We are supporting a life sciences organization with a regulatory systems modernization initiative and are seeking an experienced Regulatory Publishing professional to support submission data alignment and future-state readiness activities. · This role is highly execution-focused ...

We are supporting a life sciences organization with a regulatory systems modernization initiative and are seeking an experienced Regulatory Publishing professional to support submission data alignment and future-state readiness activities. · This role is highly execution-focused ...

+The Cortex team within the Department of Neurology at BIDMC provides world-class care and engages in clinical trials for patients with neurological disorders and conditions such as Parkinson's disease, Alzheimer's disease, Huntington's disease, epilepsy, stroke, neuromuscular di ...

Join the growing BILH team at Beth Israel Deaconess Medical Center in Boston MA as a Regulatory Specialist working full-time day shifts. · ...

The regulatory specialist will report directly to the Cortex Program Manager and will work with faculty and study teams to support high quality and compliant conduction of clinical trials in the Department. · This includes offering clinical research expertise in reviewing and imp ...

This job involves preparing regulatory submissions while ensuring compliance with current regulations. The specialist will maintain meticulous regulatory documentation. · Proficiency in Regulatory Documentation. · Strong understanding of Regulatory Compliance. · ...

We are seeking a Regulatory Affairs Specialist to join our Global Regulatory Affairs Team. The ideal candidate will have experience in regulatory affairs and a passion for driving innovative solutions. · ...

We believe there is a smarter, more data-driven way to make decisions in healthcare and our cloud-native AI powered SOPHiA DDM Platform makes that vision a reality on a daily basis.You will have direct input to our mission to democratize data-driven medicine for the ultimate bene ...

+Will guide investigators in the IRB review process and will assist with the preparation and submission of protocol documents to the IRB and other regulatory committees to ensure regulatory compliance. · Bachelor's Degree Related Field of Study required or Master's Degree Related ...

The Research Regulatory Specialist provides regulatory compliance activities for clinical research studies.This position ensures that all regulatory documentation is accurately prepared, maintained, and submitted following the ICH Good Clinical Practice (ICH GCP), FDA, IRB, · and ...

This position will guide investigators through the IRB review process and assist with the preparation and submission of protocol documents to the IRB · and other regulatory committees, ensuring regulatory compliance. · Advising researchers and research teams on the requirements ...

+Be part of a Regulatory Affairs Team to develop and deploy innovative and compliant regulatory strategies across business and markets to achieve the highest standards for patient safety and product efficacy.+Assist in the implementation of comprehensive regulatory strategies by ...

Job Summary · Summary: This position will guide investigators through the IRB review process and assist with the preparation and submission of protocol documents to the IRB and other regulatory committees, ensuring regulatory compliance. Responsible for supporting the implementat ...

We are looking for a Regulatory Affairs Specialist to join our team in Cambridge, MA. In this role you will assist in implementing comprehensive regulatory strategies by collaborating with regulatory subject matter experts (SMEs) to ensure alignment with company objectives and co ...

We are seeking a Clinical Regulatory Specialist to join our team at Iterative Health. · Assisting research sites with the conduct and compliance of Phase 2-4 pharma-sponsored research studies. · ...

We are seeking a Clinical Regulatory Specialist to join our team. The Clinical Regulatory Specialist will work under the direction of the Chief of Staff with the primary responsibility of assisting research sites with the conduct and compliance of Phase 2-4 pharma-sponsored resea ...

In this role you be part of a Regulatory Affairs Team to develop and deploy innovative and compliant regulatory strategies across business and markets to achieve the highest standards for patient safety and product efficacy. · ...

Be part of a Regulatory Affairs Team to develop and deploy innovative and compliant regulatory strategies across business and markets to achieve the highest standards for patient safety and product efficacy. · Assist in the implementation of comprehensive regulatory strategies by ...

We are seeking a Regulatory Affairs Specialist to support the Life Cycle Management (LCM) Regulatory Affairs team in the creation,maintenance,and review of technical documentation.This role ensures compliance with European and U.S.medical device regulations,includingsuch as EU MD ...

The Sr. Regulatory Affairs Specialist is responsible for supporting DeepHealth's product and product development and regulatory activities to commercialize new digital products including AI technologies. · ...

We are looking for a Regulatory Affairs Specialist to develop and deploy innovative and compliant regulatory strategies across business and markets. · Assist in implementing comprehensive regulatory strategies by collaborating with regulatory subject matter experts (SMEs). · Coor ...