States Basking Ridge, USA Posting date: 01 Oct 2024 Reference: 62532 Senior Manager of Clinical Study Lead - Contract... - Basking Ridge NJ Proclinical is seeking a Senior Manager, Clinical Study Lead to oversee and manage clinical study...
The Senior Clinical Study Lead (CSL) is expected to operate with high-degree of independence and is accountable for the... global execution of assigned large and/or complex clinical trials from study design, through execution, to study close out...
The Senior Clinical Study Lead (CSL) is expected to operate with high-degree of independence and is accountable for the... global execution of assigned large and/or complex clinical trials from study design, through execution, to study close out...
The Senior Clinical Study Lead (CSL) is expected to operate with high-degree of independence and is accountable for the... global execution of assigned large and/or complex clinical trials from study design, through execution, to study close out...
. The Clinical Study Manager-4 (CSM IV) role will develop and execute strategies for clinical and outcomes research studies... and drive study meetings and other study activities as assigned Mentor junior clinical study manager(s); provide guidance...
of a larger study. Forecast and manage the Clinical Trial Budget for the program. Provide country and regional level input... for patients. What You Will Achieve You will be part of Pfizer's medical team and manage obesity clinical studies. Your project...
that the clinical studies are within time, budget and scope. As a Senior Manager, your advanced knowledge of the principles... plans. Resolve escalated issues identified by the site activation sub team in partnership with the Study Operations Manager...
Our mid-sized medical device client is adding a Clinical Study Manager to the team! The Clinical Study Manager... will report to the Sr. Clinical Manager and will oversee clinical activities related to one or more clinical studies...
The Sr. Project Manager of the Research Site (PMRS) is responsible for oversight of all operational aspects of the TIMI... oversight of all phases of clinical research, including study activation, enrollment, follow up, and closure. The (PMRS...
The Sr. Project Manager of the Research Site (PMRS) is responsible for oversight of all operational aspects of the TIMI... oversight of all phases of clinical research, including study activation, enrollment, follow up, and closure. The (PMRS...
skills to successfully lead a clinical study team Ability to deal with time demands, incomplete information or unexpected... and commercialization of Gilead’s products. EXAMPLE RESPONSIBILITIES: In partnership with Clinical Program Manager or Associate Director...
for one or more trials with the necessary supervision May co-lead study team meetings in partnership with GDO protocol manager... and presenting protocol documents, conducting literature reviews, monitoring clinical data, and contributing to clinical study...
for one or more trials with the necessary supervision May co-lead study team meetings in partnership with GDO protocol manager... conduct May serve as Clinical Trial Lead for one or more trials May lead or support trial level activities...
, and problem-solve. We are currently hiring a Clinical Data Manager II or Senior Clinical Data Manager to join our team! You'll... supports study outcomes; proactively clean clinical trial data and mitigate risks; effectively communicate data-related...
standard library; lead and perform sponsor acceptance testing of the clinical database. Contribute to the development/review...Responsibilities: Act as the point of contact for DM activities for the assigned clinical studies and proactively...
(include, but are not limited to): Primary - Good Clinical Practice (“GCP”) Audit Management: Lead, plan, conduct.../regulatory requirements and guidelines, study protocols, monitoring plans, and applicable policies/procedures. Develop and lead...
Responsibilities: Effectively plan and execute Data Management projects from study start-up to database lock. Serve.... Lead, coordinate, and perform User Acceptance Testing (UAT) tasks for complex studies and modules. Communicate with cross...
to archival with at least 5 years in lead role for clinical development programs with medical devices leading toward FDA filing... development, validation, and management of the clinical study database throughout its life cycle, from CRF design, database...
planning, organization, conduct, and evaluation of multi-faceted clinical research protocols, including study execution... system. The BTN Coordinator will independently provide clinical research administration and study coordination. The...
procedures, study start-up activities, and internal site initiation visits related to pediatric-patient care clinical research... with prior experience in research, study coordination and clinical experience with patients. JOB-SPECIFIC COMPETENCIES...