Clinical development scientist at Philips

Best, North Brabant, Netherlands -

Full Time

Start Date

Immediate

Expiry Date

05 Apr, 26

Salary

0.0

Posted On

05 Jan, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical Research, Evidence Generation, Medical Writing, Regulatory Knowledge, Collaboration, Scientific Thinking, Clinical Evaluation, Communication Skills, Critical Assessment, Clinical Study Setup, KOL Engagement, Data Interpretation, GCP Knowledge, FDA Requirements, EU MDR, NMPA Knowledge

Industry

Hospitals and Health Care

Description

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 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 (Key Opinon Leaders) 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. Experience with setting up clinical study and involvement in clinical research in the medical device industry Proven medical writing skills with a strong ability to critically assess clinical literature. We are open for people with a pharma/IVD/biotechnology medical writing experience background. 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 (National Medical Products Administration), etc., and a broad understanding of the clinical operations required to execute evidence generation strategies. Experience communicating with notified bodies is a preference. Excellent communication skills, including written communication (e.g., peer review publication) and oral presentation of scientific materials and research results. How we work together We believe that we are better together than apart. For this role, this means working in-person at least 3 days per week. About Philips 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. • Learn more about our business. • Discover our rich and exciting history. • Learn more about our purpose. 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 culture of impact with care here. #LI-EU At Philips, we believe that every human matters. As a global health-tech leader, we focus on improving people’s health and wellbeing through meaningful innovation. The people who work here share our passion and are motivated to bring this purpose to life. For more than 130 years, we have been creating technologies and innovations that improve people's lives and support healthcare practitioners. Headquartered in the Netherlands and operating in more than 100 countries globally, we focus our advanced technology and deep clinical and consumer insights on Precision Diagnosis, Image Guided Therapy, Enterprise Informatics, Monitoring/ Connected Care, Sleep & Respiratory Care and Personal Health. Together, we deliver better care for more people because we believe that every human matters. That's why we're taking steps to create an environment where we acknowledge and embrace our differences and uniqueness and listen to and value each other's views. When people feel cared for and listened to, they bring their best qualities to work, leading to better collaboration, communication, innovation and success. It is the policy of Philips to provide equal employment and advancement opportunities to all qualified employees and applicants for employment without regard to race, color, religion, sex, pregnancy/childbirth or related medical conditions, age, ethnic or national origin, sexual orientation, gender identity or expression, physical or mental disability, genetic information, citizenship status, veteran or military status, marital or domestic partner status or any other characteristic protected by law. As an equal opportunity employer, Philips is committed to fostering a culture where all are treated with respect and professionalism. To ensure reasonable accommodations for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Veterans' Readjustment Act of 1974 and Title I of the Americans with Disabilities Act of 1990, applicants that require accommodation in the job application process may contact 888-367-7223, option 5, for assistance. Philips is an Equal Employment and Opportunity Employer including Disability/Vets and maintains a drug-free workplace. Know Your Rights

Responsibilities

The Clinical Development Scientist will lead the development of evidence generation strategies and create clinical development plans. They will collaborate with cross-functional teams and engage with Key Opinion Leaders and investigators to support clinical evidence discussions.