As a Clinical Research Associate at Omega Healthcare, your main responsibility will be managing clinical trials and ensuring compliance with protocols and industry regulations. This position requires a focus on quality assurance, data integrity, and patient safety.
Key Responsibilities
1. Project & Operations Management
- Manage all aspects of clinical trials from start to finish.
- Prepare and maintain trial-related documentation.
- Ensure data completeness and submit findings to relevant stakeholders.
2. Quality Assurance
- Ensure trials comply with ICH-GCP guidelines.
- Improve the consistency of electronic data capturing (EDC) systems.
3. Protocol Monitoring
- Verify that investigators adhere to trial protocols and Good Clinical Practice (GCP) procedures.
- Communicate any observations or concerns to the sponsors for timely resolution.
4. Security Responsibilities
- Ensure the confidentiality of trial data.
- Follow data security protocols and regulations to maintain patient privacy.
Requirements
- Education: Bachelor’s or Master’s Degree.
- Experience: 1+ year in Clinical Trials Management, or 6 months with certification.
- Skills:
- Knowledge of oncology-specific terminology (preferred).
- Strong experience with Electronic Data Capture systems (EDCs) like Medidata RAVE, Oracle, Inform (strongly preferred).
- Experience with industrial protocols and monitoring visits (strongly preferred).
- Proficiency with computers and strong multitasking abilities.
- Excellent communication skills.
Job Location: Mumbai
Share your CV: Krushikant Pawar
📞 7892374090 | 📧 krushikantpawar@gmail.com
