Study Activation Jobs (NOW HIRING)

Study preparation, activation, and close-out responsibilities * Follow up, maintenance, and reporting * Time management, planning, and coverage support Education Bachelor's Degree Required Other ...

Following study activation, the role will transition to 1 day per week and is expected to grow to 2-3 days per week as the site expands and additional studies are activated. * Location: Springfield ...

This process will take place from study activation throughout the completion of the study. * Preparation and maintenance of regulatory binders (paper or electronic) with all necessary study ...

Following study activation, the role will transition to 1 day per week and is expected to grow to 2-3 days per week as the site expands and additional studies are activated. * Location: McAllen, TX ...

Following study activation, the role will transition to 1 day per week and is expected to grow to 2-3 days per week as the site expands and additional studies are activated. * Location: Springfield ...

Drive efficient research contracting processes to reduce study activation timelines. Collaborate closely with OneR's budgeting, regulatory, study activation, and other teams on any cross-functional ...

The position will work closely with the members of the clinical research team to develop effective tools for close monitor and reporting of trials accrual and coordinate the timely study activation ...

This process will take place from study activation throughout the completion of the study. * Preparation and maintenance of regulatory binders (paper or electronic) with all necessary study ...

First POSITION RESPONSIBILITIES Oversight of a clinical study including enrolment, long-term follow-up, trial master file maintenance and study activation phases. Ensure site compliance in regulatory ...

... study activation timelines. • Collaborate closely with OneR's budgeting, regulatory, study activation, and other teams on any cross-functional matters and to ensure visibility on contract timelines ...

The Director serves as a key business partner across Clinical Study Leadership, Regulatory, Clinical Site Management, and other stakeholders to accelerate study activation while maintaining ...

Supporting protocol activation activities by tracking required intake documents, organizing study files, maintaining study records, and facilitating communication among internal and external ...

... study activation, providing study guidance and support throughout the trial lifecycle. * Participate in internal and external meetings, including site calls and sponsor touchpoints, to provide ...

Ensure smooth implementation of new trials from conception through study activation. * Monitor, track, and report critical study start-up milestones e.g., IRB activities, processing and finalization ...

Support study activation, maintenance, and closeout activities within the CTMS. * Monitor data quality and resolve discrepancies in a timely manner. * Ensure compliance with institutional policies ...

The position will work closely with the members of the clinical research team to develop effective tools for close monitor and reporting of trials accrual and coordinate the timely study activation ...

... study activation, providing study guidance and support throughout the trial lifecycle. * Participate in internal and external meetings, including site calls and sponsor touchpoints, to provide ...

Collaborate with the Protocol Activation office to initiate and activate new clinical trial protocols using established study start-up task lists. * Prepare and review study tools such as study ...

... site activation for study subject enrollment. * Oversee site compliance with investigational products, reporting or safety events and contracting. * During trial implementation, oversee site ...

The position emphasizes accuracy, responsiveness, and learning institutional best practices to support efficient study activation. ESSENTIAL FUNCTIONS * Contract Review & Processing: Reviews, routes ...