Clinical Site Manager (CSM)
... . You will partner with the Clinical Trial Lead (CTL,) Clinical Trial Manager (CTM,) Clinical Trial Specialist (CTS,) and Study Start-Up Specialist (SSS) to ...
... . You will partner with the Clinical Trial Lead (CTL,) Clinical Trial Manager (CTM,) Clinical Trial Specialist (CTS,) and Study Start-Up Specialist (SSS) to ...
... Coordinator to join our vibrant Clinical Operations team in Munich. This is a fantastic opportunity to work on pre-award and post-award study feasibilities, build and maintain strategic ...
... care. The Opportunity: As a Study Start-Up Specialist you will be a local expert in Study Start Up (SSU) activities and strategy including the use of various clinical systems (e.g., CTMS) to ...
... key business stakeholders (e.g., study teams) to support the timely completion of both drug and non-drug program goals and objectives. Your role sits within Clinical Operations Excellence (COE). Key Responsibilities ...
... of data (e.g., clinical study results, post-market surveillance data, ... ., ICMJE). Strong knowledge of clinical research methodology, including study design, outcomes and measures, and ... of direct experience in clinical evaluation report writing in the ...
... haematology), as well as supported study (including rounds, Journal club etc.). The prospective candidate will receive training in all fields of Clinical Pathology including haematology, cytology, clinical chemistry, urinalysis and laboratory quality ...
... key business stakeholders (e.g., study teams) to support the timely completion of both drug and non-drug program goals and objectives. This role sits within Clinical Operations Excellence (COE). This position ...
... opportunity for you Our successful Clinical Research Associates possess varied backgrounds ... - MEDPACE CRA TRAINING PROGRAM No clinical experience is needed as Medpace ... may also participate in other clinical research departmental core rotations, learning ...
... site staff including coordinators, clinical research physicians and their site ... with the protocol; Assessing the clinical research site’s patient recruitment and ... record of demonstrating experience in clinical patient management, protocol, CRF, preparing ...
... professionals to support clinical trial delivery. In this role, you will be responsible for initiating, monitoring, and closing out study sites, ensuring compliance with protocols, ... compliance standards. Update Clinical Trial Management Systems (CTMS) and ...