...Job Title: Medical Content Reviewer
Location: Hyderabad, Telangana
Job Type: Full-time (on-site)
Job Overview:
We are seeking an experienced and detail-oriented Medical Content Reviewer with minimum 5-6...
...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...
...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...
...we can help you build the career you want - developing your skills, working on challenging problems, to ultimately develop clinical therapies that matter
Provide project and technical support in the preparation, ...
...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...
