Mirxes – Clinical Research Intern

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 pursuing a clinical or life science–related degree/diploma (e.g., biotechnology, pharmaceutical science, nursing). Relevant qualifications in allied health or related disciplines may also be considered.
• Inquisitive, proactive, and a self-starter.
• Reflects on day-to-day work and is eager to identify and close knowledge gaps.
• Detail oriented, meticulous, and able to work 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), with advanced Excel skills preferred (e.g., formulas, pivot tables, data cleaning, basic automation).
• Basic coding knowledge, preferably in Python or R, for simple data manipulation or analytics tasks.
• Ability to learn new databases and digital systems quickly, with strong technical adaptability.
• Comfortable learning and applying new tools or systems as part of daily workflow.

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