Clinical Biomarker Principal Scientist F/m

**Title**: Scientist Clinical Biomarkers H/F **Company**: Ipsen Innovation (SAS) The clinical Biomarkers scientist will be responsible for successfully driving biomarkers activities, for multiple programs covering all three therapeutic areas (Oncology, Neuroscience, Rare Diseases), where needed. He/She will contribute to define biomarker plans for each...

**Primary responsibilities**: - Contributes to the development of clinical biomarker strategies and establishes biomarker plans for target engagement, pharmacodynamics, mechanism of action, and patient selection that are suitable for informed decision-making - Monitors clinical implementation and validation of biomarkers - Selects the most relevant...

**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...

**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...

**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...

**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...

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...

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. ...

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...

**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...

The Senior Clinical Monitoring lead is fully accountable for all clinical monitoring activities, overseeing the CRO clinical /site management activities and co-monitoring the assigned international Phase I to III clinical studies in accordance with GCP guidelines and regulations. - He/she builds strong relationships with investigators and proactively acts as...

**Purpose of the position** - Assists and provides support to the members of the clinical operations study team in administrative activities in order to facilitate the overall management of Company sponsored studies - Executes tasks as assigned by the CPM related to the conduct of clinical studies, study budget forecasting and tracking - Responsible for...

Please send your CV in English ! **Purpose of the position** - Assists and provides support to the members of the clinical operations study team in administrative activities in order to facilitate the overall management of Company sponsored studies - Executes tasks as assigned by the CPM related to the conduct of clinical studies, study budget forecasting...

Clinical Data Management Study Lead F/M Ipsen Innovation (SAS) The Clinical Data Management (CDM) Study Lead defines, implements and monitors the Data Management strategy for one or more clinical studies in Ipsen portfolio. This includes monitoring the quality, anticipating and mitigating the risks as part of the risk management plan and measuring 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...

**Purpose of the position** - Assists and provides support to the members of the clinical operations study team in administrative activities in order to facilitate the overall management of Company sponsored studies - Executes tasks as assigned by the CPM related to the conduct of clinical studies, study budget forecasting and tracking - Responsible for...

**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...

**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...

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...