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The Clinical Sales Representative (CSR) will report to the Clinical Sales Manager with primary responsibility for delivering an excellent customer experience for all Galaxy customers within their territory. Our Clinical Sales Team is a dynamic and collaborative group committed to revolutionizing the
Our Clinical Sales Team is a dynamic and collaborative group committed to revolutionizing the field of robotic surgery by introducing groundbreaking solutions that contribute to improved patient outcomes, enhanced procedural efficiency. Provide strategic leadership to the sales team, fostering their
Partners closely with Clinical Development, Safety, Commercial, CMC, Quality, and Legal to ensure aligned and value-generating regulatory strategies. This role requires a highly strategic, scientifically grounded, and commercially savvy regulatory executive who can integrate complex development cons
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
Under the general supervision of a licensed care provider and/or management, the Clinical Medical Assistant I (CMA I)/ Patient Access Representative II (PAR II) is responsible to function as both a CMA I and a PAR II. The staff member is responsible for securing and providing appropriate medical bus
Under the general supervision of a licensed care provider and/or management, the Clinical Medical Assistant I (CMA I)/ Patient Access Representative II (PAR II) is responsible to function as both a CMA I and a PAR II. Per standardized clinical protocols, independently provides and documents clinical
Under the general supervision of a licensed care provider and/or management, the Clinical Medical Assistant I (CMA I)/ Patient Access Representative II (PAR II) is responsible to function as both a CMA I and a PAR II. This position utilizes appropriate age and developmental approaches in application
Under the general supervision of a licensed care provider and/or management, the Clinical Medical Assistant I (CMA I)/ Patient Access Representative II (PAR II) is responsible to function as both a CMA I and a PAR II. This position collaborates with interdisciplinary team to ensure optimal care is p
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. The Regulatory Af
A minimum of 10 years' in regulatory affairs leadership is required, along with significant experience in overseeing clinical operations and medical affairs. The Company is in search of a Vice President for Regulatory Affairs, Clinical Operations, and Medical Affairs. Vice President, Regulatory Affa
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
Serve as the Clinical QA lead for assigned clinical programs and provide quality oversight across all phases of clinical development to ensure compliance with ICH-GCP, applicable regulations, and Artiva's procedures. You'll represent Clinical QA on study teams, collaborating closely with all develop
This role involves providing medical expertise in the generation of safety reports, managing a team of medical safety professionals and PV scientists, and ensuring compliance with drug safety and pharmacovigilance regulations. The Executive Medical Director will also be involved in the oversight of
As we expand our in vivo research capabilities, including a variety of preclinical studies, we are seeking an experienced Director, GLP Quality Assurance & Compliance to establish and lead a Quality Assurance Unit (QAU). The Director, GLP Quality Assurance & Compliance will design, implement, and ov
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. Applicants must have a Doctor of Medicine (M
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
Standards Measurements Coordinates the measurement of the Joint Commission standards for the Provision of Care and National Patient Safety Goals Implements selected projects related to JC standards, National Patient Safety Goals and Nursing sensitive indicators. Using patient safety principles devel
Project Manager, Regulatory Affairs (Clinical and CMC). Join our team as a Project Manager in Regulatory Affairs, focusing on Clinical and CMC. This remote contract role involves leading cross-functional regulatory activities, enhancing project management standards, and mentoring junior project mana
Artiva is seeking an Associate Director, Clinical Quality Assurance to serve as the Clinical QA lead for assigned clinical programs and provide quality oversight across all phases of clinical development. Serve as the Clinical QA lead for assigned clinical programs and provide quality oversight acro
Partners closely with Clinical Development, Safety, Commercial, CMC, Quality, and Legal to ensure aligned and value-generating regulatory strategies. The Executive Director, Regulatory Strategy Endocrinology is a senior regulatory leader responsible for shaping and driving global regulatory strateg