Clinical Research Physician (Hematology)

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Responsibilities:

  • Support medical director in drafting clinical trial protocol and study report.
  • Contribute to the medical/scientific input given for the development of trial-related documents such as IB, ICF etc. and processes which reside in other line functions.
  • Establish and maintain liaisons with investigators.
  • Serve as back-up medical monitor to provide medical support to trial sites and clinical operation team.
  • Support regulatory filing where medical expertise is required.
  •  Support drug discovery when clinical experience is needed for the medical “translation”.
  • Lead clinical trial data review and generate clinical queries, quality control and data validation for clinical study reports, publications and internal/external presentations.
  • Prepare and conduct regular meetings with investigators.
  • Support clinical study site and CRO selection in trial conduct and clinical trial outsourcing process.
  • Support the regional clinical strategy for a project through Clinical development, in partnership with relevant matrix team members.
  • Compliance with GCP, SOP and regulatory requirements.
  • Study planning, preparation, conduct and report in terms of timeline, quality and quantity
    ( recruitment target ).
  • Other tasks as assigned.

Requirements:

Education: Graduate from Clinical Medicine with bachelor degree or above.

Experience: At least 3-5 year clinical practice / clinical development / clinical research experience. Therapeutic area experience esp. oncology or hematology. Working experience with international pharmaceutical company or CRO is preferable.
GCP experience is preferred.

Skills: Proficiency in English and good computer skill at office software.
Excellent planning, organization and problem solving abilities.
Good communication and interpersonal skills.

Competency: Good project management skill.
Self-motivation and good risk management.