This is a full-time on-site role for a Clinical Research Coordinator at NovoBliss Research Private Limited
The Clinical Research Coordinator will be responsible for coordinating and managing clinical research studies, including activities such as informed consent, protocol adherence, data collection, and documentation
The role also involves working closely with the research team and ensuring compliance with ethical standards and regulatory requirements
Qualifications
Informed Consent and Protocol experience
Proficiency in clinical research practices
Previous experience with clinical trials
Strong organizational and time management skills
Excellent attention to detail
Good communication and interpersonal skills
Ability to work effectively in a team
Experience in data collection and documentation
Bachelors degree in a related field (eg, Life Sciences, Pharmacy, Nursing)
Knowledge of regulatory requirements for clinical research
