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Clinical Research Associate / Clinical Trials Assistant (No exp needed, Training Provided)


Job Description

Clinical Research Coordinator



  • Supports enrolling patients onto clinical trials through recruitment, screening, enrollment and follow up of eligible subjects according to protocol requirements.
  • Responsible for working with the principal investigator to meet or exceed study enrollment.
  • Reviews the study design and inclusion/exclusion criteria with physician and patient.
  • Ensures the protection of study patients by verifying informed consent procedures and adheres to protocol requirements/compliance.
  • Ensures the integrity of the data submitted on Case Report Forms or other data collection tools by careful source document review. Monitors data for missing or implausible data.
  • Ensures that adequate and accurate records are maintained for inspecting.
  • Creates study specific tools for source documentation when not provided by sponsor.
  • Collects, completes, and enters data into study specific case report forms or electronic data capture systems.
  • Generates and tracks drug shipments and supplies as needed.
  • Reports and follows up on serious adverse events as necessary.
  • Implements study-specific communications.
  • Ensures timely adherence to protocol requirements.
  • Responsible for completion of all required documentation according to site works guidelines.
  • Ensures timely and accurate data completion.
  • Maintains accurate and complete records including regulatory documents when applicable, signed informed consent forms, source documentation, drug dispensing logs, subject logs and study-related communications.
  • Tracks and reports adverse events, serious adverse events, protocol waivers, deviations, and violations.
  • Communicates all protocol-related issues to appropriate study personnel or manager.
  • Attends study specific on site meetings, Investigator meetings, conference calls and monthly CRC meetings as required or asked to do so.
  • Apprises principal investigator, Research Operations Director and Regional site manager of all study specific medical issues for guidance.
  • Maintains patient confidentiality according to ethical and legal requirements.
  • Assists in providing coverage for satellite clinic sites as necessary or asked to do so.
  • Practice and adhere to the 'Code of Conduct' philosophy and 'Mission and Value Statement.'




  • Min Degree, preferably in Science / Life Sciences / Public Health / Health Sciences / Pharmacy / Medicine / Nursing or similar from an accredited university
  • No exp needed, full training provided
  • At least 1-2 years of working experience within clinical research settings (e.g. clinical research associate, study coordinator, or research administrator) is advantageous but not essential
  • Knowledge of GCP guidelines and applicable regulations and guidelines of clinical research, or ethical principles relating to human biomedical research
  • Able to work independently, as well as part of a team
  • Able to work with a high degree of accuracy and attention to detail
  • Possess excellent analytical, organisation, communication, and interpersonal skills


If you are interested in the position, 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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Employment Type

Contract / Temp


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