Clinical Research professional

Experienced in conducting research, performing data collection and analysis, supporting laboratory activities, and contributing to project planning and execution, along with preparing reports, assisting with regulatory documentation, and collaborating with interdisciplinary teams to advance oncology research and ensure the successful, ethical execution of clinical trials.\n\nQualifications\nMaster’s degree in Pharmacy (MPharma) or Doctor of Pharmacy (Pharm D) from a recognized institution\nStrong understanding of clinical research processes, including ICH-GCP guidelines and regulatory requirements\nHands-on experience or training in site management, subject recruitment, and clinical trial coordination\nKnowledge of adverse event reporting, source document verification, and case report form (CRF) completion\nProficiency in data collection, analysis, and maintaining accurate study documentation\nFamiliarity with laboratory procedures and oncology research methodologies is an advantage\nAbility to prepare technical reports, regulatory documents, and study-related documentation\nStrong organizational, analytical, and problem-solving skills\nExcellent communication and interpersonal skills for effective collaboration with multidisciplinary teams\nProficiency in MS Office and clinical data management systems\nHigh attention to detail with a commitment to ethical standards and patient safety\nFamiliarity with oncology research and/or experience in clinical research is a plus