Clinical Research Intern

3 days ago

Singapore MIRXES LAB PTE. LTD. Full time

Roles & Responsibilities Job Summary A motivated Clinical Research Intern to join our team and gain valuable hands-on experience in the field of clinical research. This internship offers an exciting opportunity to contribute to the coordination and execution of clinical studies under the guidance of the clinical operations team. We welcome candidates who are passionate about healthcare and eager to learn in a dynamic environment. Roles & Responsibilities Site Management/Coordination: · Prepare and maintain study documentation including regulatory documents. · Perform study documentation audit for Clinical Research Organisations. · Monitor subject recruitment, enrolment, and retention at study sites. · Support shipment and tracking of consumables. · Address issues related to study conduct and data collection. · Coordinate and closely follow up with study sites for study related activities/documents/issues. · Communicate study progress and issues to the clinical operations team. · Collaborate and establish regular line of communication with both internal and external stakeholders. · Prepare meeting minutes · Review and reconcile financial documentation. Data Management: · Work with data manager in the efforts to oversee the sites’ compliance in data entry ensuring accuracy and completeness of study data. · Learn new electronic data capture system and build/ maintain data capturing system · Review and clean clinical study data to review for any inconsistencies. · Participate in data management activities, such as data query resolution, database lock, and generation of study-specific reports. Regulatory and Ethical board Compliance: · Gain a strong understanding of local/overseas regulatory requirements. · Review ethic board documents to assess accuracy. Desired Skills and Competencies · Currently undergoing clinical/life-science-related (biotech, pharmaceutical, nursing etc) degree/diploma. Relevant qualification in allied professions may also be considered. · Inquisitive and a self-starter · Reflects on day-to-day work and eager to fill in the gaps in knowledge. · Has an eye for detail, meticulous and works well independently. · Strong organizational, time management, interpersonal and problem-solving skills. · Effective written and verbal communication skills · Proficient in Microsoft Office Suite (Word, Excel, PowerPoint, Outlook) · Ability to learn new systems. Benefits · Hands-on experience in clinical research setting within a Sponsor. · Learning of clinical research regulatory framework, ICH-GCP guidelines and overall study conduct. · Exposure to various aspects of study coordination · Mentorship/guidance from clinical operations team · Opportunity to contribute to meaningful medical research and advancements in healthcare Tell employers what skills you have Microsoft OfficeClinical ResearchCROHealthcareData ManagementConsumablesClinical DevelopmentClinical OperationsClinical TrialsMedical AffairsProtocolBiotechnologyMedical ResearchResearch SkillsTime ManagementGCPRegulatory RequirementsAbility To LearnClinical Monitoring

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