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The Clinical Scientist - General Medicine position plays a crucial role in the scientific planning and execution of clinical trials. This role involves assisting the Lead Clinical Scientist and the study team in the scientific conduct of clinical studies, providing an opportunity to develop leadership, technical skills, and scientific acumen as part of a global, cross-functional team. The position is hybrid, allowing for a combination of remote and on-site work, primarily based in North Wales, Pennsylvania, or Rahway, New Jersey. In this role, you will be responsible for specific clinical and scientific activities on one or more studies. This includes medical monitoring, lab specimen tracking and reconciliation, adjudication support, and preparation of meeting materials. You will also support the development of study protocols and related materials, such as informed consent forms and data management deliverables. Interaction with internal and external stakeholders, including country operations, committees, and vendors, will be essential to support clinical study objectives. Additionally, you will be involved in the development of training materials for sites and Clinical Research Associates (CRAs), prepare clinical narratives, and collaborate cross-functionally to monitor clinical study data, ensuring the quality, completeness, and integrity of trial conduct. Participation in Case Report Form (CRF) design will also be part of your responsibilities, ensuring that data collection aligns with the study protocol. This position requires a proactive approach to drive study goals and involves problem-solving, prioritization, conflict resolution, and critical thinking skills.