Clinical Development Scientist

Job Title
Clinical Development Scientist

Job Description

As Clinical Development Scientist you 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

The position is available in two locations: Haifa, Israel and Best, Netherlands

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

Proven medical writing skills for EU MDR clinical evaluation documentation

Experience transition from MDD to MDR

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

Experience communicating with notified bodies

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

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.

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If you’re interested in this role and have many, but not all, of the experiences needed, we encourage you to apply. You may still be the right candidate for this or other opportunities at Philips. Learn more about our commitment to diversity and inclusion here.

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