Trainee Clinical Research Cordinator
Aveda Bioreserch Center
Pune City, Maharashtra, India
Science / R&D / Research, Information Technology, Analyst
Company Description
Aveda Bioresearch Center specializes in delivering clinical trial and monitoring services that prioritize quality, compliance, and patient well-being. With expertise spanning study design, site management, regulatory adherence, and data monitoring, we are dedicated to ethical research and operational excellence. Our mission is to accelerate drug development while upholding the highest standards of integrity. Join us in driving medical innovation through effective and reliable clinical trial solutions.
Role Description
This is a full-time on-site role based in Pune City for a Trainee Clinical Research Coordinator. The role involves assisting in managing clinical trials, ensuring proper documentation of informed consent, and adhering to study protocols. Responsibilities include coordinating with study teams, monitoring patient enrollment, maintaining data accuracy, and adhering to regulatory requirements. The Coordinator will also assist in ensuring compliance with ethical standards and clinical trial guidelines.
Qualifications
Aveda Bioresearch Center specializes in delivering clinical trial and monitoring services that prioritize quality, compliance, and patient well-being. With expertise spanning study design, site management, regulatory adherence, and data monitoring, we are dedicated to ethical research and operational excellence. Our mission is to accelerate drug development while upholding the highest standards of integrity. Join us in driving medical innovation through effective and reliable clinical trial solutions.
Role Description
This is a full-time on-site role based in Pune City for a Trainee Clinical Research Coordinator. The role involves assisting in managing clinical trials, ensuring proper documentation of informed consent, and adhering to study protocols. Responsibilities include coordinating with study teams, monitoring patient enrollment, maintaining data accuracy, and adhering to regulatory requirements. The Coordinator will also assist in ensuring compliance with ethical standards and clinical trial guidelines.
Qualifications
- Strong understanding of Informed Consent processes and compliance
- Knowledge of study Protocols and Clinical Trials workflows
- Experience or academic background in Research and Clinical Research
- Attention to detail, organizational, and time management skills
- Effective communication and teamwork capabilities
- Bachelor's degree in Life Sciences, Pharmacy, or related field
- Familiarity with regulatory guidelines and ethical standards is a plus
About the company
Hospitals and Health Care
"At Aveda Bioresearch center, we provide comprehensive Clinical Trial and Monitoring Services to ensure high-quality, compliant, and patient-centric research. Our expertise includes study design, site management, regulatory compliance, data monitoring, and risk-based quality assurance. With a commitment to ethical research and operational excellence, we help accelerate drug development while maintaining the highest standards of integrity and efficiency. Partner with us to advance medical innovation through reliable and effective clinical trial solutions."