Reporting to the Senior Director, Clinical Trials Office, the Associate Director, Clinical Trials Operations is responsible for the overall management and oversight of the assigned Clinical Research Disease group managers. The Associate Director oversees all clinical trial operations activities, has...
The Clinical Trial Associate (CTA) will support the clinical trial team, ensuring that all essential documentation is collected, maintained and filed during the study. Collaborate with Clinical Trial Manager(s) to assist in the operational and logistical aspects of clinical trial management tasks (e...
The Associate Director, Clinical Trial Oversight will manage Clinical Trial Oversight Leads (CTOLs) and direct the work of FSP CTOLs. Associate Director, Clinical Trial Oversight will provide strong leadership and clinical operations experience to support Alnylam's oversight of CRO monitoring effect...
Associate Director- Clinical Trial Management. You will independently lead our clinical study, including planning, maintaining timelines and budgets, vendor management, relationship management between clinical sites and vendors, management of clinical sites, liaise with internal and external collabo...
This individual will assist the Clinical Trial Lead and the clinical team in the day-to-day operations, set-up, execution, and closeout of assigned trials. The individual is accountable to the clinical trial team for the support of trial execution and works collaboratively with cross-functional team...
Knowledge of the Pharmaceutical Industry Clinical trial process (clinical trial conduct, documentation and reporting) in accordance with ICH/GCP and other regulatory compliance guidelines. Creates a documentation system chronicling all incoming/outgoing clinical documentation, maintains study supply...
Serves as a member of the clinical operations team and provides administrative support and tracking of trial status, with the goal to contribute towards efficient management of trials. Our lead investigational product candidate, ninerafaxstat, has completed Phase 2 clinical trials in non-obstructive...
Knowledge of the Pharmaceutical Industry Clinical trial process (clinical trial conduct, documentation and reporting) in accordance with ICH/GCP and other regulatory compliance guidelines. Creates a documentation system chronicling all incoming/outgoing clinical documentation, maintains study supply...
Serves as a member of the clinical operations team and provides administrative support and tracking of trial status, with the goal to contribute towards efficient management of trials. Our lead investigational product candidate, ninerafaxstat, has completed Phase 2 clinical trials in non-obstructive...
Clinical Trial Associate (CTA) position will assist with daily clinical trial execution activities including enrollment management, vendor oversight, and the coordination of documents associated with the conduct of investigational clinical studies in accordance with applicable regulations, Good Clin...
Associate Director- Clinical Trial Management. You will independently lead our clinical study, including planning, maintaining timelines and budgets, vendor management, relationship management between clinical sites and vendors, management of clinical sites, liaise with internal and external collabo...
Clinical Trial Associate (CTA) position will assist with daily clinical trial execution activities including enrollment management, vendor oversight, and the coordination of documents associated with the conduct of investigational clinical studies in accordance with applicable regulations, Good Clin...
The Clinical Trial Associate (CTA) will administer, maintain, and coordinate the logistical aspects of clinical trials and participate in a variety of clinical activities to support and facilitate the efficient conduct of Agios’ clinical research programs. Clinical Trial Associate, Clinical Operatio...
The Associate Director, Clinical Trial Oversight will manage Clinical Trial Oversight Leads (CTOLs) and direct the work of FSP CTOLs. The Associate Director, Clinical Trial Oversight will provide strong leadership and clinical operations experience to support Alnylam’s oversight of CRO monitoring ef...
This role will process clinical documents for anonymization and/or pseudo anonymization in support of Health Canada's PRCI process, EMA policy 0070, EU Clinical Trial Regulation (CTR) and other disclosures of clinical documents that must be redacted or otherwise anonymized to support results posting...
Responsibilities Responsible for managing CROs/vendors for assigned trials ensuring adherence to defined scope of work and budget Identify issues and implement solutions to ensure timelines are maintained Organize/maintain tracking systems and tools to support the conduct of a clinical study from st...
In large complex trials the Associate Clinical Trial Physician helps the Clinical Trial Phyician to maintain the reliable, high quality real time medical oversight. As delegated by the Global Clinical Trial Physician: may contribute to review of study protocols and amendments, Clinical Study Reports...
Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications – from discovery to reality. ...
This role will process clinical documents for anonymization and/or pseudo anonymization in support of Health Canada’s PRCI process, EMA policy 0070, EU Clinical Trial Regulation (CTR) and other disclosures of clinical documents that must be redacted or otherwise anonymized to support results posting...
Clinical Trial Associate (CTA) position will assist with daily clinical trial execution activities including enrollment management, vendor oversight, and the coordination of documents associated with the conduct of investigational clinical studies in accordance with applicable regulations, Good Clin...
The Clinical Trial Associate (CTA) will support the clinical trial team, ensuring that all essential documentation is collected, maintained and filed during the study. Collaborate with Clinical Trial Manager(s) to assist in the operational and logistical aspects of clinical trial management tasks (e...
Associate Director- Clinical Trial Management. You will independently lead our clinical study, including planning, maintaining timelines and budgets, vendor management, relationship management between clinical sites and vendors, management of clinical sites, liaise with internal and external collabo...
Reporting to the Senior Director, Clinical Trials Office, the Associate Director, Clinical Trials Operations is responsible for the overall management and oversight of the assigned Clinical Research Disease group managers. The Associate Director oversees all clinical trial operations activities, has...
The Clinical Trial Associate (CTA) will support the clinical trial team, ensuring that all essential documentation is collected, maintained and filed during the study. Collaborate with Clinical Trial Manager(s) to assist in the operational and logistical aspects of clinical trial management tasks (e...