• Delegate tasks to the research department employees.• Supervise the screening of the patient’s eligibility according to Protocol specific Inclusion and Exclusion criteria and documenting the same.• Supervise the inform consent process. • Conduct budgeting and contract negotiation.• Conduct Site initiations. • Supervise research subject visits including history, physical exam and medicine refill. • Providing education on chronic diseases to the patients while emphasizing compliance with medication and lifestyle changes to achieve better health.• Enter necessary data in EMR. Send new prescribed medicine and refills of necessary drugs to the pharmacy• Supervise the maintenance of regulatory binders with new and updated site-related documents and review them for consistency with other documents and compliance with regulatory requirements, ICH guidelines, product SOPs and sponsor requirements.• Supervise the maintenance of Study time-lines and retain all study data in accordance with the protocol.• Assures timely completion of Case Report Forms as per protocol.• Conduct the monitoring visits and resolve active queries• Serve as a primary liaison between Primary investigator, Research subjects, and sponsors.• Effective communication with laboratories or investigators regarding laboratory findings.• Reports Serious adverse event (SAE) and assist in the completion of SAE reports.

• Delegate tasks to the research department employees.• Review patient charts for screening processes. Enter necessary data in EMR. Send new prescribed medicine and refills of necessary drugs to the pharmacy.• Serve as a primary liaison between Primary investigator, Research subjects and sponsors.• Conduct research subject visits including history, physical exam and medicine refill.• Providing education on chronic diseases to the patients while emphasizing on compliance to medication and life style changes to achieve better health.• Effective communication with laboratories or investigators regarding laboratory findings.• Look over screening of the patient’s eligibility according to Protocol specific Inclusion and Exclusion criteria and documenting the same.• Supervise the inform consent process. • Conduct budgeting and contract negotiation.• Conduct Site initiations. Collect documents required to initiate the study and submit to sponsors (e.g FDA forms 1572, Financial disclosure) • Responsible for maintaining adequate inventory of study supplies.• Maintains regulatory binders with new and updated site related documents and review them for consistency with other documents and compliance with regulatory requirements, ICH guidelines, product SOPs and sponsor requirements.• Maintains Study time-lines and retain all study data in accordance with protocol.• Complete the source information and assures timely completion of Case Report Forms as per protocol.• Conduct the monitoring visits and resolve active queries• Reports Serious adverse event (SAE) and assist in completion of SAE reports.• Monitor study activities and implement according to protocol ,regulatory guidelines and institutional policies

Conduct Site initiations. Collect documents required to initiate the study and submit to sponsors (e.g FDA forms 1572, Financial disclosure) Participate in the informed consent process including explaining the research subjects, answering any question related to study,obtaining appropriate signatures where required and ensuring amended consent forms are implemented appropriately.Screen the patient’s eligibility according to Protocol specific Inclusion and Exclusion criteria and documenting the same.Inform research subjects about study aspects, outcomes to be expected ,information about using the devices if present in the study and emphasizing the need for their compliance.Serve as a primary liaison between Primary investigator, Research subjects and sponsors.Conduct research subject visits .Effective communication with laboratories or investigators regarding laboratory findings.Responsible for maintaining adequate inventory of study supplies.Maintains regulatory binders with new and updated site related documents and review them for consistency with other documents and compliance with regulatory requirements, ICH guidelines, product SOPs and sponsor requirements.Maintains Study timelines and retain all study data in accordance with protocol.Complete the source information and assures timely completion of Case Report Forms as per protocol.Conduct the monitoring visits and resolve active querriesReports Serious adverse event (SAE) and assist in completion of SAE reports.Monitor study activities and implement according to protocol ,regulatory guidelines and institutional policies

• Inform research subjects about study aspects, outcomes to be expected ,information about using the devices if present in the study and emphasizing the need for their compliance.• Serve as a primary liaison between Primary investigator, Research subjects and sponsors.• Conduct research subject visits including history physical exam and medicine reconciliation. • Providing education on chronic diseases and emphasizing on compliance to medication and life style changes to achieve better health.• Effective communication with laboratories or investigators regarding laboratory findings.• Conduct Site initiations. Collect documents required to initiate the study and submit to sponsors (e.g FDA forms 1572, Financial disclosure) • Participate in the informed consent process including explaining the research subjects, answering any question related to study,obtaining appropriate signatures where required and ensuring amended consent forms are implemented appropriately.• Maintains regulatory binders with new and updated site related documents and review them for consistency with other documents and compliance with regulatory requirements, ICH guidelines, product SOPs and sponsor requirements.• Maintains Study timelines and retain all study data in accordance with protocol.• Monitor study activities and implement according to protocol ,regulatory guidelines and institutional policies

• Review patient charts for missing diagnosis. • Add appropriate diagnosis for the patients..• Review procedure notes and add notes to corresponding visits if necessary.• Monitor future patient visits giving the physician heads up on necessary repeat testing or procedures.• Scheduling patients that are due for follow up. • Reconciling medicine and educating patients on importance of their compliance.• Providing education on chronic diseases and emphasizing on compliance to medication and life style changes to achieve better health.

Perform duties in Chest ICU and HDUHandle exacerbations, pulmonary embolism and other medical emergencies occurring during patient’s stay.Contribute to teaching and training doctors and other healthcare professionals. Contribute to discussions and decisions about improving the quality of services and outcomes.Manage patients in wards.Manage patients related to pulmonology in emergency department.Assess and advice the patients in opd.Directly responsible for patients to assess, treat, stabilize, admit, transfer to monitoring setup as required.Effective participation in all post graduate educational and quality improvement activities.Perform life saving procedures.Perform Chest tube intubations.Actively involved in counseling of the patients.Manage discipline of the department by organizing duties of the residents, house officers, students and elective students.Resolve active issues of the Residents and encourage them to improve and excel.Act as a positive role model.

Handled all kind of emergencies.Performed life saving procedures.Referring the patient to another practitioner, when indicated. Keep clear, accurate, medical records which report the relevant clinical findings, the decisions made, and any drugs or treatment givenDemonstrate effective team working and leadership.Effective counselling of patients and their attendants.Acting as a bridge of effective communication when multiple specialities involved in management of a single patient.Involved actively in improving the quality of care for the patients.

House Surgeon & Physician:SURGICAL WARD 3 SEP 06 TO FEB 07Responsible for the diagnosis, treatment, and referrals for the assigned patients.Attended ward daily and emergency once a week.Assisted in elective surgeries.Performed minor incision treatments.Assisted in basic medical and life saving proceduresPromote a working environment free from unfair discrimination, bullying and harassment, bearing in mind that colleagues and patients come from diverse backgrounds.Handled paperwork.MEDICAL WARD 6 MAR 07 TO MAY 07Assisted in basic medical and life saving procedures.Attended ICU on assigned days.Handled endocrine emergencies.Responsible for the diagnosis, treatment, and referrals for the assigned patients.Engage with colleagues to maintain and improve the safety and quality of patient care.PSYCHIATRY WARD JUL 07 TO OCT 07Handled patients diagnosis and treatment under supervision.Assisted in ECT (Electro Chemical Treatment).Raise and act on concerns about patient safety.Use resources efficiently for the benefit of patients and the public.

Handled the diagnosis, treatment, and referrals for patients.Handled respiratory and hemodynamic emergencies.Performed life-saving procedures.Treat patients as individuals and respect their dignity.Protect and promote the health of patients and the publicHandled the paperwork.