6 Babe Studies Jobs

Role & responsibilities Clinical Research Physician-CPMA Monitor and manage adverse events Maintain and manage medical confidential reports Ensure compliance to protocol and SOPs Adverse tracking and follow-up of subjects Coordinate with screening and volunteer recruitment group on updates regarding volunteers adverse events and follow-up Handle safety related issues prior to and during the clinical phase of the study. Coordinate and conduct staff vaccination program and other related activities Others: Support clinical trial group Help for corporate check-up Write and review related SOPs Help maintain and update all the systems and SOPs in the department Train the staff on all SOPs related ...

Role & responsibilities Preferred candidate profile q Act as a Study Physician/Co-investigator q Prepare and review protocols for clinical studies q Co-ordinate activities related to IEC q Communicate IEC related issues to all concerned q Ensure compliance to protocol, SOPs and Regulatory requirements q Monitor and co-ordinate for volunteer recruitment and screening procedures q Handle medical confidential reports and case management. q Coordinate with Project Coordinators for all project related matters q Monitor and manage adverse events q Coordinate with panel of consultants to seek medical opinion as and when required q Ensure timely response to QA findings q Interact with sponsors on me...

Role & responsibilities Preferred candidate profile q Act as a Study Physician/Co-investigator q Prepare and review protocols for clinical studies q Co-ordinate activities related to IEC q Communicate IEC related issues to all concerned q Ensure compliance to protocol, SOPs and Regulatory requirements q Monitor and co-ordinate for volunteer recruitment and screening procedures q Handle medical confidential reports and case management. q Coordinate with Project Coordinators for all project related matters q Monitor and manage adverse events q Coordinate with panel of consultants to seek medical opinion as and when required q Ensure timely response to QA findings q Interact with sponsors on me...

Role & responsibilities: Responsible for creating, coordinating and maintaining the Master Study Schedule for all Cliantha sites. Working with all Head of Departments (HODs) of Cliantha Research on a regular basis to ensure the relevant project milestones are discussed and needs of Sponsor and functional areas are not compromised. Create, plan and monitor all project activities in PM database ensuring accuracy at all times. Responsible for identifying interdependencies for all projects and facilitate communication among functional areas where required. Understands time-sensitive nature of critical path project activities and notifies the relevant teams, and/or management of related issues. W...

PROJECT RELATED ACTIVITIES: Responsible for creating, coordinating and maintaining the Master Study Schedule for all Cliantha sites. Working with all Head of Departments (HODs) of Cliantha Research on a regular basis to ensure the relevant project milestones are discussed and needs of Sponsor and functional areas are not compromised. Create, plan and monitor all project activities in PM database ensuring accuracy at all times. Responsible for identifying interdependencies for all projects and facilitate communication among functional areas where required. Understands time-sensitive nature of critical path project activities and notifies the relevant teams, and/or management of related issues...

Role & responsibilities: Responsible for creating, coordinating and maintaining the Master Study Schedule for all Cliantha sites. Working with all Head of Departments (HODs) of Cliantha Research on a regular basis to ensure the relevant project milestones are discussed and needs of Sponsor and functional areas are not compromised. Create, plan and monitor all project activities in PM database ensuring accuracy at all times. Responsible for identifying interdependencies for all projects and facilitate communication among functional areas where required. Understands time-sensitive nature of critical path project activities and notifies the relevant teams, and/or management of related issues. W...