Nisha Kapil Email & Phone Number

Toronto, Ontario, Canada

• Responsible for leading the Baby Constraint Induced Movement Therapy (CIMT) project that offers early intervention at rehabilitation centers across Ontario to infants with or at risk of hemiplegic CP.- Create proposals, budgets and data collection outcomes.- Facilitate training sessions to nurses and physicians. - Led monthly community of practice meetings with physicians, occupational therapists and research faculty. • Recruit participants, obtain informed consent, screen and… Show more • Responsible for leading the Baby Constraint Induced Movement Therapy (CIMT) project that offers early intervention at rehabilitation centers across Ontario to infants with or at risk of hemiplegic CP.- Create proposals, budgets and data collection outcomes.- Facilitate training sessions to nurses and physicians. - Led monthly community of practice meetings with physicians, occupational therapists and research faculty. • Recruit participants, obtain informed consent, screen and assess participant eligibility for an investigator-initiated, multi-site, Health Canada regulated clinical trial.• Prepare clinical trial applications/amendments for submission to the REB and Health Canada.• Development of study specific source documentation such as case report forms and maintain study logs and records of study related visits.• Conduct assessments (questionnaires and tests) and review medical charts as required by study protocol. • Facilitate site initiation and monitoring visits from Applied Health Research Centre.• Score and enter study data into REDCap including data checks and data verification.• Advanced knowledge using reference manager programs (EndNote), and intermediate knowledge of statistical analysis software (SPSS).• Monitor and report adverse events and protocol deviations to principal investigator.• Prepare reports, presentations as well as manuscripts for publication.• Ensure research is conducted in compliance with the Bloorview Research Ethics Board (REB), Tri-Council Policy Statement (TCPS-2), and ICH-GCP principles. Show less

Toronto, Ontario, Canada

Toronto

-Conducted and documented the clinical tasks required in the management of trials. -Ensured subject safety and compliance with study Protocol, SOPs, and Clinic Rules and Regulations.-Performed all relevant clinical and non-clinical functions during study conduct including, but not limited to, venipuncture, intravenous catheter insertion, vital signs, ECG’s, managing medical emergencies and recording and monitoring adverse events.-Monitored subjects and ensured that safety… Show more -Conducted and documented the clinical tasks required in the management of trials. -Ensured subject safety and compliance with study Protocol, SOPs, and Clinic Rules and Regulations.-Performed all relevant clinical and non-clinical functions during study conduct including, but not limited to, venipuncture, intravenous catheter insertion, vital signs, ECG’s, managing medical emergencies and recording and monitoring adverse events.-Monitored subjects and ensured that safety requirements or actions were implemented as necessary, including the ability to implement Advanced Medical Directives.-Conducted medical interviews and general psychometric testing, such as the Diagnostic and Statistical Manual of Mental Disorders (DSM–5) questionnaires. -Ensured that documentation was compliant with SOPs and Good Documentation Practices and that subject’s records were complete and accurate.-Provided instruction and support while working with multidisciplinary team members.-Performed verification of safety and screening-related equipment.-Obtained written and verbal informed consent.-Screened participants and determined eligibility of potential study subjects. -Reviewed source documentation such as screening sources, protocol and study specific procedures. Show less

Rochester, Minnesota Area

- Conducted multiple clinical studies examining the mechanisms of glucose regulation and insulin resistance in people with pre-diabetes, obesity and type 2 diabetes. - Responsible for managing various aspects of the research projects (recruited, consented and screened participants by conducting medical interviews and performing physical examinations).- Assisted with the set up and operated experimental protocol by infusing radioactive and nonradioactive isotope and hormones, inserted… Show more - Conducted multiple clinical studies examining the mechanisms of glucose regulation and insulin resistance in people with pre-diabetes, obesity and type 2 diabetes. - Responsible for managing various aspects of the research projects (recruited, consented and screened participants by conducting medical interviews and performing physical examinations).- Assisted with the set up and operated experimental protocol by infusing radioactive and nonradioactive isotope and hormones, inserted continuous glucose monitors, and performed oral glucose tolerance tests. - Compiled, analyzed and interpreted data, and wrote manuscripts for publication. Show less

Mississauga, Canada

Compiled and analyzed data from questionnaires, and presented findings to physicians to aid in the implementation of the “Be Healthy Live Well” and “Your Health Matters” cancer screening and prevention campaigns.

Brampton, Canada

Actively engaged in discussing colorectal cancer screening with patients; compiled and analyzed data, and presented findings to physicians in support of study aimed at determining whether taking proactive measures (calling patients in combination with readily available FOBT kits) in a family practice setting would increase rates of colorectal screening.

Doctor Of Medicine - Md, 3.9 Gpa

Bachelor Of Science - Bs, Major In Human Biology, Minor In Psychology