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- 게시됨
- 3일 전
직무 설명
Role overview
This position is for a pharmaceutical research specialist who can create detailed enterprise research workflows and realistic operational scenarios within regulated R&D settings. The work focuses on making clinical and scientific processes feel authentic, structured, and suitable for evaluation.
Key responsibilities
- Develop realistic pharmaceutical research environments that mirror cross-functional R&D operations and documentation practices.
- Construct multi-stage scenarios covering clinical, regulatory, translational, and drug development activities.
- Design structured task sequences that involve research platforms, technical documentation, protocols, and coordination among stakeholders.
- Work with subject matter experts to improve the realism of workflows, evaluation criteria, and the level of operational detail.
- Bring domain knowledge from areas such as drug discovery, clinical development, regulatory affairs, CMC, and pharmacovigilance.
Candidate profile
- A solid background in pharmaceutical, biotech, or translational research environments is expected.
- Prior exposure to regulated R&D workflows, clinical operations, or scientific documentation processes is important.
- Comfort using research and clinical systems commonly found in enterprise pharmaceutical settings.
- Ability to break down complex scientific and operational processes into clear, process-based task scenarios.
- Strong analytical ability, technical writing skills, and a collaborative working style are needed.
Engagement details
This is a flexible remote contract role with competitive hourly compensation based on domain expertise. The work is ongoing and project-based.
Application process
Selected candidates will be contacted with the next steps after applying.