Senior Associate Study Manager - Blue Bell

We're proud to foster an inclusive environment driving innovation and excellence, · Assists the SM Study Lead and study team with the operational conduct of clinical studies, ...

The job involves assisting the SM Study Lead and study team with the operational conduct of clinical studies. Key responsibilities include planning and tracking clinical supplies, managing lab specimens, and interacting with internal and external stakeholders for support of clini ...

We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. · ...

The Study Manager assists the SM Study Lead and study team with clinical studies. · Operational conduct of clinical studies. · Laboratory specimen tracking. · ...

Sr Study Manager - Oncology - Home Based (US or Canada) · BS/BA/MS/PhD with 7+ yrs clinical research experience · ...

We're proud to foster an inclusive environment driving innovation and excellence, · and we welcome you to join us on our mission to shape the future of clinical development.What You Will Be Doing · Work with the clinical trial management staff to support the execution and monitor ...

We're proud to foster an inclusive environment driving innovation and excellence. · ...

We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.Work with the clinical trial management staff to support the execution and monitoring of clinical studies and ...

This role supports Lead Epi Scientists by providing operational support for study conduct. It involves coordination and execution of observational research studies in compliance with Good Pharmacoepidemiology Practice (GPP) and Standard Operating Procedures (SOPs). The Senior Stu ...

The Senior Study Manager will provide overall operational support for study conduct. · The team pushes the boundaries of global healthcare through research and innovation.Through clinical trials and surveillance, we ensure the safety and efficacy of our existing and pipeline prod ...

+Operational planning · and project management of epidemiology research studies+ · +Execution, · close out of primary data collection,+chart review database, · molecular epidemiology studies in addition to other activities+ · +Manage vendors including qualification efforts confid ...

May lead or support a study or studies, depending on size/complexity. · ...

As a Country Study Operations Manager at ICON plc, you will be responsible for overseeing study and regional/country level activities from startup through conduct and close. You will manage the study start up process in countries assigned and oversee the Site Care Partner/Country ...

+We are currently seeking a Manager, Study Start-Up to join our diverse and dynamic team. · + · Responsibilities · Managing and overseeing the end-to-end study start-up process, including site identification, feasibility, regulatory submissions, and site activation. · Leading a t ...

We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. · We will be working with the clinical trial management staff to support the execution and monitoring of cli ...

This role within GCSD plays a pivotal part in driving clinical operations of assigned studies from Commit to Study Initiation (CSI) all the way through study archiving As Global Study Manager (GSM) you'll craft robust accelerated delivery plans ensuring timelines quality standard ...

This role within GCSD plays a pivotal part in driving the clinical operations of assigned studies. The Global Study Manager will take ownership of crafting robust delivery plans that aim for top-tier performance. · GSM will be the Working Group (WG) Lead for Clinical Operations w ...

The Associate Director, Clinical Study Management will lead end-to-end execution of clinical trials-primarily in oncology, · with flexibility to support additional therapeutic areas as needed.You'll provide day-to-day leadership to cross-functional study teams, · ensure delivery ...

The Senior Clinical Trial Associate will support all phases of clinical trial activities under the direction and supervision of Clinical Operations Lead(s). Plans, supports, and communicates clinical trial timelines. Ensures consistency of processes across clinical trials. · Bach ...

We have an incredible opportunity for a Manager, Site Resourcing to join ICON's Site Resourcing team. · The Manager, Site Resourcing will drive the development and execution of Accellacare Site Resourcing for future and awarded study needs by aligning and executing Sponsor requir ...