Clinical Research Coordinator (Contract)
at NATIONAL UNIVERSITY HOSPITAL SINGAPORE PTE LTD
Singapore, Southeast, Singapore -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 19 Oct, 2024 | USD 6300 Monthly | 20 Jul, 2024 | N/A | Life Science,Computer Literacy,Communication Skills | No | No |
Required Visa Status:
Citizen | GC |
US Citizen | Student Visa |
H1B | CPT |
OPT | H4 Spouse of H1B |
GC Green Card |
Employment Type:
Full Time | Part Time |
Permanent | Independent - 1099 |
Contract – W2 | C2H Independent |
C2H W2 | Contract – Corp 2 Corp |
Contract to Hire – Corp 2 Corp |
Description:
JOB SPECIFICATION/REQUIREMENTS
- Life science diploma/ degree or nursing degree is preferred. The relevant degree subject area is life science or biomedical science.
- Ability to work both independently and in a team.
- Good communication skills.
- Good patient interaction skills.
- Be flexible and self-motivated.
- Ability to write clearly
- Possess excellent organisational skills.
- Enjoy paying attention to detail.
- Computer literacy.
- Ability to work flexibly with occasional weekends and late nights.
Responsibilities:
JOB PURPOSE
- A clinical research coordinator will assist Principal Investigator or Co-investigators to monitor the administration and progress of a clinical trial.
DUTIES AND RESPONSIBILITIES
Primary Duties and Responsibilities
Clinical Trial
- Oversee overall clinical operations related to the conduct of the clinical trials.
- To adhere to compliance with Research Governance, Good Clinical Practice, Data Protection and Ethical Requirements.
- To ensure the study and study procedures are conducted in accordance with the study protocol
- To participate in patient recruitment.
- To ensure study entry criteria are fulfilled.
- To ensure informed consent procedure is followed.
- To coordinate patient visits for future tests and procedures.
- To schedule visit according to study protocol.
- To organize and participate in site initiation visit.
- To work in collaboration with study team to ensure trial preparedness.
- To monitor patients throughout the study to ensure study drugs are given according to protocol requirement.
- To arrange for clinical and laboratory investigations to be carried out according to protocol.
- Ensure results of investigations and X-ray films are collected.
- Maintains records of additional investigations for invoicing purposes.
- To collects and collates research data, ensuring its accuracy and completeness.
- Ensure timely and accurate transcription of information on source documents, paper case report forms (CRFs), or electronic CRFs.
- To label and ensure biological specimens are delivered in the correct conditions as specified in the trial protocol.
- To assist investigator(s) in adverse events / serious adverse events reporting.
- To maintain confidentiality on patient data.
- To work with pharmacy to maintain drug accountability logs.
- To raise payment request forms for billing to companies
- Creation and maintenance of all trial files, including the trial master file, and oversight of site files.
Secondary Duties and Responsibilities
Recruitment Plan
- To work with company in developing and implementing recruitment plan to ensure long-term recruitment target is met.
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Clinical Pharmacy
Graduate
Proficient
1
Singapore, Singapore