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*CLINICAL* Research Assistant (Lab, Coordinator, Analysis, Data collection, Permanent) at Recruit Express Pte Ltd

*CLINICAL* Research Assistant (Lab, Coordinator, Analysis, Data collection, Permanent)

Recruit Express Pte Ltd Central Area Permanent
2,800 SGD - 4,000 SGD/Month


·         Researches and collects data through site or home visit intakes; library research; structured interviews; or through other means for designated research assignments.

·         Records and compiles information related to research data.

·         Codes data accordingly to research specifications.

·         Uses a computer terminal to input and retrieve data and to generate reports.

·         Processes and summarizes data using scientific or statistical techniques

·         Assists Principal investigator in data interpretation and analyses

·         Reports on status of research activities.

·         Recruits study participants and ensures that subject recruitment and follow-up are completed per protocol procedures.

·         Orders and maintains inventory of supplies.

·         May assist in designing, developing, and modifying research experiments, procedures, or survey instruments. May assist research and support staff.

·         Performs additional functions incidental to research activities.



·         Min Dip/Deg in any discipline

·         1-2 years experience in clinical/lab research will be advantageous

·         Meticulous and efficient

·         Knowledge of Microsoft Excel

·         Excellent communication skills


If you are interested in any of the positions, do kindly drop your most updated resume to [ Email address blocked ]



Thank You.



Victoria Yam Wen Ting


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

  • Conducting a clinical research study
  • Participate in clinical research studies
  • Implement clinical research patient care via the research protocol
  • Impact clinical research patient charges
  • Resolve clinical research patient accounts
  • Ascertaining patient eligibility for clinical trials
  • Reviewing study protocols in the conduct of clinical research
  • Perform clinical research and coordinate research activities
  • Develop clinical study budgets based on proposed study protocols
  • Create informed consent forms for trials
  • Manage clinical research projects via study protocols and provide direct patient care for study participants
  • Visit clinical trial sites to ensure conformance with study protocol
  • Set up and maintain clinical databases per study protocol
  • Execute study visits and perform study procedures
  • Screen, consent and enroll patients into oncology clinical research trials
  • Determining eligibility of patients for clinical trials
  • Oversee clinical trials to meet regulatory requirements
  • Obtain informed consent, screen and enroll patient research subjects in suitable studies/clinical trials
  • Educate patients and family regarding particular study and clinical drug trials
  • Maintain clinical research professional credentials

Recommended Skills

  • Attention To Detail
  • Clinical Research
  • Clinical Trials
  • Clinical Works
  • Communication
  • Computer Terminals

EA License No.


EA Personal Registration No.

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