Clinical Trial Administrator

Job Title: Clinical Trial Administrator - eTMF SpecialistCompany: IQVIAIQVIA is seeking an eTMF Specialist to join our team. The successful candidate will be responsible for reviewing eTMF plans, uploading documents, and performing quality control.Responsibilities:Review eTMF plans and ensure compliance.Upload documents to the eTMF and perform ongoing...

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...

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,...

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,...

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...

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

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

Job Summary:We are seeking an experienced Clinical Trial Supply Specialist to join our team at IQVIA. The successful candidate will be responsible for reviewing eTMF plans, uploading documents, and performing quality control of the eTMF.Key Responsibilities:Review eTMF plans and ensure compliance with regulatory requirementsUpload documents to the eTMF and...

At Iqvia, we are seeking an e-TMF Specialist - Supply section to join our dynamic team. The successful candidate will be responsible for reviewing eTMF plans, uploading documents, and performing quality control of the eTMF using Company System.Key Responsibilities:Review eTMF plans and ensure compliance with regulatory requirementsUpload documents in the...

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...

**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...

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 providing  senior 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...

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...

Job DescriptionWe are seeking an experienced Statistical Programming Leadership and Innovation Manager to join our Clinical Data Management Unit at Chiesi Group.The successful candidate will provide technical leadership and ensure high-quality statistical programming in supporting different phases of clinical development, in compliance with standards and...

Who we are looking forPurposeTo develop programs and statistical output for the management and reporting of clinical trial data managed by Global Clinical Department.To guarantee quality of statistical output produced by external provider, to program tools to support data review activities and data visualization, to collaborate on the interpretation and...

On behalf of our Client a global pharmaceutical company, IQVIA is looking for a CTS Packaging Packer, based in Parma or surrounding areas. RESPONSIBILITIES: - Packaging and labelling of non-clinical studies and stability clinical trial material - Contributes to the evaluation for the definition of packaging specifications of materials for clinic,...

On behalf of our Client a global pharmaceutical company, IQVIA is looking for a eTMF and Data Archiving who can join an exciting working environment in a dynamic atmosphere. JOB DESCRIPTION: - To ensure data management and statistics trial documentation is managed according to internal standards and regulatory requirements - To oversee activities to ensure...

Who we are looking for Purpose To develop programs and statistical output for the management and reporting of clinical trial data managed by Global Clinical Department.  To guarantee quality of statistical output produced by external provider, to program tools to support data review activities and data visualization, to collaborate on the...

Select how often (in days) to receive an alert:Statistical Programmer, Data Analyst - TemporaryDate: 13 Sep 2024Department: Global Clinical DevelopmentTeam: RD, Pharmacovigilance Regulatory AffairsJob Type: Direct EmployeeContract Type: TemporaryLocation: Parma, ITAbout usBased in Parma, Italy, Chiesi is an international research-focused pharmaceutical and...