Study Start Up Associate Jobs in Colorado (NOW HIRING)

Study Start-Up/Regulatory Submissions experience within a CRO is required. Incentives can include: Competitive bonus program, sign-on/relocation bonus, and equity awards. Location: Position can be ...

Maintain timelines for study start-up through both internal and external collaboration; * Provide ... associates, as well as those that are new to the industry. The SAM Training Program embraces ...

Maintain timelines for study start-up through both internal and external collaboration; * Provide ... associates, as well as those that are new to the industry. The SAM Training Program embraces ...

Senior Clinical Research Associate As Clinical Research Associate you will be responsible for ... Works with Study Start-up Group and site staff to obtain regulatory (IRB/EC) approval of study ...

Senior Clinical Research Associate As Clinical Research Associate you will be responsible for ... Works with Study Start-up Group and site staff to obtain regulatory (IRB/EC) approval of study ...

This role will coordinate day-to-day research operations for faculty and students; facilitate compliant and efficient study start-up and execution; maintain research documentation and reporting; and ...

Partners seamlessly with internal teams (e.g., Medical Affairs, Study Start-Up) and CROs to ensure unified site communication, while maintaining meticulous documentation of site visits and ...

This role will coordinate day-to-day research operations for faculty and students; facilitate compliant and efficient study start-up and execution; maintain research documentation and reporting; and ...

This role will coordinate day-to-day research operations for faculty and students; facilitate compliant and efficient study start-up and execution; maintain research documentation and reporting; and ...

Manage all clinical study project elements from initiation to close-out with an emphasis on study start-up ensuring training and education of investigators and research staff. * Work collaboratively ...

Support study start-up and planning, including PSVs and SIVs * Support IRB submission and correspondence * Facilitate monitoring visits (IMVs) and sponsor correspondence including managing the ...

... for study start up * Manage scheduling and coordination of subject study specified treatment, follow-up visits and procedures. Manage collection of data from source documents pertaining to study ...

... for study start up * Manage scheduling and coordination of subject study specified treatment, follow-up visits and procedures. Manage collection of data from source documents pertaining to study ...

Updates study start up checklists to reflect tasks completed. * Develops standard operating procedures for the pharmacy department to comply with company and regulatory requirements. * Supports and ...

CReST provides a la carte support services to clinical investigators for all activities related to the successful conduct of clinical research, from study start-up through close out. This is the ...

CReST provides a la carte support services to clinical investigators for all activities related to the successful conduct of clinical research, from study start-up through close out. This is the ...

Manage all clinical study project elements from initiation to close-out with an emphasis on study start-up ensuring training and education of investigators and research staff. * Work collaboratively ...

... study start-up and close-out. Team Collaboration (20%) * Communicate and collaborate with various colleagues (e.g., principal investigator, clinicians, medical staff, sponsors, contract research ...

... study start-up and close-out. Team Collaboration (20%) * Communicate and collaborate with various colleagues (e.g., principal investigator, clinicians, medical staff, sponsors, contract research ...

May support start-up phase. Ensure copies/originals (as required) site documents are available for ... Collaborate and liaise with study team members for project execution support as appropriate.