Clinical Trial Assistant - Malvern, PA

The Clinical Trial Assistant plays a crucial role in supporting the Clinical Operations team by managing essential documents in the TMF, developing study materials, and coordinating shipments of clinical trial materials. · Assist in the development, handling, distribution, filing ...

We are seeking a Clinical Trial Assistant to join our diverse and dynamic team at ICON plc. · Assist in the coordination and administration of clinical trials. · Maintain and organize clinical trial documentation. · ...

The Clinical Trial Assistant plays a crucial role in supporting the Clinical Operations team by managing essential documents in the TMF, developing study materials, and coordinating shipments of clinical trial materials. · This role involves communication with sites, CROs, vendor ...

We are seeking a Senior Clinical Associate to oversee and support the execution of clinical trials at ICON plc. · ...

The Site Management Associate I (SMA I) is responsible for managing clinical studies with support in a team setting according to ICON SOPs, SSPs and all applicable rules and regulations. · This role involves identifying study sites, conducting remote site monitoring visits, · man ...

The Clinical Trial Assistant plays a crucial role in supporting the Clinical Operations team by managing essential documents in the TMF. · ...

We are seeking a Senior Clinical Associate to join our diverse and dynamic team. As a Senior Clinical Associate at ICON, you will play a critical role in overseeing and supporting the execution of clinical trials. ...

The Clinical Trial Associate will assist the Clinical Trial Manager in ensuring study planning through completion. · File all clinical trial documentation in (e)TMF and paper TMF, as assigned. · Schedule, prepare and take minutes for the study team meetings. · ...

Promotes company products through education of customers by providing clinical support in areas such as interventional coverage and patient follow-up. · ...

The Clinical Trial Associate will assist the Clinical Trial Manager to ensure study planning through completion. · ...

The Clinical Trial Associate (CTA) will work with the Clinical Trial Manager to ensure study planning through completion. · ...

Cement Field Technical Services Manager leads and executes all external tech services activities including customer production audits product performance assessments new product development studies potential product trials and technical assessment of our productsMaintain alignmen ...

The Staff Accountant will have overall responsibility for preparing all journal entries, account schedules and general accounting for assigned portfolio. · You may be eligible for a $500 net sign on bonus to be paid out in your first paycheck · ...

The Associate Director of Regulatory Affairs - Gene Therapy will support the development and execution of regulatory strategy for Ocugen's gene therapy portfolio. · Contribute to the design and execution of global regulatory strategy for Ocugen's gene therapy programs. · Collabor ...

The Associate Director of Regulatory Affairs – Gene Therapy will support the development and execution of regulatory strategy for Ocugen's gene therapy portfolio. · Contribute to the design and execution of global regulatory strategy for Ocugen's gene therapy programs. · Collabor ...

The Associate Director of Regulatory Affairs – Gene Therapy will support the development and execution of regulatory strategy for Ocugen's gene therapy portfolio. · ...

Cement Field Technical Services Manager leads and executes all external tech services activities. This person will provide expertise in Cement production and Cement Products' raw materials attributes to ensure collaborative and innovative perspectives. ...

· Company Description · Integrated Resources, Inc., is led by a seasoned team with combined decades in the industry. We deliver strategic workforce solutions that help you manage your talent and business more efficiently and effectively. Since launching in 1996, IRI has attracte ...

Manager, Quality Assurance · Full Time · Malvern, PA · OVERVIEW · The Manager, Quality Assurance's primary role is to ensure that all food products produced meet the requirements of customers, standards, regulatory authorities, and the Company. The Manager is responsible for the ...

+Catalent is a leading global contract development and manufacturing organization whose mission is to develop manufacture and supply products that help people live better and healthier lives. · +Perform entry-level micronization and milling of both hazardous and non-hazardous pha ...