Clinical Research Coordinator (Data), HORG, Singapore

Overview National University Cancer Institute, Singapore (NCIS) is a national specialist center under National University Health System (NUHS). We're more than just a cancer center — we're a community of passionate professionals dedicated to advancing cancer care through innovation, research, and heart.
NCIS offers a unique and dynamic environment where your work truly makes a difference. From diagnosis to survivorship, we're with our patients every step of the way — and we're looking for like-minded medical professionals to join us.
If you're driven by purpose, inspired by challenge, and ready to grow in a world-class academic health system, your next chapter starts here. Let's change lives together!
Roles and Responsibilities Collecting clinical trial data by accessing patient's medical records to extract information on current and past medical history, medications, laboratory, imaging results. Provide clinical trial support such as data entry and transcription of information on source documents, paper case report forms (CRFs), or electronic CRFs. Manage clinical trials through review, computerization, cleaning and auditing of clinical data and in compliance with standard operating procedures. Validate clinical trial data to ensure consistency, integrity and accuracy. Reviewing patient records together with clinicians, radiologists, pharmacists and other members of the HORG team to address sponsor queries. Audits and spot checks to ensure compliance of drug prescriptions and processes with clinical trial requirements. Liaising with clinical CRCs to ensure compliance of informed consent forms with standards set by ethics committees and regulatory authorities Review case report forms for completeness and consistency Work in collaboration with study team to ensure trial preparedness
Requirements Possess degree in life Science, Nursing or related field Strong problem-solving and good communication skills (verbal and written) Ability to adapt to fast-moving situations, are required to manage interactions with investigators, study teams and management. Experience in data management will be an advantage. Good team player Organized and detail orientated. Good time management. Ability to multitask. Able to work both independently and in a team Computer Literate