Resultados de la búsqueda: 10 vacantes
...manager for clinical operations.
• Manages and prioritizes the clinical deliverables to ensure that deliverables meet quality and regulatory requirements, project timelines, budget, and sponsor expectations.
• Creates and administers clinical and site training plans....
Trabajo remoto
...user onboarding and account management across our suite of services. These include KYC/AML processes, entitlements management and regulatory reporting. The team is instrumental in ensuring a compliant and efficient user onboarding experience, enabling over a million...
...Research Experience required, including at least 2 years of experience in Clinical Trial ;anagement.
~ Knowledge of ICH and local regulatory authority applicable regulations.
~ Read, write and speak fluent English; fluent in host country language required.
~...
Trabajo remoto
...terms and pricing.
Ensure contracts are accurately documented, tracked, and maintained in accordance with company policies and regulatory requirements
Invoice Management:
Oversee the end-to-end invoice management process, including receipt, verification, and...
Trabajo remoto
...in accordance with the Sponsor and/or PRA protocol, standard operating procedures (SOPs), ICH/GCP guidelines and all applicable regulatory requirements. At the Senior level, the Study Start Up Associate will manage and lead all activities listed above and will ensure...
Trabajo remoto
...yearly budget for your individual learning and development goals.
At Xapo, we prioritize consumer protection and adhere to regulatory requirements by ensuring that all Xapiens are accountable for upholding principles of fair treatment, transparency, and ethical conduct...
...creating, documenting & refining the SW engineering process
Nice to Have
Life sciences domain knowledge, especially the regulatory area
Experience with Atlassian products like Jira
Manage a platform QA team
Manage an applications development QA team...
...most successful clinical trial possible. You will lead cross-functional teams with Project Management, Clinical Operations, and Regulatory Affairs, while understanding and managing client expectations. You will proactively identify, resolve/mitigate, and escalate risks...
Trabajo remoto
...investigative sites. Initiates clinical trial sites according to the relevant procedures to ensure compliance with the protocol and regulatory and ICH GCP obligations, making recommendations where warranted. Ensures trial close out and retrieval of trial materials.
...
Trabajo remoto
...standard operating procedures (SOPs), International Conference on Harmonization Good Clinical Practices (ICH-GCP) and all applicable regulatory requirements.
Main activities
• Completes onsite and remote monitoring activities in accordance with all ICH-GCP...
Trabajo remoto
