Senior Clinical Development Scientist, CT — Evidence & Submissions

Philips International; Connecticut; Hybrid; USD 91,000 - 151,000; Full time

Job summary

Philips is seeking a Senior Clinical Development Scientist in Connecticut to analyze clinical studies, ensure regulatory compliance, and develop high-quality CERs, CSRs, and PMCF documents. You will collaborate with cross-functional teams to drive evidence-based insights and support regulatory submissions.

The role requires深 experience in clinical development for medical devices, biostatistics, and strong English communication, with onsite collaboration and global teamwork.

Qualifications

• 5+ years of experience in Clinical Affairs, Clinical Research, or a similar role within the Medical Device, Pharmaceutical, or Healthcare industry.
• Strong understanding of EU Medical Device Regulations, Good Clinical Practice (GCP), and ICH guidelines; experience with clinical investigation design, biostatistics, research methodologies, medical and scientific literature databases, and medical writing.
• Experience applying statistical methods to clinical data and proficiency with statistical software is preferred.

Responsibilities

• Collect, appraise and analyze clinical data pertaining to a medical device. Write documentation such as CERs and PMCF reports to support regulatory submission.
• Collaborate with internal and external partners to ensure comprehensive analysis of clinical evidence and dissemination of results.
• Create procedures and workflows related to the Clinical Development department.

Skills

Clinical research

Regulatory compliance

Project management

English proficiency

Statistical software

Education

MSc/PhD/MD/PharmD in Biomedical Sciences or related

Tools

Statistical software

Job description

Philips is seeking a Senior Clinical Development Scientist in Connecticut to analyze clinical studies, ensure regulatory compliance, and develop high-quality CERs, CSRs, and PMCF documents. You will collaborate with cross-functional teams to drive evidence-based insights and support regulatory submissions.

The role requires深 experience in clinical development for medical devices, biostatistics, and strong English communication, with onsite collaboration and global teamwork.