We are looking for experienced Clinical Research Associates to join a growing Clinical Affairs team.
Key Responsibilities:
Clinical trial handling and site management
CRO coordination and monitoring activities
Ethics Committee submissions and regulatory documentation
Site initiation monitoring and close-out activities
Training site staff on protocols and GCP requirements
Subject safety and compliance management
Investigational Product accountability and reconciliation
Preparation of monitoring reports and study documentation
Ensuring compliance with ICH-GCP guidelines and SOPs
Requirements:
35 years of Clinical Research experience
Strong experience in Clinical Trial Handling
Hands-on exposure to CRO Management
Experience in Ethics Committee submissions
Good understanding of ICH-GCP and regulatory requirements
Interested candidates can share their updated resume.
Required Skills:
Healthcare HR expertise Labor law & compliance knowledge Strong stakeholder management Conflict resolution & negotiation Process orientation Leadership & team management Data-driven decision making
Required Education:
MBA- HR or relevant Experience in Hospital Industry.
Hiring: CRA / Senior CRA Location: NoidaWe are looking for experienced Clinical Research Associates to join a growing Clinical Affairs team.Key Responsibilities: Clinical trial handling and site management CRO coordination and monitoring activities Ethics Committee submissions and regulatory documen...
Hiring: CRA / Senior CRA
Location: Noida
We are looking for experienced Clinical Research Associates to join a growing Clinical Affairs team.
Key Responsibilities:
Clinical trial handling and site management
CRO coordination and monitoring activities
Ethics Committee submissions and regulatory documentation
Site initiation monitoring and close-out activities
Training site staff on protocols and GCP requirements
Subject safety and compliance management
Investigational Product accountability and reconciliation
Preparation of monitoring reports and study documentation
Ensuring compliance with ICH-GCP guidelines and SOPs
Requirements:
35 years of Clinical Research experience
Strong experience in Clinical Trial Handling
Hands-on exposure to CRO Management
Experience in Ethics Committee submissions
Good understanding of ICH-GCP and regulatory requirements
Interested candidates can share their updated resume.
Required Skills:
Healthcare HR expertise Labor law & compliance knowledge Strong stakeholder management Conflict resolution & negotiation Process orientation Leadership & team management Data-driven decision making
Required Education:
MBA- HR or relevant Experience in Hospital Industry.