
Timeline
About me
Clinical Research | Clinical Trials | Grant Administration | Contract negotiation | Events Management
Education

School of the arts singapore
2013 -International baccalaureate diploma
Newcastle university
2014 - 2017Bachelor’s degree biological and biomedical sciences upper second-class honours (2:1) degree• Degree Classification: 2nd Class, First Division [2:1]• Scientific data and results from dissertation were presented at the British Society for InvestigativeDermatology Annual Meeting in Manchester (UK).
Experience

Apsaras arts premier performing arts company
Dec 2013 - Jun 2014Executive administrator-Handled fees, drafted sponsorship letters, promoted events (publicity) and assisted the founder and artistic director of the company with ad-hoc tasks.-Liaised with various highly reputable organizations including National Arts Council (Singapore) and Milapfest (UK) to coordinate major productions and workshops in Singapore such as Dance India Asia Pacific.
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Ministry of education, singapore (moe)
Jan 2014 - Aug 2014Relief allied educator
A*star - agency for science, technology and research
Nov 2017 - Jul 2018Research assistant• Competent in performing techniques such as Cell/tissue culture, DNA/RNA extractions from biopsies and blood, Polymerase chain reactions (PCR), Hematoxylin and eosin staining, PCR Purifications, Gel electrophoresis, Cryo-sectioning and Magbio HighPrep PCR.• Recognized by supervisors for meticulous attention to detail, as well as the ability to quickly learn new skills and adapt to evolving circumstances.• Designed experimental workflow independently and exhibit detailed documentation of protocols. Show less
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Ministry of health (singapore)
Aug 2018 - Sept 2019Executive• Assisted in pre-application and post award tracking process of Human Capital Awards, such as, Clinician Scientist awards, Transition awards and Singapore Translational Research awards through the Integrated Grant Management System [IGMS].• Generated proposal reports, review the completeness of grant applications, sourced for local and international reviewers and provided overall administrative support at panel meetings.• Demonstrated the ability to quickly learn the workflow and had the opportunity to guide new temporary staffs within the department.• Extracted and collated data relating to research Key Performance Indicators (KPIs) with accuracy within stipulated timeline.• Responsible for confidential and time sensitive materials. Show less

Tan tock seng hospital
May 2020 - Mar 2021• Managed phase I-III clinical trials in various therapeutic areas such as, Cardiology, Haematology and Renal Medicine.• Screen, obtain informed consent, enrol, educate patients during recruitment period and assess patients' ability and willingness to follow-up and complete study procedures and visits.• Promptly communicate with Domain Specific Review Board (DSRB) regarding study-related ethics applications, amendments and study status reports.• Evaluate and interpret collated clinical data in conjunction with principal investigator(s); prepare written reports and analyse trends. Show less
Clinical Research Coordinator
Oct 2020 - Mar 2021Executive
May 2020 - Sept 2020

Parkway cancer centre
Oct 2021 - nowClinical research coordinator• Oversee the entire oncology clinical trial management to ensure seamless operations of the trials in strict accordance with Standard Operating Procedures (SOPs), study protocols, Good Clinical Practice (GCP) and all regulatory and ethical requirements.• Demonstrate excellent interpersonal skills to work effectively with internal and external stakeholders of the clinical research industry, patients, and a diverse study team.• Generate datasets for the purpose of outcomes reporting for the National Disease Registries Office (NRDO), Marketing and Finance department and possess the ability to understand medical terminologies to code these information.• Coordinate Tumour Board Meetings (Webinars), a multi-disciplinary discussion platform where rare or challenging oncology cases are presented by medical professionals on a monthly basis.• Responsible for all data collection, source documentation and developing/completing study-specific case report forms.• Manage all aspects of event logistics to ensure events and activities meet agreed quality, cost and timescale parameters.• Initiate clinical review and clinical practice improvement efforts to create and maintain high- performing and efficient team.• Support trial administrative matters such as budget projection, grant applications, Parkway Independent Ethics Committee (PIEC) applications and submissions and, coordinate study team meetings. Show less
Licenses & Certifications

Lean six sigma green belt
Lean methods groupMay 2023
Languages
- enEnglish
- taTamil
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