Clinical Research Pharmacist: Trials, Compliance & Impact

Recruit Express Pte Ltd

Singapore

Vor Ort

SGD 60.000 - 90.000

Vollzeit

14 Tage+

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Zusammenfassung

Recruit Express Pte Ltd is seeking a Clinical Research Pharmacist for a Pharma MNC in Singapore. This role covers planning, coordination, and conduct of clinical trials in line with study protocols and regulatory requirements, with office and project hours as needed.

You will work with clinical research teams, investigators, study coordinators, and sponsors to ensure medication safety and robust documentation. Strong communication and organizational skills are essential.

Qualifikationen

  • Bachelor's Degree in Pharmacy and registration is preferred.
  • Experience in clinical research or hospital pharmacy is advantageous.
  • Knowledge of ICH-GCP guidelines and trial regulations.

Aufgaben

  • Support the planning, coordination, and conduct of clinical trials in compliance with study protocols and regulatory requirements.
  • Ensure accurate documentation and maintenance of pharmacy-related clinical trial records.
  • Collaborate closely with clinical research teams, investigators, study coordinators, and sponsors.
  • Review study protocols and provide pharmaceutical expertise regarding medication management and patient safety.
  • Assist in site initiation, monitoring visits, audits, and inspections.
  • Support adverse event reporting and investigational product-related queries.
  • Maintain inventory control and proper storage conditions for study medications.
  • Participate in process improvement initiatives and clinical research projects.

Ausbildung

Bachelor's Degree in Pharmacy or equivalent

Jobbeschreibung

Recruit Express Pte Ltd is seeking a Clinical Research Pharmacist for a Pharma MNC in Singapore. This role covers planning, coordination, and conduct of clinical trials in line with study protocols and regulatory requirements, with office and project hours as needed.

You will work with clinical research teams, investigators, study coordinators, and sponsors to ensure medication safety and robust documentation. Strong communication and organizational skills are essential.

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