Collecting information
Organizing data
Experience in healthcare/medical device sales a plus. Brings in clinical specialist to educates prospects about STISIM's solutions and capabilities. Sales Operations & Process – 20%.
The Executive Director, Regulatory Strategy – Endocrinology is a senior regulatory leader responsible for shaping and driving global regulatory strategy across Company’s Endocrinology pipeline, spanning early development through commercialization. This role requires a highly strategic, scientifi
Responsible for the regulatory CMC leadership of one or more commercial and development projects, including responsibility for regulatory strategy, IND/CTA preparation, maintenance and update activities, interaction with and preparation for key milestone meetings with regulatory agencies with focus
Medical Billing Specialist (Revenue Cycle Management) – Bilingual Spanish Preferred. Proficiency with EMR/EHR systems. Medical Billing Specialist with demonstrated.
The ideal candidate will have prior experience as a medical monitor on Phase I-IV clinical trials in a pharmaceutical, biotechnology, or CRO setting, and possess a strong knowledge of clinical trial methodology, safety assessment, and medical data review. A minimum of 10-15 years' of experience in c
The Executive Director, Regulatory Strategy Endocrinology is a senior regulatory leader responsible for shaping and driving global regulatory strategy across Company's Endocrinology pipeline, spanning early development through commercialization. This role requires a highly strategic, scientifically
We are seeking an experienced Project Manager to lead a cross-functional medical device development program covering firmware updates, PC software development, hardware qualification, and manufacturing release. Proven experience managing projects in regulated environments (medical devices, healthcar
Specific responsibilities will include: being the clinical or program lead for the development of clinical research strategies, clinical development plans, and independent direction of Phase 1-4 clinical studies collaboratively within cross-functional project teams (including clinical operations, pr
Experience in healthcare, life sciences, or biopharma in a business development, commercial, or strategic sales role. By developing tailored engagement plans, building trusted relationships, and orchestrating multi-functional solution development, the Director, Regional BD drives both immediate impa
Clinical/Medical Lab Scientists. Clinical/Medical Lab Scientists are highly skilled scientists who discover the presence or absence of disease and provide data that help physicians determine the best treatment for the patient. Clinical/Medical Lab Scientist generally work in a lab setting.
To qualify for the Regulatory Affairs Specialist III role, candidates must have a Bachelor's degree in life sciences, engineering, or a related field, along with at least 6 years of experience in a regulated environment, including 4 years of direct experience in Regulatory Affairs. Regulatory Affair
Note: Must have Medical Devices domain only Role Overview: We are seeking an experienced Project Manager to lead a cross-functional medical device development program covering firmware updates, PC software development, hardware qualification, and manufacturing release. Project Manager Embedded Syst
The Medical Director will work in close partnership with cross-functional teams including Clinical Operations, Regulatory Affairs, Biostatistics, Safety/Pharmacovigilance, Translational Medicine, and Medical Affairs. This role provides medical leadership across one or more clinical development progr
Responsible for the regulatory CMC leadership of one or more commercial and development projects, including responsibility for regulatory strategy, IND/CTA preparation, maintenance and update activities, interaction with and preparation for key milestone meetings with regulatory agencies with focus
Regulatory Affairs, Licensing and Accreditation Supports multi?hospital regulatory readiness and ongoing compliance with Joint Commission, CDPH, CMS, and other applicable regulatory and accreditation agencies. The Senior SpecialistPerformance Improvement-Licensing and Accreditation is responsible fo
Vice President, Regulatory Affairs, Clinical Operations & Medical Affairs. The Company is in search of a Vice President for Regulatory Affairs, Clinical Operations, and Medical Affairs. A minimum of 10 years' in regulatory affairs leadership is required, along with significant experience in overseei
Employee share purchase scheme Bi-annual Profit share Life, Critical illness and Income Protection Insurance Discounted Health Insurance Active Social clubs & community groups In-house training programs from external providers Purchasing privileges for Fisher & Paykel Healthcare and Medela pro
Project Manager, Regulatory Affairs (Clinical and CMC). Join our team as a Project Manager in Regulatory Affairs, focusing on Clinical and CMC. Project Management Tools | Regulatory/Document Systems | Collaboration Tools | AI Tools.