Clinical Research Coordinator

8 hours ago

Chennai Tamil Nadu, India Promed Hospital Full time

**Protocol Development & compliance**

Develop and adhere to comprehensive clinical trial protocols in collaboration with the Principal Investigator

**Participant Recruitment and Retention**

Implement effective strategies to recruit and retain study participants

**Data collection & management**

Oversee accurate and timely data collection entry and management

**Reguatory compliance and documentation**

Ensure all trial activities comply with regulatory guidelines and maintain thorough documentation

**Budget Management**

Manage the clinical trial budget effectively, ensuring cost efficiency.

**Team Coordination and Training**

Co-ordinate with cross-functional teams and provide necessary training to staff involved in the trial

**Patient safety monitoring**

Monitor participant safety and manage adverse events promptly

**Quality Assurance**

Implement quality control measures to ensure trial integrity

**Stakeholder Communication**

**Maintain effective communication with stakeholders, including sponsors, regulatory bodies and the PI (Principal investigators)**

**Continuous Improvement & Innovation**

Identify opportunities for process improvements

**Job Types**: Full-time, Permanent

**Benefits**:

- Provident Fund

Schedule:

- Fixed shift

Work Location: In person

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