Strong technical skills and experience in commercial biopharmaceutical Quality/Manufacturing in the areas of microbiology, environmental monitoring, microbiological testing, cell culture and/or purification, engineering or validation. At Takeda, we are transforming patient care through the developme...
The Senior Manager, Data Management acts as the Lead Data Manager for multiple clinical studies and/or a clinical development program.They provide leadership and guidance for all phases of clinical studies from the EDC study design through to study closeout.They will be responsible for the oversight...
Corbus Pharmaceuticals Holdings, Inc. ...
The Field Reimbursement Manager (FRM) helps minimize access & reimbursement barriers for patients and providers to optimize access to Apellis' Ophthalmology portfolio.Within their geography, the FRM is responsible for addressing access barriers by strategically working with customers and accounts to...
We are seeking an attorney to join our innovative and close-knit Legal and Compliance team at Deciphera Pharmaceuticals. The position uniquely offers the opportunity to support company-wide needs at a growing, global, commercial biopharmaceutical company with one approved product (QINLOCK®) in the U...
The Director Trial Master File (TMF) and Clinical Documentation spearheads the vision and strategy for records management of clinical trial documents.They are accountable for leadership of the TMF organization, including technology and systems, TMF Operations, TMF inspection readiness, outsourcing a...
Deciphera is a biopharmaceutical company focused on discovering, developing and commercializing important new medicines to improve the lives of people with cancer. Safety with development and marketed products in a biopharmaceutical industry setting. ...
As part of the Research and Development leadership team, collaborate with the pharmaceutical research, clinical development, isotope strategy and regulatory departments to support the planning, execution, and management of clinical trials activities. Minimum of 12 years of medical affairs or clinica...
Deciphera is a biopharmaceutical company focused on discovering, developing and commercializing important new medicines to improve the lives of people with cancer. ...
Participate in the development and maintenance of global clinical data standards.Act as an expert on operational data standards, (SDTM & ADaM) standards, and CDISC controlled terminology.Provide guidance to Study Teams and Submission Teams on SDTM/ADaM standards and related submission requiremen...
Minimum of 5 years experience in pharmaceutical, immunology, biologic/biotech, or medical device industries. Health care business acumen with a comprehensive understanding of the pharmaceutical industry desired. At Takeda, we are transforming patient care through the development of novel specialty p...
Deciphera is a biopharmaceutical company focused on discovering, developing and commercializing important new medicines to improve the lives of people with cancer. The Senior Manager, Pharmacovigilance (PV) Quality encompasses a key leadership role in providing direction to the PV department and pro...
We help make your world a safer place.Securitas is a global company that offers the most advanced and sustainable security solutions in the industry.We are located in 47 countries and have 355,000 employees worldwide and over 150,000 clients.Securitas plays an essential role for our clients and in s...
BS/BA or higher degree or an equivalent combination of education and experience in related field of pharmaceutical or biopharmaceutical industry. Be Seen and Heard at EyePoint Pharmaceuticals. This position provides production support for analytical quality control testing of pharmaceutical raw mate...
Qualifications and Skills Bachelor's or master's degree in Accounting, Finance, or a related field CPA certification is strongly preferred 8+ years of progressive tax experience, including a background in a Big Four accounting firm, within the bio-tech, pharmaceutical, or life sciences industry stro...
We are seeking a Chemical Engineer experienced in small molecule Drug Substance and Drug Product process development and commercial manufacturing to join our Pharmaceutical Development and Manufacturing team. The candidate should also have a command of chemical synthesis and purification for small m...
This position is to support the Global Patient Safety (GPS) department in business support of safety systems utilized for pharmacovigilance.This includes overseeing daily activities such as generating searches and output in support of departmental data requests, internal audits, and health authority...
The Senior Manager of Pharmaceutical Strategic Business Insights will administer, manage, and optimize financial and operational performance of initiatives that promote the advancement of CVS Health’s long-term strategies across the pharmaceutical landscape. ...
This position is responsible for supporting the quality & compliance activities associated with Global Patient Safety (GPS).Such activities include developing, performing, trending and analyzing quality and compliance metrics and associated outputs related to Safety Sciences Quality & Compliance del...
PhD in biochemistry, biological science, or chemical engineering or related fields with 4+ years of relevant experience, or BS/MS with 8+years of relevant experience in biopharmaceutical organization with expertise in drug substance/drug product development and/or tech transfer. ...
This role is a hybrid position which means the individual must work on-site 3 days per week.Fully remote work is not possible for this role.The position can be based in Armonk, NY, Basking Ridge, NJ or Uxbridge, England.The Clinical Study Specialist (CSS) provides technical and administrative suppor...
The Senior Research Associate will be a key player in driving genomic medicine pipeline project through target validation, candidate selection and IND-enabling phases using in vitro, in vivo and ex vivo studies.Important aspects of this role include excellent organization skills, flexibility, and th...
Understanding of pharmaceutical clinical development across multiple therapeutic areas (i. Bachelor's in Statistics, Computer Science, Mathematics, Engineering, Life Science or related field with 8+ years of programming experience preferably in processing clinical trial data in the biotechnology, ph...
The Senior Manager, Global Procurement will report to the Senior Director, Global Procurement, International Markets and is responsible for developing and driving strategy for our procurement activities within UK & France as part of Regeneron’s international footprint.They work collaboratively with ...
Understanding of pharmaceutical clinical development across multiple therapeutic areas (i. Bachelor's in Statistics, Computer Science, Mathematics, Engineering, Life Science or related field with 8+ years of programming experience preferably in processing clinical trial data in the biotechnology, ph...