Data Reviewer Chromatographie

Description de l'entreprise **Rejoignez nos Laboratoires d’Excellence !** Avec plus de 61 000 collaborateurs dans 59 pays, Eurofins fournit des prestations d'analyses aux industries pharmaceutiques, alimentaires et dans le domaine de l'environnement. A la pointe des derniers développements en biotechnologie, en très forte croissance et leader dans son...

**Summary / purpose of the position** The Clinical Data Manager set-up and oversees the outsourced clinical data management activities for one or several assigned studies under the supervision of the Principal Clinical Data Scientist in charge of the development program. He/she is accountable (quality, budget and timelines) for the Data Management...

**Summary / purpose of the position** The Clinical Data Scientist set-up and oversees the outsourced clinical data management activities for one or several assigned studies under the supervision of the Principal Clinical Data Scientist in charge of the development program. He/she is accountable (quality, budget and timelines) for the Data Management...

Title: Clinical Data Manager H/F Company: Ipsen Innovation (SAS) Job Description: Summary / purpose of the position The Clinical Data Manager set-up and oversees the outsourced clinical data management activities for one or several assigned studies under the supervision of the Principal Clinical Data Scientist in charge of the development program....

Title: Clinical Data Manager H/F Company: Ipsen Innovation (SAS) Job Description: Summary / purpose of the position The Clinical Data Manager set-up and oversees the outsourced clinical data management activities for one or several assigned studies under the supervision of the Principal Clinical Data Scientist in charge of the development program. ...

Job OverviewWe are seeking a skilled Clinical Data Manager to join our Ipsen Pharma team. As a key member of our clinical data management team, you will play a critical role in ensuring the high-quality collection, processing, and reporting of clinical data.About the RoleThe successful candidate will have a minimum of 2 years' experience as a Clinical Data...

Short Description- Responsible for their speciality in the major maintenance and operational activities on site. This includes engineering, facilities, compliance, and implementation roles. - Job Summary- The primary focus of the Site Operations Manager is to help manage the day-to-day operations of a live data centre facility. You will be part of an...

**Summary / purpose of the position** The Clinical Data Management (CDM) Study Lead defines, implements and monitors the Data Management strategy for one or more clinical studies in Ipsen portfolio. He/She is responsible for delivering of high-quality databases by external vendors in adherence to Ipsen standards, meeting project timelines and budget. This...

About Ipsen PharmaIpsen Pharma is a leading pharmaceutical company that specializes in developing innovative treatments for rare diseases.Job DescriptionWe are seeking a highly skilled Lead Biostatistician for Clinical Data Analysis to join our team. The successful candidate will be responsible for analyzing and interpreting clinical trial data, ensuring the...

**Responsibilities**: - Review, analyze, and interpret emerging clinical trial data (including biomarkers, clinical pharmacology, and safety data) and lead preparation for key study meetings (e.g. investigator meetings, monitoring committees, advisory boards) - Partner with the study lead on oversight of clinical trial activities, including safety reviews...

QUELLES MISSIONS VOUS SERONT CONFIEES ?- Participer à l’élaboration de l'état des lieux du processus PQR actuel- Aider à l’identification des axes d'amélioration pour simplifier le processus- Automatiser les processus de collecte quand possible- Définir un mode de fonctionnement qui permette de construire les PQR de manière évolutive QUEL PROFIL...

**Summary / purpose of the position** Providing leadership and management within Neuroscience Therapeutic Area Clinical Development to provide scientific and clinical development support for products (assets) within assigned therapy area. Support development and execution of medical & clinical strategy for assigned Ipsen assets(s). Conduct scientific...

**Main responsabilities** Ensure clinical activities coordination & oversight: - Ensure efficient and thorough study start-up by overseeing the Clinical team of the CROs and working closely with other relevant team members involved in the study set up (DM, Reg, CMC etc ): to verify timely collection of essential study documents, such as regulatory and...

Please send your CV in English ! **Purpose of the position** - Take responsibility for coordinating the clinical monitoring activities, overseeing the CRO clinical /site management activities and co-monitoring the assigned international Ph2/3 clinical studies in accordance with regulatory requirements, Good Clinical Practice (GCP) guidelines and SOPs to the...

**Purpose of the position** - Take responsibility for coordinating the clinical monitoring activities, overseeing the CRO clinical /site management activities and co-monitoring the assigned international Ph2/3 clinical studies in accordance with regulatory requirements, Good Clinical Practice (GCP) guidelines and SOPs to the most rigorous standards of...

Title: Clinical Data Management Study Lead F/M Company: Ipsen Innovation (SAS) Job Description: Summary / purpose of the position The Clinical Data Management (CDM) Study Lead defines, implements and monitors the Data Management strategy for one or more clinical studies in Ipsen portfolio. He/She is responsible for delivering of high-quality databases...

**Principal Statistical Programmer** **Summary / purpose of the position** Position will participate in production/QC programming, project coordination, CRO management and oversight of vendor programming across Ipsen rare disease studies. **Main responsibilities / job expectations** **Responsibilities will include, but are not limited to the...

**Principal Statistical Programmer** **Summary / purpose of the position** Position will participate in production/QC programming, project coordination, CRO management and oversight of vendor programming across Ipsen rare disease studies. **Main responsibilities / job expectations** **Responsibilities will include, but are not limited to the...

#IpsenTraineeSquad_ **Purpose of the mission** **eTMFs Quality control**: - Perform quality control of Sponsor documents submitted to the eTMF using the established acceptable criteria. - Complete the QC workflow in either approving document or raising a quality issue to the document owner. - Ensure documents which fail TMF quality control and/or TMF...

Title: Principal Statistical Programmer H/F Company: Ipsen Innovation (SAS) Job Description: Principal Statistical Programmer Summary / purpose of the position Position will participate in production/QC programming, project coordination, CRO management and oversight of vendor programming across Ipsen rare disease studies. Main responsibilities / job...