Job Description

Job Title
Senior/Clinical Research Associate (3 year contract)



About SCRI
The Singapore Clinical Research Institute (SCRI) is the national coordinating body (NCB) for
clinical trials with a vision to establish Singapore as a regional thought leader in clinical
research. This is accomplished through the deployment of innovative technologies and
processes, and strategic coordination of ecosystem capabilities and infrastructure to achieve
synergies that will enhance the clinical research ecosystem aimed towards a healthier
community and better patient outcomes.

The Role: You will be responsible for planning, monitoring and coordinating of clinical trials within the
region. Your responsibility will include:

• Collaborate with Study Management Team to drive patient recruitment and successful

execution of clinical studies.

• Independently perform site qualification, site initiation, site routine monitoring, site

management and site close out visits ensuring GCP/ICH/protocol compliance.

• Work with site personnel and study team to prevent, mitigate and resolve issues.
• Document monitoring activities in monitoring reports, follow-up letters and other required

documentation as per SOPs and site monitoring plan.

• Review Informed Consent process documentation, conduct source document review and

source data verification of CRFs, DCFs, as stipulated.

• Ensure the reporting of high quality data and timely query resolution
• Ensure that the site is reporting safety events appropriately and in a timely manner.
• Process SAE reports and perform reconciliation.
• Organize, present at and participate in Investigator Meetings, other study trainings and

meetings as required

• Assist investigator in IRB/EC &RA submission.
• Manage trial financial payment including site payments.
• Coordinate with sites in preparation for study site audits and in providing responses to audit

findings as stipulated.

• Assist in the review of CRF design & CRF completion guidelines.
• Provide training for training events organized by SCRI Academy as required.
  

Requirements:

• Degree in Health Sciences/Nursing/Pharmacy/Clinical Research/related field.
• At least 3 years of experience in clinical trial
• For senior CRA, preferable with Phase I monitoring experience
• Those with clinical research monitoring experience in a Pharmaceutical Company or a

CRO will have added advantage

• Have some knowledge of clinical trial monitoring, drug development process, GCP,

regulatory requirements of regional countries, basic knowledge of project management
and medical terminology. Restricted, Non-Sensitive

• Have strong communication, time management and interpersonal skills.
• Ability to take initiative and work independently.
• Be proficient in English and have good writing skills.
• Be able to travel
• Be organized and have attention to detail
• Have a professional appearance and demeanor

Please send your application to career@cris.sg Please indicate in your email the following header: Application for Senior/Clinical Research
Associate (SCRI) Company Overview The Consortium for Clinical Research and Innovation Singapore (CRIS), a wholly owned
subsidiary of MOH Holdings, was established in 2020 with the goal of strengthening
synergies and promulgating strategies for national-level clinical research and translation
programmes under the stewardship of the Singapore Ministry of Health. The former
Singapore Clinical Research Institute Pte Ltd was repurposed to form CRIS which brings
together five entities as business units under a common management and governance
structure. These are the Singapore Clinical Research Institute (SCRI), the National Health
Innovation Centre (NHIC), the Advanced Cell Therapy and Research Institute Singapore
(ACTRIS), the Precision Health Research Singapore (PRECISE), and the Singapore
Translational Cancer Consortium (STCC). Additional Company Information Average Processing Time Industry
25 days Healthcare / Medical



Benefits & Others
Dental, Miscellaneous allowances, Medical, Regular hours, Mondays-Fridays Restricted, Non-Sensitive