Rinki Yadav

About Rinki Yadav

Clinical Trial Management: Proficient in overseeing all aspects of clinical trials, including study initiation, participant recruitment, data collection, and study closeout. Familiar with Good Clinical Practice (GCP) guidelines and regulatory requirements. Protocol Compliance: Demonstrated expertise in ensuring strict adherence to study protocols, maintaining accurate documentation, and coordinating with cross-functional teams to achieve study objectives. Project Coordination: Skilled in managing multiple research projects simultaneously, effectively prioritizing tasks, and meeting deadlines. Capable of maintaining accurate records, tracking study progress, and facilitating communication among study team members. Regulatory Compliance: Well-versed in FDA regulations, IRB processes, and ethical considerations in clinical research. Experienced in preparing and submitting regulatory documents, obtaining necessary approvals, and maintaining compliance throughout the study duration. Quality Assurance: Committed to maintaining high standards of data integrity, participant safety, and research ethics. Proficient in conducting monitoring visits, ensuring data accuracy and completeness, and implementing corrective actions as needed. Team Collaboration: Strong interpersonal skills, collaborating effectively with investigators, study coordinators, and other stakeholders. Capable of building rapport with study participants, providing support, and addressing any concerns. Data Management: Experienced in electronic data capture (EDC) systems, data entry, and data verification. Skilled in ensuring data accuracy, confidentiality, and quality control measures. Communication: Excellent written and verbal communication skills, including the ability to communicate complex scientific concepts to diverse audiences. Experienced in preparing study-related materials, including protocols, informed consent forms, and progress reports.

Experience

1. Clinical Research Coordinator

   Meril

   May 2022 — Present · Mumbai, IN

   Conduct Trial for the multispecialty sites.\\\\n Screened and recruited subjects based on eligibility criteria\\\\nfor project participation.\\\\n Conduct informs consent form after eligibility of subjects.\\\\n Arrange and Conduct follow-up visits of subjects based on\\\\ncriteria of project protocol.\\\\n Create source documents, maintain reports related subjects\\\\nand entered all data of subject on EDC2go, Crf Web.\\\\n Prepared the Site file logs, Update the SVT

Education

• Dr. A.P.J. Abdul Kalam Technical University

  Bachelor's degree, Pharmaceutical Sciences

  2010 — 2014

• PSIT Kanpur (Pranveer Singh Institute of Technology)

  M. Pharm, Medicinal and Pharmaceutical Chemistry

  2014 — 2016