מציאת משרת הייטק בחברות הטובות ביותר מעולם לא הייתה קלה יותר
Asyou will develop the clinical evidence strategy, execution and dissemination in support of assigned CT-AMI programs. You will provide input to the cross-functional team through strong critical scientific thinking to develop innovative solutions for evidence strategy development.
Your role:
Leading development of evidence generation strategies of assigned projects, working within a cross-functional team
Creating subsequent clinical development / evaluation plans
Developing strong collaboration with KOLs and Investigators
Participate in the interpretation & dissemination of evidence generated from clinical evaluation plans such as Clinical Study Reports and Clinical Evaluation Reports
Supporting clinical evidence discussions with regulators, advisory boards, associations and societies
You're the right fit if you have:
MD, PhD / MS Degree in Science, or Bachelor’s Degree with equivalent experience
3-5 years of years’ experience in clinical research / development function, or related functional area
Strong scientific background and deep expertise in the development of clinical evaluation methods.
Deep knowledge and understanding of all applicable standards / regulations in clinical evidence generation and dissemination, including GCP, FDA requirements, EU MDR, NMPA, etc, and a broad understanding of the clinical operations required to execute evidence generation strategies
Proven ability to take independent action to initiate process improvement, when needed
Anticipates changing priorities and demands and addresses them proactively
Strong technology / therapeutic domain expertise with track record in successfully developing and executing clinical evidence plans
Manage clinical development associates and specialists on day to day clinical tasks and / or Subject matter expertise in relevant domain (technology / therapeutic area)
Strong ability to critically assess clinical literature
Excellent communication skills, including written communication (e.g., peer review publication) and oral presentation of scientific materials and research results. Ability to write original scientific documents such as clinical evaluation reports, clinical summaries, regulatory filings, investigator brochures, and internal reports and scientific publications.
We are a health technology company. We built our entire company around the belief that every human matters, and we won't stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work of your life to help the lives of others.
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