Clinical Scientist Salary at Merz Aesthetics BETA

Job Description Job Description We are looking for a Clinical Trials Project Manager II to join our team! APPLY DIRECTLY at https://cpcclinicalresearch.org/careers/ (internal title Clinical Operations Manager II) Are you well organized, but adaptable to unexpected changes? Someone who is able to see the bigger picture, without losing sight of the day-to-day tasks? If the answer is yes, keep reading! This role serves as the primary point of contact for industry sponsored clinical trials and Endpoint and Specialty Services activities. In this position you will: Oversee clinical operations management activities Define and monitor project scope, timelines and deliverables from project initiation to close-out. Identify project-specific training for team members and notify appropriate designee to ensure completion and filing of training documentation. Oversee trial-related activities. Track and approve vendor payments. Provide expert advice in the design, writing and/or review of all project

Research Assistant Morrisville, North Carolina Our client is a GLP contract research laboratory that designs and conducts customized in vitro and in vivo laboratory services for any research and method development need. Their team of scientists, researchers, and technicians offer innovative and practical approaches with the flexibility of academia but with GLP quality and unmatched efficiency. Essential functions: Rodent dosing (oral gavage, i.p, subQ, i.v.) Clinical observations and body weights Necropsies Tissue/blood sample collection and processing Support conduct of GLP in vitro and in vivo studies Study data documentation under GLP guidelines All duties performed on an as-needed basis Preferred Experience: At least 1 year of college level biology education At least 2 years of GLP laboratory experience Ability to work standing or sitting for long periods at a time Very strong work ethic Ability to follow instructions Works well as part of a team Excellent time management skills wi

About Us Founded in 1908, Merz is a successful, family-owned specialty healthcare company with a rich history. As a leading global aesthetics business, our award-winning portfolio of injectables, devices, and skincare products empowers healthcare professionals to enhance confidence through aesthetic medicine. Our purpose is to fuel confidence by helping people look better, feel better, and live better. We believe you do not have to choose between living life and making a living. Live your best life with Merz Aesthetics. A brief Summary Serves a key role within the Merz Aesthetics Clinical Research and Development team, the Global Head of Clinical Development will be responsible for the development and implementation of clinical strategies for new innovative medical devices and new substances across the US and EU Clinical Development teams. Accountability for clinical aspects of Product Development from early evaluation through design and conduct of clinical studies, post-market studies

About SpringWorks Therapeutics: SpringWorks is a commercial-stage biopharmaceutical company applying a precision medicine approach to developing and delivering life-changing medicines for people with severe rare diseases and cancer. SpringWorks has a diversified targeted oncology pipeline spanning solid tumors and hematological cancers, including clinical trials in rare tumor types and highly prevalent, genetically defined cancers. SpringWorks' strategic approach and operational excellence in clinical development have enabled it to rapidly advance its lead product candidates into late-stage trials and enter into multiple collaborations with innovators in industry and academia to unlock the full potential for its portfolio and create more solutions for patients with cancer. Your Role: Reporting to the Vice President, Biology Research, the Translational Medicine Laboratory Senior Scientist I, will serve as a direct scientific contributor to Translational Medicine project teams, facilitat

Locus Biosciences is seeking a highly motivated and entrepreneurial applicant to join our company in a full-time, entry-level position that will rotate between our Chemistry, Manufacturing and Controls (CMC) and Research & Development (R&D) departments in the first year. This position is well suited for those looking for an entry-level position that is excited to learn all aspects of biotechnology drug development from early-stage research through drug product manufacturing. Candidates will be expected to accomplish defined work, as well as assist in approaching and solving complex scientific problems. Candidates should have demonstrated laboratory or manufacturing experience, with solid communication, technical aptitude, and problem-solving skills. Experience working in regulated, pharmaceutical/biotechnology R&D (GDP, GLP) and/or manufacturing environments (cGMP) is strongly preferred, but not required. Why Locus? Change the future of medicine and address a serious and unmet patient

Position Overview The Engineer / Scientist 3, Downstream MSAT will provide tech transfer support and technical oversight for large scale purification activities for Monoclonal antibody production. Follow Your Genki to North America's largest, state-of-the-art Life Science Manufacturing Facility & CDMO The work we do at FUJIFILM Diosynth Biotechnologies has never been more important—and we are looking for talented candidates to join us. We are growing our locations, our capabilities, and our teams, and looking for passionate, mission-driven people like you who want to make a real difference in people’s lives. Join FUJIFILM Diosynth Biotechnologies and help manufacture the next vaccine, cure, or gene therapy in partnership with some of the most innovative biopharma companies across the globe. We are proud to cultivate a culture that will fuel your passion, energy and drive - what we call Genki. Join us We are growing our locations and are investing more than $2 billion into establishing

Join us in developing pioneering therapies that aim to transform the treatment of CKD and change patients' lives. Our technology is designed to treat diseased kidneys using a patient's own cells and may prevent or delay dialysis or transplant. We are seeking a highly skilled and motivated Senior Scientist - Translational Biology to support mechanism of action elucidation for rilparencel, our autologous kidney cell therapy currently being evaluated in a Phase 3 clinical study, as well as the development of next-generation cell therapies by leading high-depth analytical study design & characterization of both in vitro & in vivo models. This role will focus on applying state-of-the-art multi-omic approaches - including single-cell RNA sequencing (scRNA-Seq), spatial transcriptomics, single cell epigenomics, metabolomics, lipidomics, proteomics, CITE-Seq, and CyTOF - to advance our understanding of cell therapy mechanisms of action, persistence, potency, and safety. The ideal candidate wil

R&D Partners is seeking to hire an Associate Stability Research Scientist II in Clayton, NC. Your main responsibilities as a n Associate Stability Research Scientist II: · Daily, maintain product inventory for active stability studies in accordance with all compliance requirements by assuring the accountability and delivery of all stability samples and associated documentation as well as the issuance of required documentation for testing. · Coordinate with Packaging to acquire samples for batches to be placed into the stability program for evaluation. · Maintain label printers in good working order to ensure ability to fulfill printing of labels for stability requests. · Maintain and audit all sample labeling and documentation for accuracy and compliance with GMP. · Facilitate delivery of stability samples for laboratory testing and coordinate with QC Sample Specialists and stability supervisors to correct any discrepancies associated with stability samples for testing. What we are loo