About us Chiesi is an international research-focused biopharmaceutical group with 90 years’ experience, operating in more than 30 countries, with its Headquarter in Parma, Italy. More than 8,000 employees across the group are united by a
Chiesi Corporate Functions Global Human Resources The HR Team welcomes and guides people through every step of their journey, supporting the creation of space for personal fulfillment and professional growth. The Global HR Department promotes internal growth through
About us Chiesi is an international research-focused biopharmaceutical group with 90 years’ experience, operating in more than 30 countries, with its Headquarter in Parma, Italy. More than 8,000 employees across the group are united by a
Chiesi Research & Development Our R&D team represents a fundamental asset for the business. It is divided into integrated functional areas focusing on pipeline projects including discovery and preclinical research, global technical development, drug delivery technology, clinical
About us Chiesi is an international research-focused biopharmaceutical group with 90 years’ experience, operating in more than 30 countries, with its Headquarter in Parma, Italy. More than 8,000 employees across the group are united by a
About us Chiesi is an international research-focused biopharmaceutical group with 90 years’ experience, operating in more than 30 countries, with its Headquarter in Parma, Italy. More than 8,000 employees across the group are united by a
Principal Regulatory Writer, Global Rare Diseases Department: GRD Regulatory Affairs Business Area: R&D, Pharmacovigilance & Regulatory Affairs Job Type: Direct Employee Contract Type: Permanent Location: Parma, IT What we are looking for This is what you will
Chiesi Farmaceutici S.p.A. in Parma is seeking an experienced Clinical Operations Lead to provide strategic and operational leadership for clinical development programs. This role involves ensuring integration of Clinical Operations activities across multiple phases and acting
Chiesi Farmaceutici S.p.A. is seeking a Clinical Research Physician in Parma, Italy, to support global clinical studies in rare diseases. The role includes responsibilities like conducting medical reviews, interfacing with external experts, and ensuring the scientific validity of
Experteer OverviewIn this role, you lead the global publication strategy and execution for studies with worldwide impact, aligning scientific outputs with medical and commercial objectives. You’ll orchestrate integrated publication plans, manage congress and journal activities, and oversee manuscript
Experteer Italy is seeking a professional to lead the global publication strategy and execution for impactful studies. This role requires an advanced degree, ideally an MD or PhD, along with 2+ years of relevant experience in pharmaceutical companies.The
Experteer Overview In this role you will author, review, and manage regulatory documents that translate clinical, nonclinical, and CMC data into compliant submissions for global authorities. You will serve on cross‑functional teams to ensure scientific rigor and
Principal Regulatory Writer, Global Rare Diseases Department: GRD Regulatory Affairs Business Area: R&D, Pharmacovigilance & Regulatory Affairs Job Type: Direct Employee Contract Type: Permanent Location: Parma, IT What we are looking for This is what you will
Clinical Research Physician, Global Rare Diseases Department: GRD Clinical Development Business Area: R&D, Pharmacovigilance & Regulatory Affairs Job Type: Direct Employee Contract Type: Permanent Location: Europe (flexible) – remote or hybrid What you will do Support the
Chiesi is an international research-focused biopharmaceutical group with 90 years’ experience, operating in more than 30 countries, with its Headquarter in Parma, Italy. More than 8,000 employees across the group are united by a singular purpose:
Business Area: R&D, Pharmacovigilance & Regulatory Affairs Job Type: Direct Employee Contract Type: Temporary Location: Parma, IT About us Chiesi is an international research-focused biopharmaceutical group with 90 years’ experience, operating in more than 30 countries,
Experteer OverviewIn this Senior Process Scientist role, you will lead process development and manufacturing oversight for gene therapy programs within Chiesi Global Rare Diseases, focusing on synthetic nucleotides and RNA-guided editing components. You will serve as SME
Who we are looking for This is what you will do End to end execution of assigned innovation and initiatives, translating strategies and study designs on time, quality, and compliant delivery across programs, therapeutic areas and geographies
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This is what you will do An experienced Clinical Operations Lead with a strong background in global drug development, capable of providing strategic and operational leadership across complex clinical development programs. The Clinical Operations Lead (COL) ensures