Vishwambari Tamane

About the Candidate

Clinical Research Assistant Intern                                                                 March 2022- Present

Access Clinical Research, Montreal, Quebec, Canada

·        Researcher working on clinical trials in oncology

·        Prepare presentations for the clinical trials

·        Update and ensure the quality of presentations and documents according to recent information

·        Monitor and track clinical trends, patterns, and practices

·        Data capture and analysis of various methodologies, drugs, and procedures used in oncology

·        Review research study requirements and draft evaluation reports

Clinical Research Graduate                                                                      August 2021 to April 2022

International Clinical Research Academy, Montreal, Canada

·        Traced clinical trials, protocol synopsis, feasibility questionnaires, SOP checklists, information brochure (IB), informed consent design

·        Executed study start-up (SSU) activities like reviewing of informed consent form, information collection for protocol compliance

·        Integrated medical and periodic reports in addition to reviewing and submitting case report forms

·        Verified reporting on safety, adverse effects (AE), and serious side effects (SAE)

·        prepared support for close out visits of centers upon completion of study trials

Clinical/Research Assistant                                                                      July 2012- Feb 2019

Veda Holistic Healthcare, Hyderabad, India

·        Administered Mistletoe Therapy (Helixor) to cancer patients as an alternate therapy along with the conventional treatment

·        Recorded and reported outcomes of Mistletoe Therapy on patient immunity and tolerability of conventional drugs

·        Maintained records of drug supply, dispense, storage, and dosage

·        Supervised patient enrollment log, source documentation, and case report forms

·        Served as immediate point of contact for information and queries for patients and their families

·        Presented effects of Mistletoe (Helixor) on early-stage Breast cancer along with conventional treatment

·        Compiled research data to be used for multicenter research trials

·        Trained site staff on therapeutic areas, protocol requirements and prepared interview questions

·        Ensured strict compliance to study relevant standard operating procedures (SOPs)

·        Analyzed qualitative data stemming from various research projects

Certifications

Good Clinical Practice (GCP)- Canada CITI Program Certificate

Responsible Conduct of Research CITI Program Certificate

Tri-Council Policy Statement: Ethical Conduct for Research Involving Humans Certificate