Mital Kansara
Clinical Research Coordinator @Cliantha Research Limited
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WORK HISTORY
Clinical Research Coordinator @Cliantha Research Limited
CA
Coordinating multiple clinical trials, including BE and Phase 1-4 studies. Expertise in overseeing patient recruitment, conducting study visits, and ensuring adherence to protocols, regulatory requirements, and GCP guidelines. Skilled in collaborating with Principal Investigators, sponsors, and cross-functional teams to ensure smooth study execution and timely completion. Proficient in managing investigational products, processing biological samples, and maintaining accurate documentation. Adept at preparing regulatory documents, participating in monitoring visits and audits, and utilizing EDC systems for data management. Committed to maintaining the highest standards of quality and compliance in clinical research.
EDUCATION
SARDAR PATEL COLLEGE OF PHARMACY COLLEGE, BAKROL 244
M.Pharm, Pharmacology
Imperial Institute of Clinical Research, Ahmadabad.
Advanced Post graduate Diploma in Clinical Research, Research
Conestoga College
Postgraduate Degree, Pharmacy Administration and Pharmacy Policy and Regulatory Affairs
Conestoga College
Postgraduate Degree, Health/Health Care Administration/Management
Dharamsinh Desai University Nadiad Gujarat in April 2014
Bachelor's Degree, Pharmacy
SKILLS
ABOUT MITAL KANSARA
With over 6 years of experience in the clinical research industry, I am a healthcare professional passionate about advancing medical science through rigorous clinical trial management. My academic background includes a master’s in pharmacy (pharmacology) and a specialization in regulatory affairs & project management from Conestoga College, Canada. My interests lie in clinical operations, regulatory compliance, and project leadership, where I have consistently excelled and been recognized for my academic and professional achievements.Throughout my career, I have managed and coordinated over 30 clinical trials spanning Phases 1–4, including BE studies, across therapeutic areas such as ophthalmology, cardiology, oncology, dermatology, pediatrics, and medical devices. My roles at Cliantha Research (Canada), CBCC Global Research, Meril Life Sciences, and Lambda Therapeutic Research (India) have honed my expertise in patient recruitment, protocol adherence, regulatory documentation, and stakeholder management. I am adept at utilizing electronic data capture (EDC) systems, ensuring GCP compliance, and leading cross-functional teams to deliver studies on time and within scope. My technical skills match my ability to mentor junior associates and foster collaboration among investigators, sponsors, and regulatory bodies.I am committed to data integrity, patient safety, and continuous learning. My work has contributed to the successful completion of high-impact studies, regulatory submissions, and the professional growth of my teams. I am eager to leverage my experience in a dynamic, innovative healthcare environment to drive clinical excellence and contribute to global medical advancements.If you are interested in collaborating or discussing opportunities in clinical research, please feel free to connect with me. Email: m••••••••@outlook.com LinkedIn:
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