Irb Director Remote Jobs (NOW HIRING)

This is a part-time position (approximately 25 hours per month) and is remote within the U.S., with ... Support hospital IRB processes and vendor vetting procedures * Lead clinical training and education ...

May be responsible for site IRB submissions (violations, deviations, severe adverse event reports ... Interact with study participants as directed/required by the protocol and/or study team * May be ...

... Administrative Director, Healthcare PWAC. Duties include*: * Act on behalf of supervisor and ... Support collection, routing for approvals, and tracking of research proposals, data requests, IRB ...

... Administrative Director, Healthcare PWAC. Duties include*: * Act on behalf of supervisor and ... Support collection, routing for approvals, and tracking of research proposals, data requests, IRB ...

Lead or support usability activities such as study design, protocol development, IRB submission ... No direct human factors hands on experience Interview process: 2 rounds of interviews We invite ...

Track information and report data such as call outcomes, limiting factors, etc.; as directed ... Maintain compliance with HIPAA regulations, FDA, GCP, and IRB guidelines, local regulations, and M3 ...

Track information and report data such as call outcomes, limiting factors, etc.; as directed ... Maintain compliance with HIPAA regulations, FDA, GCP, and IRB guidelines, local regulations, and M3 ...

Track information and report data such as call outcomes, limiting factors, etc.; as directed ... Maintain compliance with HIPAA regulations, FDA, GCP, and IRB guidelines, local regulations, and M3 ...

... Schedule As directed by supervisor Remote/Telecommuting No remote/telecommuting opportunity ... Support administrator with the processing of all IRB and regulatory paperwork. Duties will also ...

Track information and report data such as call outcomes, limiting factors, etc.; as directed ... Maintain compliance with HIPAA regulations, FDA, GCP, and IRB guidelines, local regulations, and M3 ...

Performs remote clinical and administrative coordination of clinical trials, investigator-initiated ... Responsibilities include study start-up, IRB submissions, recruitment strategy development and ...

The role will be based in Palo Alto, CA or be remote and reports to the Director, Clinical ... Support central and site IRB/IEC and regulatory submissions, as needed. * Accountable to assist ...

The role will be based in Palo Alto, CA or be remote and reports to the Director, Clinical ... Support central and site IRB/IEC and regulatory submissions, as needed. * Accountable to assist ...

... directing and monitoring work efforts, identifying resource needs, performing quality review, and ... Single-IRB (sIRB) coordination & regulatory submissions: preparing sIRB regulatory packets and ...

The role will be based in Palo Alto, CA or be remote and reports to the Director, Clinical ... Support central and site IRB/IEC and regulatory submissions, as needed. * Accountable to assist ...

Direct experience authoring protocols, ICFs, and CRFs * Proven experience managing IRB submissions ... Fully remote work experience * Comprehensive medical, dental, and vision package, including FSA ...

Remote Considered) IVX Health is a national leader in highquality infusion and injection therapy ... Direct, hands-on leadership of clinical trial sites and active studies from startup through ...

Remote locations and work schedules are determined based on operational needs and in consultation ... Reporting to the Senior Associate Director, NU-RES Hub, the Research Administrator works in ...

May be responsible for site IRB submissions (violations, deviations, severe adverse event reports ... Ability to work across satellite locations and provide on-site and remote support * Is competent ...

... IRB processes, HIPAA regulations). Work Conditions & Commitments: • Work hours will vary ... Work may be on-site, hybrid, or remote, depending on project requirements. Restrictions ...