: Develops, executes and maintains high impact territory plans, including HCP and Investigator engagement plans in alignment...&D to include, but not limited to, site evaluation and identification, recruitment, investigator meetings, external expert...
: Under supervision may collect information about AEs, identified in the protocol or investigator brochure. Conducts and documents consent...
, identified in the protocol or investigator brochure, and reports to study team. Conducts and documents consent for participants...
Organizations (AROs), and meetings with CRO and Investigator Meetings. Support Fair Market Value process in evaluating study...-up, Investigator/site performance, recruitment, regulatory documents, TMF filing and QC activities and elevate areas...
proposals; monitors grant expenditures and advises principal investigator of changes in reporting or accounting requirements...
responsibilities include: Effectively function as a principal investigator, generating original technical ideas and research...
and storage. Assists in developing and submitting grant proposals; monitors grant expenditures and advises principal investigator...
and storage. Assists in developing and submitting grant proposals; monitors grant expenditures and advises principal investigator...
and edit clinical development documents, including but not limited to, clinical protocols, investigator’s brochures, clinical...
and edit clinical development documents, including but not limited to, clinical protocols, investigator’s brochures, clinical...
and edit clinical development documents, including but not limited to, clinical protocols, investigator’s brochures, clinical...
but not limited to, clinical protocols, investigator’s brochures, clinical study reports, subject consent forms, integrated safety...
but not limited to, clinical protocols, investigator’s brochures, clinical study reports, subject consent forms, integrated safety...
, but is not limited to, investigator’s brochures, clinical study reports, subject consent forms, integrated safety and efficacy summaries...
, but is not limited to, investigator’s brochures, clinical study reports, subject consent forms, integrated safety and efficacy summaries...
and edit clinical development documents, including but not limited to, clinical protocols, investigator’s brochures, clinical...
, but is not limited to, investigator’s brochures, clinical study reports, subject consent forms, integrated safety and efficacy summaries...
, but is not limited to, investigator’s brochures, clinical study reports, subject consent forms, integrated safety and efficacy summaries...
, but is not limited to, investigator’s brochures, clinical study reports, subject consent forms, integrated safety and efficacy summaries...
but not limited to, clinical protocols, investigator’s brochures, clinical study reports, subject consent forms, integrated safety...