• 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...
...Commitment: 12 months
Education: Bachelor's/Master's in agriculture, economics, social sciences or related fields
Organization: J-PAL South Asia at IFMR
Company description: J-PAL South Asia at the Instit...
Job Title:
Clinical Data Associate
Job Location: Trivandrum, Kerala
Job Overview:
The Clinical Data Associate assists the Clinical Data Manager with the process of cleaning and validating data in clinical trials in accordance with Clinipace SOPs, ...
Clinical Research Associate II / Senior CRA - Cardiology
The Clinical Research Associate is the person in Trial Coordination and Site... ...strategic resourcing and FSP services to the biopharmaceu...
...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...
Clinical Research Associate II / Senior CRA CardiologyThe Clinical Research Associate is the person in Trial Coordination and Site Management that serves as primary contact point between the sponsor and the investigational site. This position is assi...
Are you looking to kickstart a purposeful and rewarding Medical Writing career
Our Oncology Medical Writing team is growing in India, and with big ambitions and a clear vision for the future, now is the time to join Clari...
...integrity of the subject data in the clinical trial database under Risk Based Monitoring (RBM) mode. The areas of activity include but... ...reviewing study data in the system for the signal ...
...members during study lifetime, Review of vendor related protocol sections during protocol development. Collaborate with Vendor startup manager to the development of Study Specification Worksheet (SSW) to facilitate ...
