- Coordinate and manage clinical trials from initiation to completion.
- Ensure compliance with all regulatory and ethical guidelines.
- Prepare and maintain essential trial documentation, including study protocols, consent forms, and case report forms.
- Monitor trial progress and address any issues or deviations.
- Communicate effectively with investigators, sponsors, and other stakeholders.
- Assist with data collection, entry, and analysis.
- Maintain accurate and organized records of all trial activities.
Qualifications:
- Bachelor’s degree in a scientific, medical, or health-related field.
- Previous experience in clinical research or a related field is preferred.
- Strong organizational skills and attention to detail.
- Excellent communication and interpersonal skills.
- Ability to manage multiple tasks and work independently as well as part of a team.
- Proficiency in Microsoft Office Suite.
Why Join Catalyst Clinical Services Pvt Ltd:
- Be part of a dynamic and innovative team dedicated to advancing clinical research.
- Opportunities for professional growth and development.
- Contribute to research that makes a real impact on patient health and wellbeing.
How to Apply:
Interested candidates are invited to send their CV to Pulkit at pulkit@catalystclinicalservices.com.
