Sr Clinical Trial Coordinator - Logistics

Detalles de la oferta

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe. Responsibilities:  · Serve as contact for project team and investigative sites, conduct site contacts and document contacts for assigned sites as required per study guidelines, including creating contact reports for each telephone session (outbound or inbound) with sites.  Monitor site performance and implement action plans for sites not meeting expectations, in conjunction with the CRA.  Assist CRAs with preparation for site visits (i.e. running reports, QC of files (checking for missing documents), resolving action items from previous visits).  Perform Case Report Form review, query generation and resolution against established data review guidelines, under direct supervision on Covance or client data management systems, as assigned by management.  Assist with the coordination of study visits and shipment of drug, ancillary supplies and laboratory kits/samples.  Manage sites to ensure subjects are complying with protocol requirements, study visits, and timelines.  Liaise with the project team and others to distribute and track clinical trial supplies, e.g. Case Report Forms, study medication, lab kits, ensuring that sites have sufficient supplies to continue recruitment.  Proactively work with sites and project teams to ensure maintenance activities (including Amendments, revised documents, etc.) are completed for assigned sites as applicable in region.  Demonstrate an understanding of the purpose of CTMS, how to use it, and how to navigate within the different sections. To enter weekly details in CTMS or as per study requirement.  Assist in submissions and notifications to Ethics Committees and Regulatory Authorities as applicable in region.  Facilitate translation and back translation of all necessary documents as appropriate for local country requirements and as needed regionally.  Attend, as needed, meetings (investigator, sponsor, kick-off, face-to-face) and to present at the meetings.  Education BA (Life Science preferred) Requirements:    Previous experience with Logistics / Imports / Supplies within CRO enviroment Completed job training (office management, administration, finance, health care preferred) or Bachelor's Degree. Advanced English Good IT skills (Use of MS office and Strong MS Excel skills required) Hands-on profile Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact.


Salario Nominal: A convenir

Fuente: Whatjobs_Ppc

Requisitos

Líder De Investigaciones

El Consejo Nacional del Trabajo Social (CNTS) se encuentra en la búsqueda de un Líder de Investigación para fortalecer sus proyectos y estrategias investigat...


Desde Consejo Nacional De Trabajo Social - Cundinamarca

Publicado 20 days ago

Desarrollador De Negocios

Únete a nuestro equipo, estamos buscando un Desarrollador de negocios con mas de 2 años de experiencia en venta de soluciones de TI. Tecnólogo o técnico o In...


Desde Redneet Sas - Cundinamarca

Publicado 18 days ago

Bussines Development Cro (Clinical Research) At Integra It

We (Torre) are helping Integra IT find a top candidate to join their team full-time for the role of Bussines Development CRO (Clinical Research). Compensatio...


Desde Independent Recruiter - Cundinamarca

Publicado 18 days ago

Analista De Seguridad Y Salud En El Trabajo

Empresa del sector floricultor requiere Profesional en Seguridad y Salud en el Trabajo con experiência mínima de 1 año para el cargo de Analista SST. Horari...


Desde Agrícola Cunday Sas - Cundinamarca

Publicado 18 days ago

Built at: 2024-11-06T03:03:37.616Z