• Close interaction and collaboration with study team lead and study team members during study lifetime, Review of vendor related protocol sections during protocol development. Collaborate with Vendor startup manager to the development of Study Speci...
...Study Design: The Clinical Research Associate would be expected to:
Assist with the identification and selection of investigators to... ...and guidelines in the relevant regions.
Basic...
...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...
1) Act as DRLs direct contact with assigned sites, assess and ensure overall integrity of study
2) Implementation and adherence to study protocol at clinical investigational sites, and resolve site issues. Escalate issues that were unresolved to ...
...project that matches the organization's vision and is suitable for broadcasting Prakara through the app.
Core Functions:
Creating Motion Graphics in Adobe After Effects and Adobe Premiere.
Utilizing Phot...
...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...
A person who is extremely passionate about Business Development and Sales in the Education sector and has excellent Conversion skills.
Responsibilities:
Your role will start with contacting potential customers (parents and students) to counsel ...
Secunderabad
Quality Thought Infosystems (India) Private Limited
Salary
up to 8lpa for UK Counselor
Canada - 6.5 lpa
USA up to 8lpa
Experience: Minimum 1 year
Immediae Joiner
Key Responsibilities... ...communication, and program management.
Kno...
...log/trial allocations forms, site and vendor contact lists, drug shipping logs, set up and maintenance of team membership and contact... ...delegated aspects of trial data analysis and report...
