Specialist Study Management - Wilmington

The specialist study management assists in the coordination and administration of the study activities from the start up to execution and close out, · Assists in coordination and administration of clinical studies from the start-up to execution and close-out. · Serves as local ad ...

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 ...

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 ...

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. · We will be working with the clinical trial management staff to support the execution and monitoring of cli ...

The Study Manager is responsible to ensure that quality research is conducted at assigned investigative sites in accordance with the sponsor protocol FDA Regulations and ICH/GCP guidelines. In addition ensure study enrollment meets or exceed Sponsors expectations and company goal ...

The specialist study management assists in the coordination and administration of the study activities from the start up to execution and close out, · Level of education that supports skills and capabilities of the position · Previous administrative experience preferably in the ...

The Senior Clinical Research Associate (Sr. CRA) has local responsibility for the delivery of the studies at allocated sites and is an active participant in the local study team(s). The Sr. CRA works in close collaboration with other teams to ensure that study commitments are ach ...

The Senior Clinical Research Associate (Sr. CRA) has local responsibility for the delivery of studies at allocated sites and is an active participant in the local study team(s). · ...

+ Director Site Management Monitoring The Director Site Management Monitoring DSMM delivers the committed part of all clinical interventional studies under their management p This delivery must accord to agreed resources budget and timelines and must comply with AZ Procedural Doc ...

We are seeking a dedicated Local Study Associate Director to join our dynamic oncology team.In this role, you will lead and manage the study team... · ...

+Job Summary · The Director Site Management & Monitoring delivers clinical interventional studies under their management. · +SUPPORT SMM region in programs/activities. · Evaluate SQV reports of direct reports following AZ SOPs. · ...

The Site Management Associate I (SMA I) is responsible for managing clinical studies with support in a team setting according to ICON SOPs, SSPs and all applicable rules and regulations. · This role involves identifying study sites, conducting remote site monitoring visits, · man ...

Clinical Trial Associate (Clinical Study Administrator). Collects documents for the application process and interfaces with Investigators to support delivery of a study.Operational responsibility for the correct set-up and maintenance of local eTMF including document tracking. · ...

The Senior Staff Scientist, Toxicology position assists with all aspects of set-up and conduct of exploratory pharmacokinetic studies and technical support of toxicology studies conducted in house. · ...

+Candidate must be within commuting distance of Wilmington, DE. · +Monitors progress of clinical trials at the site level or headquarters and ensures that they are conducted... · ...

The Lead Clinical Research Nurse will provide technical guidance and subject matter expertise to facilitate the coordination and conduct of clinical research studies and/or clinical trials within the department/division/unit. · Provides oversight, training, education to research ...

+ The specialist study management assists in the coordination and administration of the study activities from the start up to execution and close out, and within the Local Study Team (LST) to ensure quality and consistency of interventional study deliverables to time, cost and qu ...

The Lead Clinical Research Nurse will provide technical guidance and subject matter expertise to facilitate the coordination and conduct of clinical research studies and/or clinical trials within the department/division/unit. · This individual will play a key role by helping to c ...

The Senior Clinical Research Associate (Sr. CRA) has local responsibility for the delivery of the studies at allocated sites and is an active participant in the local study team(s). · The Sr. CRA acts as the main contact with the study site and has the responsibility for monitori ...