Clinical Data Management Unit Manager

**Date**:12 Nov 2024**Department**:Global Clinical Development**Team**:R&D, Pharmacovigilance & Regulatory Affairs**Job Type**:Direct Employee**Contract Type**:Permanent**Location**:Parma, IT**Purpose** - To provide technical leadership and ensure high quality statistical programming in supporting different phases of clinical development in compliance with...

Team: R&D, Pharmacovigilance & Regulatory AffairsJob Type: Direct EmployeeContract Type: PermanentLocation: Parma, ITPurposeTo provide technical leadership and ensure high quality statistical programming in supporting different phases of clinical development in compliance with standards and regulatory requirements.To lead the team providing senior expertise...

PurposeTo provide technical leadership and ensure high quality statistical programming in supporting different phases of clinical development in compliance with standards and regulatory requirementsTo lead the team providingsenior expertise and guidance, planning resources, recruiting, mentoring and developing the team To foster the power of data...

Team: R&D, Pharmacovigilance & Regulatory AffairsJob Type: Direct EmployeeContract Type: PermanentLocation: Parma, ITPurposeTo provide technical leadership and ensure high quality statistical programming in supporting different phases of clinical development in compliance with standards and regulatory requirements.To lead the team providing senior expertise...

Team: R&D, Pharmacovigilance & Regulatory Affairs Job Type: Direct Employee Contract Type: Permanent Location: Parma, IT Purpose To provide technical leadership and ensure high quality statistical programming in supporting different phases of clinical development in compliance with standards and regulatory requirements. To lead the team providing...

Team: R&D, Pharmacovigilance & Regulatory Affairs Job Type: Direct Employee Contract Type: Permanent Location: Parma, IT Purpose To provide technical leadership and ensure high quality statistical programming in supporting different phases of clinical development in compliance with standards and regulatory requirements. To lead the team providing senior...

Purpose To provide technical leadership and ensure high quality statistical programming in supporting different phases of clinical development in compliance with standards and regulatory requirements To lead the team providing  senior expertise and guidance, planning resources, recruiting, mentoring and developing the team  To foster the power of...

Team: R&D, Pharmacovigilance & Regulatory AffairsJob Type: Direct EmployeeContract Type: PermanentLocation: Parma, ITPurposeTo provide technical leadership and ensure high quality statistical programming in supporting different phases of clinical development in compliance with standards and regulatory requirements.To lead the team providing senior expertise...

Job OverviewWe are seeking an experienced Data Management Team Lead to join our Clinical Trials team at Chiesi Group.Key ResponsibilitiesTo provide technical leadership and ensure high-quality statistical programming in supporting different phases of clinical development, in compliance with standards and regulatory requirements.To lead the team providing...

About the RoleWe are seeking a Data Management Leader to provide technical leadership and ensure high-quality statistical programming in supporting different phases of clinical development. As part of our R&D, Pharmacovigilance & Regulatory Affairs team, you will be responsible for leading a team, providing senior expertise and guidance, planning resources,...

What you'll be doing day to day • Lead and manage the execution of Ingka Facility Management (FM) within the unit(s) through the unit FM team • Responsible to make sure that each property is managed throughout its lifetime including safety, compliance, maintenance and improvement to ensure a safe and operational environment for the business, colleagues,...

What you'll be doing day to day • Lead and manage the execution of Ingka Facility Management (FM) within the unit(s) through the unit FM team• Responsible to make sure that each property is managed throughout its lifetime including safety, compliance, maintenance and improvement to ensure a safe and operational environment for the business, colleagues,...

Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it's the best of both worlds. ClinChoice, is searching for an experienced Senior Project Manager/Director to work with one of our pharmaceutical partners, to oversee Clinical Project...

**Job ID**: 256102 **Date posted**: 02/09/2024 PURPOSE OF JOB We take the lead in delivering safe, compliant, sustainable and innovative property solutions - with Democratic design and life cycle cost on top of our mind. We actively maintain and secure that our properties are kept in relevant shape for the business. WHAT YOU'LL NEED TO HAVE - Preferred...

**Date**:4 Nov 2024**Department**:Global Pharmacovigilance**Team**:R&D, Pharmacovigilance & Regulatory Affairs**Job Type**:Direct Employee**Contract Type**:Permanent**Location**:Parma, IT**_About us_** - Based in Parma, Italy, Chiesi is an international research-focused pharmaceutical and healthcare group with over 85 years’ experience, operating in 31...

On behalf of our Client a global pharmaceutical company, IQVIA is looking for **a e-TMF Specialist - Supply section** who can join an exciting working environment in a dynamic atmosphere. **RESPONSIBILITIES**: - To review eTMF plans - To upload documents in the eTMF and perform ongoing quality control of the eTMF (Investigational products and Clinical...

About UsChiesi, a leading pharmaceutical and healthcare company, is based in Parma, Italy. With over 85 years of experience and operations in 31 countries, the company has a strong presence globally.We are committed to improving people's quality of life by acting responsibly towards society and the environment. Our mission drives us to research, develop, and...

Who we are looking forPurposeTo support and facilitate the clinical risk assessment and management activities in GCD clinical studies in compliance with regulations and guidelines (including escalation and specific reporting).Main ResponsibilitiesCollaborates with GCD (Global Clinical Development Dept) clinical study teams for:•    Quality-by-design...

Who we are looking for Purpose The “Global Pharmacovigilance Operations Unit Head, Care” supports the Global Pharmacovigilance Team (within R&D) in the execution and oversight of premarket and postmarket pharmacovigilance operations activities within the “Care” Business Unit. Main Responsibilities •    Collaborate...

Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it's the best of both worlds. ClinChoice is searching for a Clinical Trial Assistant (CTA) to join an international pharmaceutical company, with a focus on Respiratory, Paediatrics,...