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Chiesi USA is a specialty pharmaceutical company focused on developing and promoting products for the hospital, adjacent specialty and rare disease markets. To achieve its mission of improving people’s quality of life by acting responsibly towards society and the environment, the Group research, develops and markets innovative drugs in its three therapeutic areas: AIR (products and services that promote respiration, from new-born to adult populations), RARE (treatment for patients with rare and ultra-rare diseases) and CAR E (products and services that support special care and consumer-facing self-care.
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Respond to questions from the research and development organization on an as-needed basis, including questions related to conduct of clinical trials in the United States and abroad. 8 – 10 years of relevant experience as a commercial product attorney for a pharmaceutical company and/or life sciences law firm.
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QualificationsRequired Skills 4+ years Clinical Database programming experience working in the biotechnology or pharmaceutical industry; experience working with CROs highly desirableTechnical/Software Skills: Expertise with Medidata RAVE (Custom Function programming) required.
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Prospect biotech and pharmaceutical companies seeking CGT process development and manufacturing partnerships that fit the ElevateBio BaseCamp strategic goals and objectives. This role is specifically focused on CMC partnerships in Cell and Gene Therapy in terms of process development, clinical and commercial manufacturing and will require a high level of engagement and collaboration.
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Seaport Therapeutics is a clinical–stage biopharmaceutical company advancing the development of novel neuropsychiatric medicines in areas of high unmet patient needs. PhD in Toxicology, Biology, Pharmacology, or other relevant field with minimum 12 years of professional/industry experience in toxicology–related research and/or drug discovery and development.
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REQUIRED: Masters in Public Health or in another Social Science discipline is desired OR a Bachelor's degree required with a minimum of five (5) years work experience in healthcare clinical research operations.
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Minimum of 10 years of specialty pharmaceutical/oncology/rare disease sales experience with a minimum 2 years of successful field management experience. We are proud to be the largest global pharmaceutical group to be awarded B Corp Certification, a recognition of high social and environmental standards.
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Aramco Services Company Petroleum Engineer: Thermodynamics Modeling (1344) Research & Development - Boston, MA - Full Time OVERVIEW: Performs and directs major projects related to the development of new thermodynamics-based models in reservoir simulation applications.
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Provide on-going clinical support to participants and staff in specialized programs as needed, providing on-going staff support using modalities such as MI, TIC, CBT, hoarding, solution-focused, harm reduction.
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Through research, education, clinical practice and community partnerships, we are committed to the mission of advancing health, providing each person the best care, in the right place, at the right time, every time.
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JOB SUMMARYThe Research RN, NCHRI works directly with the physician in accurately and professionally executing all clinical research projects in an acute care/inpatient setting (ED, Cath Lab, ICU, EP lab, Step down and OR) as well as the ambulatory and ancillary areas.
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Description The Process Research(PR) group within Synthetic Molecule Process Development (SMPD) is a global team responsible for interfacing with Takeda’s Discovery functions (e.g. medicinal chemistry, DMPK, Drug Safety) with the goal of route identification and phase appropriate route development to deliver GLP Tox and Ph 1 GMP Drug Substance (DS.
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The successful candidate will provide innovative administrative, clinical, research and educational leadership for the Division's expanding academic team. Tufts Medical Center is the principal teaching hospital of Tufts University School of Medicine and our close relationship with the School of Medicine allows the Chief and faculty access to the school's resources to build excellence in education and research, contributing to the school's missions of diversity, community impact, and health justice.
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Partner with other teams involved in the end-to-end assay launch and maintenance processes, including Clinical Ops, Clinical Lab, Quality, Regulatory Affairs, Medical, Business Stakeholders, etc.
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8+ years of regulatory affairs experience in drug development and product registration activities within the pharmaceutical or biotech industry in multiple phases of development; both big and small company experience is preferred.
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clinical research pharmaceutical company jobs Company: Qps Holdings in Somerville, MA
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