Clinical Trial Administrator

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,...

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...

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...

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...

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...

**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...

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...

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...

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 TMF...

Date: 12 Oct 2024 Department: Global Clinical Development Team: RD, Pharmacovigilance Regulatory Affairs Job Type: Direct Employee Contract Type: Temporary 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 countries with more than...

Date: 12 Oct 2024 Department: Global Clinical Development Team: R&D, Pharmacovigilance & Regulatory Affairs Job Type: Direct Employee Contract Type: Temporary 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 countries with...

Date: 12 Oct 2024 Department: Global Clinical Development Team: R&D, Pharmacovigilance & Regulatory Affairs Job Type: Direct Employee Contract Type: Temporary 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 countries...