCE e-Mail : celine.larquetoux@fr.netgrs.com

(posté le 30/10/2007)

Le Centre d’Investigation Clinique du CHRU de Tours, structure mixte CHRU – INSERM (INSERM CIC-202) est à la recherche d’un médecin délégué.

Le poste est disponible dès maintenant et doit être pourvu de façon urgente. Ce poste pourrait intéresser un Pharmacologue - Clinicien, en attente d’un autre poste ou ne souhaitant pas donner une orientation définitive à sa carrière … en sachant que si un candidat est intéressé sur le plus long terme, un poste de Praticien Hospitalier plein-temps a été financé par les instances.

Pour plus de précisions concernant le profil de poste, les modalités pratiques et les conditions de recrutement, merci de contacter au plus tôt : Pr Philippe Goupille Service de Rhumatologie, Hôpital Trousseau Tel : 02 47 47 59 17 (Secrétariat) e.mail: goupille@med.univ-tours.fr

(posté le 16/10/2007)

L équipe de Chimiogénomique et Pharmacogénomique du laboratoire « Biomolécules, Biotechnologie et Innovation thérapeutique UMR CNRS 7175, dispose d un financement de thèse (allocation de recherche du Ministère, Financement de Septembre 2007).
La thématique de recherche proposée porte sur » l utilisation des cellules souches pour accélérer le processus de découverte de médicaments pour les maladies rares et le cancer ».
Les candidats sont invités à prendre contact avec :
Marie-Claude KILHOFFER Equipe de Chimiogénomique et pharmacogénomique Faculté de Pharmacie 74, Route du Rhin 67401 ILLKIRCH
Tel 03 90 24 42 65 email : kilhoffer@pharma.u-strasbg.fr

Voir le descriptif complet

(posté le 16/10/2007)

Le service de Pharmacologie de l'Hôpital Européen Georges Pompidou/INSERM UMRS872 (Equipe 1) (Pr Boutouyrie/Pr Laurent) recherche un moniteur d'essai clinique et deux investigateurs d'essai clinique dans le cadre de réalisation d'essais cliniques cardiovasculaires.

Voir les annonces: Investigateurs d'essai clinique - Moniteur d'essai clinique

(posté le 15/10/2007)

Senior Pharmacologist, Pain & Inflammation

Porsolt & Partners Pharmacology is an internationally known Contract Research Organisation offering a full range of efficacy and safety tests in preclinical in vivo pharmacology. We are now looking to expand our offer in the area of pain and would like to recruit a young scientist to help us achieve this objective.

Here is a brief description of the post and the type of person we are looking for:

The position would involve responsibility for a small group of technicians (initially 1 or 2) working on models of acute, inflammatory and neuropathic pain. The successful candidate is expected to develop our existing models as well as introduce new ones to enable us to offer a comprehensive service in this important area. A practical knowledge of these models and a good understanding of their relevance to clinical pain states are essential. The ideal candidate will show enthusiasm and initiative and have some relevant experience up to doctorate or post-doctorate level.

The post will be based at our labs near Laval.

If you are interested, please forward your resume together with a cover letter to our Scientific Director, Dr. Paul Moser. Porsolt & Partners Pharmacology 9 bis rue Henri Martin 92100 Boulogne-Billancourt, FRANCE E-mail : pmoser@porsolt.com

(posté le 15/10/2007)

XCELL EXECUTIVE SEARCH is currently searching for clinical Pharmacologists for a global Pharmaceutical business based in Basel, switzerland.

 If you are interested please contact christine.moisan@xlmanager.com or +33 (0) 1 41 31 55 00

Job descriptions: Project Clinical Pharmacologist - Senior Clinical Pharmacologist

(posté le 15/10/2007)

Head of Clinical Pharmacology/Senior Manager Clinical Pharmacology

Our client is a major player in the OTC sector and has exciting opportunities within its clinical pharmacology group in Europe.

Responsible, on a global basis, for providing expertise in clinical pharmacology (phase I development) across therapeutic areas, for clinical development projects, marke­ted products and during evaluation of new product opportunities.  He/she will ensure that studies are planned, executed and reported to meet state-of-the-art industry standards and regulatory requirements.

For further information, please contact Sue Harris on 44 (0)1344887441 or email sue.harris@andersenpiquet.com