... for actively enrolling or planned clinical trials and build relationships with ... awareness about our Client, our clinical trials, our commitment to improving ... to company to help develop clinical as well as commercial strategy. ...
es.talent.com
... for actively enrolling or planned clinical trials and build relationships with ... awareness about our Client, our clinical trials, our commitment to improving ... to company to help develop clinical as well as commercial strategy. ...
es.talent.com
... • Responsible for site management oversight, clinical monitoring and central monitoring deliverables ... . Is accountable for their assigned clinical team members understanding, ongoing compliance ...
es.talent.com
... • Responsible for site management oversight, clinical monitoring and central monitoring deliverables ... . Is accountable for their assigned clinical team members understanding, ongoing compliance ...
es.talent.com
... of Case Report Forms (CRFs), laboratory workbooks, staff requirements, and schedules. ... Monitor appropriate sources for specific clinical study or federal regulation updates. ... Proficiency in use of various clinical trial EDC software preferred. Disclaimer: ...
es.talent.com
... of Case Report Forms (CRFs), laboratory workbooks, staff requirements, and schedules. ... Monitor appropriate sources for specific clinical study or federal regulation updates. ... Proficiency in use of various clinical trial EDC software preferred. Disclaimer: ...
es.talent.com
... medical site staff including coordinators, clinical research physicians and their site staff; Verifying adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff; Medical record ...
es.talent.com
... medical site staff including coordinators, clinical research physicians and their site staff; Verifying adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff; Medical record ...
es.talent.com
... medical site staff including coordinators, clinical research physicians and their site staff; Verifying adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff; Medical record ...
es.talent.com
... , including direct supervision of project Clinical Research Associates and monitoring deliverables ... ; Minimum of 2 years of Clinical Trial Management experience, CRO experience preferred; 5+ years of Project Manager Clinical Trial Manager experience at a ...
es.talent.com