Lavoro clinical trial Parma

A leading pharmaceutical company is seeking a Clinical Trial Documentation & Records Management Lead in Parma, Italy. This role involves establishing and improving the documentation unit, ensuring compliance with regulatory standards. Ideal candidates will have 8-10 years of clinical operations experience, strong leadership skills, and knowledge of eTMF and CTMS systems. Flexible hybrid working...

Select how often (in days) to receive an alert: Clinical Trial Documentation & Records Management Lead Department: Global Clinical Development Business Area: 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...

On behalf of our Client - Chiesi Farmaceutici, one of the top 50 pharmaceutical companies in the world, with more than 80 years of experience within the pharmaceutical and biotechnology industry a global pharmaceutical company - IQVIA is looking for a eTMF Specialist who can join an exciting working environment in a dynamic atmosphere. This position will oversee the global eTMF (electronic Trial...

Who we are looking for This is what you will do The Clinical Trial Documentation Records Management Lead is responsible for establishing, leading, and continuously improving the Clinical Trial Documentation Records Management Unit within Chiesi GCD. This role ensures alignment between organizational and technical requirements for clinical trial documentation and records, driving the adoption and...

Social network you want to login/join with: Senior Clinical Research Associate, parma col-narrow-left Client: Teleflex Location: Job Category: Other - EU work permit required: Yes col-narrow-right Job Reference: 8556790222002585600337114 Job Views: 2 Posted: 27.08.2025 Expiry Date: 11.10.2025 col-wide Job Description: POSITION SUMMARY: The Senior Clinical Research Associate...

Senior Clinical Research Associate (Oncology) Working embedded with a leading global oncology-focused biopharmaceutical company We are partnering with a top-tier global biopharmaceutical organisation to support a growing oncology portfolio and are seeking an experienced Clinical Research Associate to join the team in an advanced, hands-on clinical role. This position offers the opportunity to...

CPL & TAYLOR by Synergos is recruiting: CLINICAL BUSINESS PARTNER LIFE SCIENCES (Ref. ANN417222) LOCATION: Full remote CONTRACT: Permanent, full-time COMPENSATION: To be defined based on experience The Company A leading international organization specializing in consulting and digital solutions for the Life Sciences sector, headquartered in Italy. Founded in 2010, the company supports...

POSITION SUMMARY:The Senior Clinical Research Associate (Senior CRA) is responsible for scheduling and conducting on-site and remote monitoring visits in compliance with applicable regulatory standards (MDR, ISO *****, ICH/GCP guidelines, Teleflex procedures and IRB/EC policies and procedures). The Senior CRA conducts monitoring visits as identified by the monitoring plan, study team or...

Purpose To manage the administrative and documentation aspects of clinical trials at every stage of the process (study documentation, maintaining databases, creating/ updating trackers and support with supplies management) Main Responsibilities Support the CPM in preparation of study TMF Plan and Map, and other Clinical Study Plans as required Maintains paper/electronic TMF and electronic...

A global pharmaceutical company in Parma, Italy, seeks a Clinical Pharmacologist Lead with over 5 years of industry experience to oversee clinical pharmacology strategies. Responsibilities include leading Clinical Development Programs, designing trial protocols, and integrating innovative methodologies. The ideal candidate will have an MD or PhD, proven leadership in pharmacokinetics and...

A leading pharmaceutical company in Parma, Italy, seeks a Clinical Trial Documentation & Records Management Lead to ensure compliance with regulatory standards and manage clinical trial technologies. The ideal candidate has 8-10 years of experience in clinical operations and a robust understanding of eTMF and CTMS. This role emphasizes team leadership, cross-functional collaboration, and...

A leading medical device company in Parma is seeking a Senior Clinical Research Associate to conduct monitoring visits and ensure compliance with regulatory standards. The ideal candidate has over 5 years of experience in clinical trial monitoring and possesses strong organizational and communication skills. This role includes responsibilities such as evaluating data accuracy and training...

A leading pharmaceutical company in Parma, Italy, seeks a Clinical Trial Documentation & Records Management Lead to ensure compliance with regulatory standards and manage clinical trial technologies. The ideal candidate has 8-10 years of experience in clinical operations and a robust understanding of eTMF and CTMS. This role emphasizes team leadership, cross-functional collaboration, and...

Who we are looking for Purpose The Senior Clinical Research Physician provides scientific and strategic leadership in the design, execution, and interpretation of global clinical studies in the non-obstructive respiratory diseases therapeutic area. They will drive the preparation of documents for regulatory submissions, ensuring the scientific validity and rigor of key documents, including...

Join to apply for the Clinical Pharmacologist Lead role at Chiesi Group Based in Parma, Italy, Chiesi is an international research-focused pharmaceutical and healthcare group with 90 years’ experience, operating in 31 countries with more than 7,000 employees (Chiesi Group). To achieve its mission of improving people’s quality of life by acting responsibly towards society and the environment, the...

Select how often (in days) to receive an alert: Senior Clinical Research Physician Non-Obstructive Respiratory Diseases Department: Global Clinical Development Business Area: 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...

Who we are looking for This is what you will do Strategic leadership role within Global Clinical Development, responsible for overseeing Data Management, Biostatistics, and Statistical Programming functions. The position drives the vision, execution, and innovation of clinical data strategies across all phases of drug development, ensuring scientific rigor, operational efficiency, and regulatory...

Business Area: 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 90 years’ experience, operating in 31 countries with more than 7,000 employees (Chiesi Group). To achieve its mission of improving people’s quality...

Location: Europe - Remote, IT About us Based in Parma, Italy, Chiesi is an international research-focused pharmaceutical and healthcare group with 90 years’ experience, operating in 31 countries with more than 7,000 employees. To achieve its mission of improving people’s quality of life by acting responsibly towards society and the environment, the Group researches, develops and markets...

Select how often (in days) to receive an alert: Senior Director, Clinical Biometrics & Analytics Department: Global Clinical Development Business Area: 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 90...