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Clinical Research Coordinator (Contract, STAR KIDS)

Salary undisclosed
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The Clinical Research Coordinator role is to coordinate, perform and assist in entering of patient data into a database. He/she would also have to manage and maintain effective data entry, organize database that allows future data mining and analysis across the 5-year programme. The CRC will also assist investigators in maintenance of Investigator Site Files, assist PI in safety reporting, submission to CIRB, any preparation for audit and inspection.

Job Description
  • Assist the investigators to recruit, screen, take consent and follow up participants of the study, in strict adherence to the study protocol and other applicable regulatory and ethical requirements.
  • Handle entry and validation of study data, extraction of relevant information from medical records, reporting of adverse events, maintenance of investigators files and other essential documentation.
  • Prepare and sort information before entering data into database and maintain data entry accuracy and quality levels to support team productivity and efficiency.
  • Resolve incomplete information and data discrepancies.
  • Coordinate scheduling and conduct of focus groups, interviews, as well as visits for stakeholders and study participants, as well as related finances (such as reimbursements) and logistics.Support in other functions such as general administration or coordination as required.
  • Respond to requests for information from authorised members.
  • Prepare relevant grant reports as needed and coordinate CIRB submission.
  • Maintain the highest standard of professional conduct and record keeping in accordance with policies and procedures.
  • Perform and assist with any other duties of a similar nature that are delegated by the Programme Leads.

Job Requirement
  • Degree in Life Sciences/Pharmacy/Nursing and any other relevant disciplines or Diploma in Life Sciences/Pharmaceutical Science/CT Mgmt with min 6 yrs CRC/relevant exp and Demonstrated competency
  • Prior clinical research experience will be advantageous.
  • Proficiency in Microsoft Office.
  • Good communication and interpersonal skills.
  • Highly motivated and able to work independently, as well as collaboratively in a diverse and interdisciplinary team.
  • Proficient in ensuring adherence to institutional guidelines, policies and regulatory requirements throughout project lifecycle.