Study Start Up Associate Jobs in Kansas (NOW HIRING)

Accountable for advancing study start-up activities for outsourced trials by understanding the objectives and assisting in the review and approval of the plan for country and site activation. * Laser ...

You will oversee timelines, budgets, operational risks, study start-up activities, vendor performance, and cross-functional collaboration while ensuring studies are conducted in accordance with ...

In this role, you will lead global clinical trials from sourcing strategy and RFP development through study start-up, execution, database release, and inspection readiness-ensuring the timely ...

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 ...

Manage operational aspects of multiple concurrent clinical trials from start-up through close-out, with minimal oversight. * Coordinate and track essential regulatory and study documentation ...

Manage operational aspects of multiple concurrent clinical trials from start-up through close-out, with minimal oversight. * Coordinate and track essential regulatory and study documentation ...

Provide strategic and operational leadership throughout study start-up, conduct, and closeout * Act as the primary point of accountability for study delivery, quality, timelines, and execution * Lead ...

Full lifecyle clinical trial management-from study start-up to close-out. * Business operations knowledge. * Exceptional verbal and written communication skills. * Ability to work independently and ...

Support regulatory components and site research compliance for study feasibility, study start-up, ongoing study monitoring, and site close out. * Provide training and mentorship to clinical research ...

Additional responsibilities include managing adequate study supplies, involvement in coordination of study start-up requirements, assisting with monitor visits and other duties that may be assigned ...

Additional responsibilities include managing adequate study supplies, involvement in coordination of study start-up requirements, assisting with monitor visits and other duties that may be assigned ...

Additional responsibilities include managing adequate study supplies, involvement in coordination of study start-up requirements, assisting with monitor visits and other duties that may be assigned ...

Additional responsibilities include managing adequate study supplies, involvement in coordination of study start-up requirements, assisting with monitor visits and other duties that may be assigned ...

About The Role The Senior Lead Data Manager is responsible for all data management activities from study start-up through database lock and archiving and independently supporting the needs of the ...

Coordinates with the project manager to oversee the scientific aspects of study start-up and ongoing study management. Leads the development of and/or peer-review essential study documents including ...

Coordinates with the project manager to oversee the scientific aspects of study start-up and ongoing study management. Leads the development of and/or peer-review essential study documents including ...

Coordinates with the project manager to oversee the scientific aspects of study start-up and ongoing study management. Leads the development of and/or peer-review essential study documents including ...

About The Role The Senior Lead Data Manager is responsible for all data management activities from study start-up through database lock and archiving and independently supporting the needs of the ...

Lead or support study start-up, site activation, and enrollment , working closely with site monitors, regulatory teams, and contracts personnel. * Serve as a key point of contact across internal (CRO ...

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.