...Reproting to Associate Director - Medical Writing, Principal Medical Writer is responsible for developing, writing, editing, and reviewing clinical regulatory and scientific writing documents, provide leadership, tr...
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, ...
...Supports the day-to-day operations of the data management projects, providing in-house data entry support to projects and administrative support to CDMs, according to GCDMP guidelines, local regu...
...Research Associate/Grant Writer JD
Work from home, UK client, Full-timeResearch Associate/Grant Writer
This role is for a substantial, fast-growing and well respected UK tech company whohas hired us to exclusive...
...JOB DESCRIPTION
Brief Position Description:
Supports the day-to-day operations of the data management projects, providing in-house data entry support to projects and administrative support ...
About the Role
1. Act as Data Science SME/Lead for global project teams, with oversight for key outputs and deliverables. Provides technical and analytical expertise on assigned preclinical and clinical projects.
2. Attract, recruit, and develop ...
...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 ...
...Liaisonwithclientcompanies/monitoring staff asappropriate,ensuring effective studycommunication with internal and external stakeholders
f. Liaison with external service providers on Data Management projects as ap...
...management and regulatory compliance, data analytics, and business transformation.
Through a team of professionals ranging from actuaries to clinicians, technology specialists to plan administrators, we offer unp...
The Contract Associate will be responsible for the commercial relationship with sites involved in clinical trials including work from contract and amendment language, budget negotiation within the established timeline parameters. The Contract Associa...
