Clinical Contract Associate

**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...

**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...

**Title**: Global clinical project manager **Company**: Ipsen Innovation (SAS) Oversee and drive all aspects of the assigned global international clinical study(ies) (Phase I to III) outsourced to a CRO in respect of planning/timelines, quality, budget and defined goals Drive execution and report activities in conjunction with Clinical Development Program...

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...

The clinical Biomarkers principal scientist will be responsible for defining the biomarker strategy, from biomarker identification, through clinical implementation, and up to companion diagnostics development, for multiple programs covering all three therapeutic areas, where needed. He/She will also be responsible for monitoring biomarkers in clinical...

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...

**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...

**Title**: Solicited Programs Associate - 6 months **Company**: Ipsen Innovation (SAS) Within the Global Patient Safety (GPS) organization, the Solicited Programs Associate will ensure full compliance with efficient processes for safety-related aspects of all solicited programs conducted at Ipsen which comprise: interventional clinical trials,...

Start: ASAPContract Length: 6 monthstime on site: 2-3 days a week Key Responsibilities and Tasks Clinical Study QA Representative• Act as QA representative for assigned clinical studies to ensure compliance with Good Clinical Practices (GCP) and regulatory requirements.• Provide timely quality-related guidance to study teams and participate in project...

Start: ASAPContract Length: 6 monthstime on site: 2-3 days a week Key Responsibilities and Tasks Clinical Study QA Representative• Act as QA representative for assigned clinical studies to ensure compliance with Good Clinical Practices (GCP) and regulatory requirements.• Provide timely quality-related guidance to study teams and participate in project...

Start: ASAPContract Length: 6 monthstime on site: 2-3 days a week Key Responsibilities and Tasks Clinical Study QA Representative• Act as QA representative for assigned clinical studies to ensure compliance with Good Clinical Practices (GCP) and regulatory requirements.• Provide timely quality-related guidance to study teams and participate in project...

Start: ASAP Contract Length: 6 months time on site: 2-3 days a week Key Responsibilities and Tasks Clinical Study QA Representative • Act as QA representative for assigned clinical studies to ensure compliance with Good Clinical Practices (GCP) and regulatory requirements. • Provide timely quality-related guidance to study teams and participate...

Johnson & Johnson is the largest and most broadly-based healthcare company in the world. We’re producing life-changing breakthroughs every day and have been for the last 130 years. The combination of new technologies and your expertise enables amazing things to happen. Teams from J&J’s consumer business are creating digital tools to help people track...

**Purpose of the Position** Sr. Manager of Training will be responsible for developing and administering Job level training for each role within Clinical Operations. They are also responsible for developing and administering Therapeutic area training for the studies **Main Responsibilities & Technical Competencies** - Developing and executing training...

Start: ASAP Contract Length: 6 months time on site: 2-3 days a week Key Responsibilities and Tasks Clinical Study QA Representative • Act as QA representative for assigned clinical studies to ensure compliance with Good Clinical Practices (GCP) and regulatory requirements. • Provide timely quality-related guidance to study teams and participate in...

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...

**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: 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...

**#LI-Remote** LI-MC1 **Summary / purpose of the position** Position will participate in exploratory programming, project coordination, CRO management and QC of vendor programming across therapeutic areas of Oncology and Rare Disease, to ensure the efficiency and quality of Biostatistical/Programming deliverables in support of Health Technology...