... for all study plans. - Ensure the availability and maintenance of all essential documents in accordance with ICH GCP throughout the study. - Support and assist CRAs with project-specific matters. Ensure all study stakeholders receive proper training throughout the study. - Perform vendors selection and management. - Collaborate ...
... attention to detail - Knowledgeable on setting up Contracting Plans - Guides for CTA & Budget negotiations - Successful handling relationship study team and/or with CRAs/Start-up Associate/(S)BSCA to meet study timelines Skills and Competencies - Possesses strong organizational/written communication skills and the ability to multi-task ...
... attention to detail - Knowledgeable on setting up Contracting Plans - Guides for CTA & Budget negotiations - Successful handling relationship study team and/or with CRAs/Start-up Associate/(S)BSCA to meet study timelines Skills and Competencies - Possesses strong organizational/written communication skills and the ability to multi-task ...
... not your typical CRO. We are passionate about cultivating our culture and are proud to share extremely high CRA retention rates compared to industry averages. CRAs join us, love their jobs, and stay because of the amazing people and enjoyable quality of life. You will have a lower than average number of protocols, setting ...
The Collecting Group is a true disruptor, offering high-quality ‘curated collectibles' from around the globe, curated by specialists in their subject matter. It has headquarters in London, and offices in Munich, Sydney and Stockholm, as well as a strategic partnership in the UAE.
IQVIA in Barcelona is seeking a Senior Clinical Research Associate to join our sponsor-dedicated CRA team. You will support multicenter trials, perform site visits, and help ensure GCP/ICH compliance throughout study conduct.
En SQUAD Technology Solutions , una compañía de outsourcing tecnológico, estamos construyendo un con un fuerte compromiso por hacer las cosas bien desde el principio.
Position: QA Specialist (PRD) – Investigations, CRs, CAPAs & Floor Oversight Location: León (on-site) Experience: At least 3 years’ experience in similar roles within the Quality department in pharmaceutical industrial settings Want to find out more?
... policies, SOPs, ICH-GCP guidelines, regulatory requirements, and contractual obligations. You will work closely with Project Managers, Clinical Research Associates (CRAs), sponsors, and investigative sites to ensure studies are delivered on time, within scope, and to the highest quality standards. Key Responsibilities - Manage ...
... this, it will investigate the use of scrap tolerant or low carbon aluminium alloy products, either stamped or extruded, for EV specific and armour components in crashworthiness and impact scenarios aiming to reduce the GHG emissions. To achieve this target, and to tackle the afore-mentioned challenges we will: - Assess the ...