Pleryon招聘

职位描述：

• 一期临床试验
• 医学专业背景
• 药学专业背景

The Role: As Director of Clinical Affairs, you will drive the execution of a variety of clinical research programs, lead clinical operations and science teams, and have broad involvement central to pleryon's strategic clinical goals. Cross functional leadership tasks include early stage insights to products from a clinical perspective, collaborate with the business development on project strategy and liaise with the marketing ahead of conferences. You will be responsible for the management of research efforts, including KOL development and collaboration with the strategic partnership team. You will: • Lead the Clinical Affairs team and research function, achieving stated goals and ensuring that quality clinical studies are conducted per protocol, in a timely fashion, and in a manner compliant with SOPs, ICH/GCP/regulatory guidelines, company goals, and established study budgets • Be responsible for the execution of multiple clinical trials and research efforts, including ensuring the proper implementation of the clinical programs • Support study teams with start-up activities, enrollment, data collection, data reviews, database lock, etc. • Oversee ongoing and planned clinical projects, including but not limited to abstract submission, investigator meetings, and Scientific Advisory Boards • Collaborate internally with Strategy, R&D, Legal, and other internal teams to ensure clear cross-functional alignment, communication and execution You will love this job if: • You thrive in a fast-paced environment, juggling priorities, and exhibiting judgment to seek the best solutions • You are a strong project manager with attention to detail and experience translating detail to execution of clinical strategy • You are adept at discussing the science and research approaches critical for study protocol design, clinical endpoints, data interpretation and the intricate details of research operations • You have excellent scientific written and oral communication skills, as well as interpersonal, organizational, and clinical operations skills Requirements: • A minimum of 15 years experience in clinical research, operations and science within the ophthalmology and orthopedics field • Experience with clinical study design and clinical research operations • Experience with regulatory requirements governing clinical studies including US and Europe regulatory bodies

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Pleryon · HRBP