Website:
neuheitservices.com
Job details:
Company Description
We are hiring for our partners SMO. The team of highly skilled Clinical Research Coordinators (CRCs) supports investigators by managing non-medical study activities, adhering to Good Clinical Practice (GCP) standards, and maintaining ethical compliance.
Role Description
This is a full-time Clinical Research Coordinator role based in Pune District, on-site. The Clinical Research Coordinator will be responsible for tasks such as obtaining informed consent from study participants, coordinating with Principal Investigators, managing study protocols, and ensuring compliance with clinical trial regulations. The role also involves assisting in the execution, documentation, and monitoring of clinical research activities, maintaining accurate and complete data, and adhering to ethical standards and regulatory guidelines.
Qualifications
- Experience and knowledge in Informed Consent processes and Protocol development
- Strong background in Research and Clinical Research Experience
- Comprehensive understanding of Clinical Trials methodology and processes
- Strong organizational and communication skills
- Attention to detail and ability to handle multiple tasks effectively
- Ability to work collaboratively with cross-functional teams and investigators
- Familiarity with Good Clinical Practice (GCP) guidelines is required
- Bachelor's / Masters degree in life sciences, healthcare, or relevant field
- Prior experience in clinical trial coordination is an advantage
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