Research Program Manager

1 week ago

Singapore beBeeStudy Full time

The role of Study Design Lead is a pivotal position that oversees the scientific and operational design of multi-country oncology research programs.

Key Responsibilities:

  • Scientific Communication & Publication : Develop study concepts, designs, and protocols for investigator-initiated trials and translational studies. Collaborate with PIs, scientific committees, and industry partners to define objectives, endpoints, and biomarker strategies.
  • Protocol & Feasibility Development : Draft and refine study protocols, synopses, schema, and feasibility questionnaires. Conduct feasibility assessments with participating sites, considering country-specific operational challenges.
  • Stakeholder Engagement : Serve as liaison between ATORG/APODDC leadership, site investigators, CROs, and vendors. Facilitate consensus meetings, advisory boards, and protocol review committees.
  • Quality Assurance Integration : Embed quality-by-design principles into protocol and operational workflows. Review study-specific operational, safety monitoring, and data management plans for compliance with international and local regulations, SOPs, and ethical standards.
  • Operational & Quality Oversight : Collaborate with Clinical Operations to ensure designs are executable within timelines and budgets. Support the development of safety monitoring, QA frameworks, and data management plans.

Required Skills & Qualifications:

  • A Master's or PhD in Life Sciences, Pharmacy, Public Health, or related field.
  • Formal training or certification in clinical research, medical writing, or biostatistics.
  • At least 7 years' experience in clinical research, with at least 3 years in study design, medical affairs, or scientific writing/publication roles.

Benefits:

  • Demonstrated success in designing and implementing multi-country investigator-initiated trials or equivalent academic-led research.
  • Prior experience working with multi-stakeholder research consortia, academic institutions, or industry collaborators in the Asia-Pacific region.

Advantageous Skills:

  • Scientific Writing & Communication: Excellent ability to translate complex scientific and clinical data into clear, accurate protocols, manuscripts, and presentations.
  • Analytical & Problem-Solving: Strong capability to evaluate scientific feasibility, identify risks, and propose practical solutions.

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