Director, Research Salary at Strategies 360 Inc BETA

Customer Facing Research Analyst Truveta is the world's first health provider led data platform with a vision of Saving Lives with Data. Our mission is to enable researchers to find cures faster, empower every clinician to be an expert, and help families make the most informed decisions about their care. Achieving Truveta' s ambitious vision requires an incredible team of talented and inspired people with a special combination of health, software and big data experience who share our company values. Truveta was born in the Pacific Northwest, but we have employees who live across the country. Our team enjoys the flexibility of a hybrid model and working from anywhere. In person attendance is required for two weeks during the year for Truveta Planning Week. For overall team productivity, we optimize meeting hours in the pacific time zone. We avoid scheduling recurring meetings that start after 3pm PT, however, ad hoc meetings occur between 8am-6pm Pacific time. #LI-remote Who We Need Tru

Position Description The University of Washington Department of Laboratory Medicine and Pathology has one (1) full-time academic position available at the rank of Open Rank without tenure (WOT) by reason of funding, with clinical duties at Seattle Children's Hospital. The Department of Laboratories at Seattle Childrens Hospital is recruiting a Medical Director of the Clinical Cell Processing Laboratory (CCPL), Associate Director of the Therapeutic Cell Production Core (TCPC), and Assistant Director of Transfusion Services. The CCPL is a clinical cell therapy lab supporting Seattle Childrens Hospital cellular products pipeline and the CCPL Medical Director is responsible for supporting the development of standard practices and FACT accreditation and ensuring medical safety and regulatory compliance of the CCPL. The CCPL Medical Director will be responsible for working with clinical and research teams to maximize impact and safety, oversee clinical operational aspects of the CCPL and ser

Company We are a Global Business leading the market with Australian made and owned dental restorative products, teeth whitening and small equipment. Founded in 1972, SDI products are now distributed in over 100 countries throughout the world. Our global head office and manufacturing plant is located in Melbourne with overseas branch offices and warehousing in the USA, Brazil and Germany. The ideal candidate will have had experience working in the dental industry, a medical devices company or a dental office (Hygienist). A clinician working in dental office with some sales experience is the preferred candidate for this role. Summary of Role The Territory Sales Manager is responsible for: Meeting or exceeding sales targets within the territory with a focus on achieving Hero product targets Aligning sales objectives with SDI's strategic priorities Building business relationships with dentists and their dental office teams, distributor sales teams, dental schools, community health centres

We are looking for talented Medical Laboratory Scientist to join our team. As a Medical Laboratory Scientist, you will be instrumental in advancing our diagnostic capabilities, particularly focusing on ELISA-like technologies. This role requires a dynamic individual ready to engage both in research development and CLIA laboratory settings, ensuring the highest quality of our Laboratory Developed Tests (LDTs). Key Responsibilities: Lead the development refinement of SOPs across all laboratory processes. Spreadhead the laboratory quality management system, fostering a culture of continuous improvement. Oversee validation and verification studies for advanced diagnostic methods. Uphold stringent laboratory procedures, ensuring compliance with regulatory standards. Drive quality control initiatives, maintain rigorous documentation and adherence to policies. Execute instrument maintenance, calibration, and qualification with meticulous attention to detail. Analyze Quality Indicators and app

**Research Associate II, Editing Strategy** Are you a highly motivated, collaborative, and scientifically curious individual? If so, we're seeking you, and your bold ideas, to co-lead and accelerate the development of our research programs for patients in need. Here, at Astellas, we are a driven bunch with a passion for testing the capabilities of iPSC-derived cells and for developing them into transformational therapies. If you want to be part of this exciting work, you belong at Astellas! Astellas Pharma Inc. is a pharmaceutical company conducting business in more than 70 countries around the world. We are committed to turning innovative science into medical solutions that bring value and hope to patients and their families. Keeping our focus on addressing unmet medical needs and conducting our business with ethics and integrity enables us to improve the health of people throughout the world. For more information on Astellas, please visit our website at www.astellas.com. Universal Ce

Etz Hayim owns and operates the brands Cycling Frog and Lazarus Naturals, as well as a sprawling operation that spans from farming over 300 acres of hemp, extraction, chemical processing, packaging and warehousing to support both brands and private label customers. Lazarus Naturals was founded in 2016 to provide safe and accessible CBD products for everyone who would benefit from them, regardless of their financial situation and ability to pay, which is why we provide a 60% Assistance Program to veterans and people with disabilities or low-incomes. In order to maintain an affordable price point and our commitment to accessibility for all, we have built a vertically integrated business model, which allows us to walk our talk of developing quality, affordable products - from product inception, development, seed, farming, extraction, finished production formulation and packaging, and distribution. Cycling Frog is normalizing the consumption of casual use THC products. We are on a mission

1. Job Purpose: This position is responsible for project management and study site management from site selection to initiation until monitoring and close-out of assigned clinical study studies in accordance with Tigermed or sponsor Standard Operating Procedures (SOPs), International Conference on Harmonization Good Clinical Practice standard (ICH-GCP), Clinical Practice standard (GCP) and other applicable regulations; The position is responsible for ensuring that all data generated by the assigned sites is of high quality, on time and within budget. 2. Responsibilities: Planning of project activities and study timelines based on project goal and sponsor's expectation; Organize and Lead meeting/teleconferences for study activities implementation (e.g. investigator meeting, project review meeting etc), monitoring the progress of each CRA responsible sites, and assessing overall status of the project; Develop the project management plan, monitoring plan etc as required for the study; Dev

Study Director - Research Scientist Your New Company! At our CRO, we move in unison to assist and contribute to the discovery, development, and manufacturing of new drug therapies to bring them faster to the people who need them. Regardless of your role, you will play an essential part in impacting health and well-being globally. By fostering our core values—Employee Development, Customer Focus, Quality and Excellence, Respect, and Integrity—we create a passionate and collaborative work environment. If you’re a recent graduate or a seasoned professional seeking your next career opportunity, it’s time to discover your future with us. About the Role As a Study Director, Research Scientist, your passion for preclinical research will shine as you act as the single point of control for assigned GLP and non-GLP studies. You’ll ensure the interpretation, analysis, documentation, and reporting of study results are accurate and impactful. Key Responsibilities Oversee the technical conduct of st