Accomplished Senior Study Coordinator at Clinical Research Malaysia (CRM), versatile clinical research professional knowledgeable about coordinating patient information, laboratory samples and compliance documents for diverse clinical trials. Highly organized and thorough with good planning and problem-solving abilities.
Organized and dependable candidate successful at managing multiple priorities with a positive attitude. Willingness to take on added responsibilities to meet team goals.
To seek and maintain full-time position that offers professional challenges utilizing interpersonal skills, excellent time management and problem-solving skills.
Overview
9
9
years of professional experience
Work History
Senior Study Coordinator
Clinical Research Malaysia (CRM)
06.2015 - Current
Streamlined communication between participants and research team, fostering effective collaboration and data collection.
Contributed to a positive work environment by fostering open communication, teamwork, and professional development opportunities for staff members.
Expedited study start-up timelines by efficiently coordinating site initiation visits, trainings, and equipment setup.
Assisted investigators with patient's visit as per protocol.
Improved data accuracy by implementing rigorous quality control measures during data collection and entry processes.
Ensured regulatory compliance by meticulously maintaining documentation for study activities.
Enhanced interdisciplinary collaboration among researchers by organizing regular team meetings and progress updates.
Optimized resource allocation for the research project, effectively managing budgets and personnel requirements.
Strengthened relationships with external partners such as clinical sites and vendors through effective communication channels and consistent follow-through on commitments.
Supported participant retention efforts by designing engaging materials that highlighted the benefits of continued involvement in the study.
Enhanced patient satisfaction by efficiently coordinating and managing study schedules.
Facilitated timely enrollment of participants through targeted recruitment strategies.
Promoted a culture of continuous improvement within the research team through constructive feedback on study processes and outcomes.
Collected data and followed research protocols, operations manuals, and case report form requirements.
Worked with principal investigator and sponsors to facilitate daily trial activities and comply with research protocols.
Monitored patient safety throughout clinical trials and reported any adverse events.
Collaborated with clinical staff and other healthcare professionals to support clinical trial data accuracy.
Maintained compliance with protocols covering patient care and clinical trial operations.
Managed patient recruitment, informed consent process and data entry to support trial objectives.
Developed and maintained accurate and up-to-date case report forms and source documents.
Followed informed consent processes and maintained records.
Screened patient records, databases, and physician referrals to identify prospective candidates for research studies.
Participated in initiation visits and investigator meetings, implementing trials following study timelines and budgets.
Maintained accurate and up-to-date case report forms and source documents for traceability.
Followed clinical research protocols and conducted study visits in compliance with ICH/GCP and FDA regulations.
Prepared and maintained regulatory documents for clinical trial submissions.
Gathered, processed, and shipped lab specimens.
Complied with research protocols by providing ongoing quality control audits.
Education
Bachelor of Science - Science Statistic
University Teknologi Mara (UiTM)
Kota Bharu, Kelantan, Malaysia
04.2001 -
Skills
Study design
Timeline
Senior Study Coordinator
Clinical Research Malaysia (CRM)
06.2015 - Current
Bachelor of Science - Science Statistic
University Teknologi Mara (UiTM)
04.2001 -
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