A. Negotiate study budgets with investigators and ensure that timely payments B. Responsible for training of site study team regarding the monitoring plan, recording & maintenance of essential documents and for start up activities & site initiation as per the guidance of Project Manager. C. Assist for the preparation and presentation at investigator meetingsD. Conduct of monitoring visits as per monitoring plan in order to check compliance with study management, protocol & other requirements at all assigned sites. E. Maintaining a working copy of Central Investigator File & ensuring consistency with the Site Investigator File in order to maintain a working record of all essential documents and reports. F. Perform source document verification as per monitoring plan and ensure that source documents & other trial records are accurate, complete, kept up-to-date & maintained according to applicable SOPs to avoid incomplete records.G. Ensure timely collection of documents like CRF, DCF etc from the site along with SAE reports H. Responsible for study updates & Coordination with Lab.I. Responsiblefor IP accountability and availability, tracking and management of all Clinical Trial related supplies shipped to the sites.J. Ensure proper escalation of site/project related issues to Project Manager/ Designee.K. Responsible for site-closeout & follow up activities.L. Attend staff meetings and training sessions.M. Assist with the audit of an investigational site or central files and liase with Quality Assurance personnel.N. To liaise with other departments within the organization for timely achievement of the project milestones. O. Identify and qualify potential investigators to ensure that the sites have adequate time and fulfill their obligation to the study. P. Responsible for identification & collection of necessary documents.Q. Prepare or submit or support other colleagues for Regulatory and EC submissions.

• Attend and facilitate Investigators’ Meeting.• Training of Investigators on Protocol and other applicable regulatory guidelines including local regulatory guidelines.• Perform Site visits (i.e. Site Selection Visit, Site Initiation Visits, Site monitoring visits and site close-out visits) in accordance with the protocol and other applicable regulatory guidelines including local regulatory guidelines• Send Follow up letters to sites and submit Visit Reports to the Clinical Team Leader/ Project Manager as required• Keep a close association with site (s) for: Patient Recruitment, Patient Follow Up, and protocol related activities• Ensure compliance of all study related requirements and its documents/data. • Coordinate and distribute Clinical Study Materials to study sites• Ensure calibration of all equipment to be used for the study prior to performance of study related activities by site team and re-calibration in timely manner as required during the trial conduct.• Ensure the traceability of equipment in the source data for its usage in the trial related activities and availability of list of equipment used during the trial. • Act as a communication Link between CRO team and the siteMaintain updated Site Files and collection of project related documents during the site visits and maintain Site Master file• CRF retrieval/ e-CRF review as per the project management plan and project manager instructions• Archival of study documents in a timely manner at sites or at third party archival facility as per prevailing SOPs and project management plan.• Any other responsibilities as assigned by the Management / HOD• Maintain accurate and timely sponsor/site correspondence and communication

1. Assist Project Manager with accurately updating and maintaining clinical systems that track site compliance and performance within project timelines.2. Assist the PM in the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures at Lambda. 3. Ensure the TMF/E-TMF and Site master files are updated all the times. .4. Responsible for timely disbursal of Investigator payments based on Invoices received from sites5. Assist with the tracking and management of Case Report Forms (CRFs), queries and clinical data flow.6. Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation.7. Updates various study trackers assigned by Project Manager.8. Maintenance of trial related documents and files within the facility.9. Liaising with other functional groups and providing updates to Project Manager.10. Any other responsibilities as assigned by the Management / HOD

1. Design and implement innovative methods of teaching.2. Teach both undergraduate students who are pursuing their own field of expertise.3. Prepare daily lessons and targets for the students.4. Mentor the students with their academic progress.5. Guide and mentor the research students in their projects.6. Assist or lend a helping hand to the superior professors in performing their duties and functions.7. Carry out the publishing of the university’s research works in journals and academic books.8. Develop professional logistics to help the students improve their performances.9. Support the functional activities of the department.10. Facilitating a learning environment that encourages the thirst for knowledge.