Kuwait Jobs Today: Ora Company announces new job opportunities. Are you
looking for job opportunities in Kuwait? Ora Company announces the opening of
recruitment for many jobs in various specializations in Kuwaiton today's date.
These opportunities are available to all nationalities. Learn about the
available jobs and how to apply through the following advertisement.
Required jobs in Ora company and their details:
Clinical Document Quality Specialist II
About the job
POSITION TITLE: Clinical Document Quality Specialist II
DEPARTMENT: Ora Europe
LOCATION: Remote - UK, Italy or Spain
Ora Values the Daily Practice of …
Prioritizing Kindness * Operational Excellence * Cultivating Joy * Scientific
Rigor
At Ora, we are building the future of ophthalmic clinical research. As the
world’s leading full-service ophthalmic drug and device development firm, we
guide our clients across all phases of clinical research to efficiently bring
new products and therapies to market. Over the past forty years, our expert
teams have helped earn more than fifty new product approvals. Today, our team
continues to expand across the globe, with over 350 employees across the US,
Europe, Australia, and Asia.
The Role:
Ora’s Clinical Documentation Quality Specialist II (CDQS II) is responsible
for the management, quality and oversight of the electronic Trial Master File
(eTMF) associated with all phases of assigned clinical trials (i.e., set-up
through final transfer / archival).
CDQS II’s are crucial for ensuring Ora’s clinical teams operate in compliance
with SOPs and processes, study sponsor expectations and all applicable
regulations.
This role will focus on the oversight of quality of documents being uploaded
to the eTMF and monitoring compliance to the TMF relative to inspection
readiness and handle such issues independently and with oversight for
escalations as needed.
Additionally, our CDQS II’s have the responsibility of preparing documentation
required for regulatory agency inspections and internal audits.
This role reports directly to the Clinical Document Quality Manager while
working in collaboration with various clinical study teams such as Quality
Assurance, Chemical Manufacturing Control, and Medical Devices.
Ora’s CDQS II’s will train to become Veeva Vault Super Users and be
responsible for providing support and training to department team members
including Clinical Trial Associates (CTAs) and Clinical Research Associates
(CRAs) as well as more junior members of the CDQS team, identify process
improvements, handle escalations for documentation resolutions.
How to apply for jobs
To apply for the aforementioned jobs, you can follow these steps:
To go to the application page. (
Job opportunities for Ora Company
)
Click on a job title to view details.
Please click the Easy Apply button at the top of the page.
Enter the required information in the pop-up screens.
Click Review to review the form.
Source and additional details
Job source: The official website of the company
Posted Date: 23-12-2023 (Please check the date before applying).
Required Nationalities: All nationalities.
23 ديسمبر 2023