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
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