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Clinical Trials Coordinator (Pharma MNC/ Healthcare/ Restructured Setting)


Job Description

  • The Clinical Research Coordinator (CRC) will perform independently execute, manage, and coordinate research protocols, as directed by the Clinical Research Supervisor and/or Principal Investigator (PI); may coordinate the data collection and operations of several concurrent clinical research studies under the guidelines of research protocols and regulating agency policies. 
  • The CRC's duties may include, but will not be limited to supporting the management and coordinating the tasks of multiple clinical research studies
  • Act as intermediary between services and departments while overseeing data and specimen management
  • Manage and report on study results
  • Create, clean, update, and manage databases and comprehensive datasets and reports
  • Coordinate staff work schedules, assist with training of assistant crcs, and assist clinical research supervisor and/or pi with oversight of other research staff
  • Manage investigator’s protocols in the committee on human research system, as well as renewals and modifications of protocol applications and the implementation of new studies
  • Participate in the review and writing of protocols to ensure institutional review board approval within compliance
  • Help assure compliance with all relevant regulatory agencies; oversee study data integrity; implement and maintain periodic quality control procedures; interface with departments to obtain approval prior to study initiation
  • Maintain all regulatory documents
  • Report study progress to investigators
  • Participate in any internal and external audits or reviews of study protocols. 
  • This position is responsible for research coordination, training and direct supervision of research personnel, and project management at an independent level. 




  • Min Diploma/ Degree in Pharmaceutical Science/ Life Sciences or related field
  • Min of 2-3 years of working experience
  • Candidates with no experience are welcome to apply
  • Excellent communication skills is a must.
  • Preferably knowledge of ICH-GCP and relevant regulations (for experienced clinical research personnel only)
  • Meticulous and able to handle numbers is a must
  • Proficient in more than one language
  • Proficient in Microsoft Office


If you are interested in any of the positions, do kindly drop your most updated resume to (Attn: Clinical Research Coordinator - Leon)

Thank You. 


Leon Leong De Cong

Recruit Express Pte Ltd (Healthcare & Lifesciences Division)
EA License: 99C4599


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Central, North, East, West

Employment Type

Contract / Temp


S$2,601 - S$4,000 / mth
S$4,001 - S$6,000 / mth
S$6,001 to S$10,000 / mth

If you meet the requirements of this role, please email a detailed resume in Word document to Leon Leong De Cong.
CEI Registration No.: R1551708
*All information will be treated with strictest confidence. We regret that only short-listed applicants will be notified.