Kalyani Phate-Charmore Email & Phone Number

Mississauga, On, Ca

Toronto, Ontario, Canada

Toronto, Ontario, Canada

Key Responsibilities:• Arrange and coordinate SIVs• Create and maintain patient tracker and source documents• Prepare protocol and consent form amendments for ethics submission• Safety report and SAE submissions to REB• Preparing for monitoring visits and audits and timely reconcile items noted on monitoring report• Ensure timely and accurate CRF completion and data entry• Communicate with study team, research ethics board and sponsor• Obtain timely tumor… Show more Key Responsibilities:• Arrange and coordinate SIVs• Create and maintain patient tracker and source documents• Prepare protocol and consent form amendments for ethics submission• Safety report and SAE submissions to REB• Preparing for monitoring visits and audits and timely reconcile items noted on monitoring report• Ensure timely and accurate CRF completion and data entry• Communicate with study team, research ethics board and sponsor• Obtain timely tumor measurements• Track protocol deviations• Data and Regulatory coordination of phase1, 2 and 3 oncology clinical trials Show less

Toronto, Ontario, Canada

Key Responsibilities:• Reconcile In and Out of inventory supplies and maintain the inventory tracker • Conduct administrative duties for the management team which includes data entry of medical records and processing CSRs• Coordinate and ensure timely availability of PPE supplies to the field staff• Organize and archive client medical records• Coordinate office activities, troubleshoot or escalate basic office administration issues.• Provides clients with… Show more Key Responsibilities:• Reconcile In and Out of inventory supplies and maintain the inventory tracker • Conduct administrative duties for the management team which includes data entry of medical records and processing CSRs• Coordinate and ensure timely availability of PPE supplies to the field staff• Organize and archive client medical records• Coordinate office activities, troubleshoot or escalate basic office administration issues.• Provides clients with accurate information and timely assistance to support a positive outcome through PROCURA scheduling system Show less

Pune Area, India

• Assisted the Principal Investigator in study start-up, which included completion of 1572, Financial Disclosure forms, QIU, submission of trial documents to REB and helped with closeout activities• Conducted telephonic screening of subjects and administrated telephonic questionnaires• Consented and recruited study participants as well as coordinated their follow up visits• Ensured accurate of transcription of data in source documents and electronic case report… Show more • Assisted the Principal Investigator in study start-up, which included completion of 1572, Financial Disclosure forms, QIU, submission of trial documents to REB and helped with closeout activities• Conducted telephonic screening of subjects and administrated telephonic questionnaires• Consented and recruited study participants as well as coordinated their follow up visits• Ensured accurate of transcription of data in source documents and electronic case report forms• Resolved the Electronic Data Capture queries in timely manner• Performed accountability ,inventory and storage of study drug(IP) • Reported Serious Adverse Events ,SUSARS and CIOMS to the Sponsor and REB • Prepared for sponsor monitoring visits as well as QA and QC audits• Maintained protocol specific Trial Master files, logs and trackers for screening and recruitment• Performed processing, labeling, storage and shipment of trial related biological samples Show less

Pune Area, India

Key responsibilities performed:• To conduct the clinical research study according to the study protocol, GCP, and the Lifepoint Research SOP• To recruit and screen patients for participation in clinical research studies• To obtain proper written informed consent from each study participant prior to participation in the study• To schedule study participant visits as per protocol• To perform delegated protocol specific activities completely and accurately• To obtain… Show more Key responsibilities performed:• To conduct the clinical research study according to the study protocol, GCP, and the Lifepoint Research SOP• To recruit and screen patients for participation in clinical research studies• To obtain proper written informed consent from each study participant prior to participation in the study• To schedule study participant visits as per protocol• To perform delegated protocol specific activities completely and accurately• To obtain vital signs as required per protocol (i.e. blood pressure, temperature, heart rate, waist measurement, weight & height)• To obtain all necessary documentation as required by the protocol (i.e. ECG, echocardiogram or pulmonary function test results)• To monitor and report all adverse experiences and abnormal results to the Investigator and Sponsor• To update and maintain subject screening and enrollment logs• To create source documents and any other research documents required for the successful conduct of a clinical research study• To meet with the Sponsor's representatives to discuss the conduct of the study and review study data Show less

Pune Area, India

Key responsibilities performed:• Assess each patient's level of function and identify problem areas;• Establish treatment goals based on assessment findings and then plan and initiate a treatment program that is continually monitored;• Document initial assessment findings and at regular intervals reassessments and progress notes in patient's medical records.• Treated patients with various musculoskeletal and neurological impairments

Pune Area, India

Bhandara Area, India

Bachelor Of Physiotherapy (Bpth), Physical Therapy/Therapist

Post Graduate Diploma In Clinical Research, Clinical Research