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.
- Conducting informed consent procedures.
- Ensuring protocol adherence.
- Collecting and documenting data accurately.
- Working closely with the research team.
- Ensuring compliance with ethical standards and regulatory requirements.
Qualifications:
- Experience in informed consent and protocol adherence.
- 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.
- Bachelor’s degree in a related field (e.g., Life Sciences, Pharmacy, Nursing).
- Knowledge of regulatory requirements for clinical research.