...Submission Teams (CST) to ensure compliance of documentation to internal company standards and external regulatory guidelines.
Program Writer ensuring adequate medical writing resources are available for assigned...
...Align to a regulatory submission strategy in the clinical development part of the projects.
ORGANIZATION STRUCTURE
Reports to: VP - Clinical development
Relationships (Internal): Manager & all other ...
...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 m...
...Our Legal and Compliance Solutions team is looking for Specialist in our Contract Management team who will Individually support and perform contract management related activities for Legal and Business Teams, Compli...
...The Document Coordinator is responsible for managing and executing on centralized activities in support of global trials with an emphasis on clinical documentation.
The Document Coordinator will interact with cli...
...Responsible for Clinical execution and management of all aspects of assigned clinical studies (interventional and non-interventional, from... ...and operational procedures. Might be required ...
...for CT under the EU Regulation.
Position Responsibilities
Manage the signing of clinical trial documentation such as powers of attorney, expected to be able to coordinate many signing at the same time.
Prov...
...to suit different customer personas to drive scanner utilization
He/she also ensures effective, efficient, and prompt handling of doctors inquiries, requests, and complaints regarding the Scanner and CAD/ CAM ava...
Dear Candidates,
We are looking for the below skillset profiles
Must Have:
12+ years of experience in STARLIMS with hands on development experience of 8+ years
Proven Solution architecture and Product Specialist experience – need to guid...
