...Responsibilities:
1. Candidate must have experience as medical advisor in the medical affairs team of ESA (Erythropoietin stimulating agents)
2. Understand and keep up to date with the latest medical research in ...
...standard clinical trials for Herbal, Nutraceuticals, and Ayurvedic products.
Role Description
This is a full-time on-site role for a Medical Writer at NovoBliss Research. The Medical Writer will be responsible fo...
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, ...
Education and Experience Requirements/Qualifications:
Base Level:
• Bachelor’s degree or equivalent, preferably in Computer Science.
• Minimum of 8 to 17 years’ experience building EDC databases in support of clinical research.
• Technical ...
...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...
...Location: Delhi/Mumbai/Hyderabad
Business Unit: CMR (Clinical, Medical, Regulatory & Pharmacovigilance)
Are you passionate about what you are doing? Do you want to build excellence within processes in the ...
Company Description
Jaidev Pharma Placement is a pharmaceutical sales and human resources agency with over two decades of expertise. We focus on offering exceptional human resources services across India at highly competitive rates.
Role Des...
Welcome to my research project aimed at exploring the potential benefits of various meditation and visualization techniques.
What we’re doing:
This is one part research project, and one part practical application. We’v...
...1. Candidate must have experience as medical advisor in the medical affairs team of ESA (Erythropoietin stimulating agents)
2. Understand and keep up to date with the latest medical research in your field of expe...
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...