Healthcare and Safety Management jobs in the Biotech, R&D, Science category

Job ID: 742 Position Description: The Associate Director manages and leads projects, people, and processes on behalf of Global Drug Safety (GDS), Operations. The Associate Director is involved with corporate and departmental level initiatives and special projects with a greater business impact, typically focused on identifying areas for continuous improvement and facilitating the design/redesign a...
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TechData is looking for Outcome research statistician, Biostatistician (some can be telecommuting), SAS Programmer/Statistical Programmer (Some can be telecommuting), Sr. Clinical Data Manager, Drug Safety Specialist, Medical Writers for our pharmaceutical clients in Central NJ. Please see below requirements and send your resume to: dan.chen@techdataservice.com or recruiting@techdataservice.com. T...
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PATIENT SAFETY DATA SPECIALIST REQUIREMENT #13-00488 RECRUITER: CINDI PISNOY JOB LOCATION: WILMINGTON, DE MAY 28, 2013 W-2 CANDIDATES ONLY!! Project Description: Qualified to degree level in biosciences or an appropriate healthcare or pharmaceutical industry background Experience if possible authoring, negotiating and managing safety data exchange agreements with business partners, vendor manageme...
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Yoh has a long term contract opportunity for a Clinical Safety Associate I to join our client, a world leader in the pharmaceutical industry, located in San Francisco, CA. Job Responsibilities: - Performs a review of ancillary documentation accompanying ICSR reports and identifies pertinent clinical information for incorporation into the case narrative. - Performs Data Capture and Quality Review f...
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TechData is looking for Validation Analyst (6 positions), Sr. Drug Safety Associate, SAS Programmer (Some can be telecommuting), Biostatistician (Telecommuting), Sr. Clinical Data Manager for our pharmaceutical clients in SFC, CA. Please see below requirements and send your resume to: dan.chen@techdataservice.com or recruiting@techdataservice.com. TechData offers very competitive pay rate and bene...
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Why Work at PAREXEL: PAREXEL International Corporation is a leading global bio/pharmaceutical services organization, providing a broad range of knowledge-based contract research, consulting, and medical communications services to the worldwide pharmaceutical, biotechnology and medical device industries. Committed to providing solutions that expedite time-to-market and peak-market penetration, PARE...
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Why Work at PAREXEL: PAREXEL International Corporation is a leading global bio/pharmaceutical services organization, providing a broad range of knowledge-based contract research, consulting, and medical communications services to the worldwide pharmaceutical, biotechnology and medical device industries. Committed to providing solutions that expedite time-to-market and peak-market penetration, PARE...
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A health care company with global reach. A product pipeline filled to the brim. A team committed to scientific advancement. Think what's possible. A global healthcare leader, Novartis has one of the most exciting product pipelines in the industry today. A pipeline of innovative medicines brought to life by diverse, talented, performance driven people. All of which makes us one of the most rewardin...
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Medical Director, Drug Safety: Exciting & Growing Top 20 Biopharma Co., NJ Summary: Our client has a new opening for a Medical Director, Drug Safety who will be responsible for leading the pharmacovigilance strategies for various compounds in development. This person will utilize their drug safety and clinical development experience to ensure effective collaboration across development teams. This ...
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Medical Director Drug Safety & Pharmacovigilance, Oncology: Top 20 Global Pharma Co., Northern NJ Our client is a growing, stable, multi-billion dollar global pharmaceutical company with marketed products in various therapeutic areas. They are looking to hire an experienced Medical Director, Drug Safety to be a key person in leading safety Risk Management Processes, safety assessment activities, i...
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Company: Siemens Medical Solutions USA, Inc. Division: SMS - Molecular Imaging Location: FL - Tampa Req ID: 123236 Position Title: Chemist Experience Level: Entry Level Education Required: Bachelors Degree or equivalent experience Travel Required: Yes Company Description: Siemens’ Healthcare Sector is one of the world's largest suppliers to the healthcare industry and a leader in medical imaging, ...
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Position Description: We are currently seeking a Scientific Affairs Sr. Specialist who will support the successful execution of a protocol using strong management and organizational skills. The Scientific Affairs Sr. Specialist assists both Scientific Affairs and Regulatory Affairs teams to address and manage obstacles and ensure projects are completed with quality in a timely manner. This positio...
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We're Grifols Plasma Operations, a division of Grifols, S.A., a $3 billion plasma manufacturer headquartered in Barcelona, Spain. Founded in 1940 with 11,000 employees worldwide, we're the largest manufacturer of plasma-derived therapies in Europe and the third largest in the United States. We serve healthcare professionals and patients in over 90 countries, have an unmatched record of product saf...
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Position Description: We are currently seeking an Associate Director of Clinical Affairs is responsible, in collaboration with the clinical Research Project Managers, for development and execution of the clinical research studies. The Associate Director will act in a supervisory capacity to the clinical Research Project Managers but will be jointly responsible for the delivery of timely trials wit...
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Johnson & Johnson companies are equal opportunity employers. Senior Clinical Scientist (Medical Affairs & Clinical Research)-9044130530 Description Johnson & Johnson Consumer Products Company, a member of Johnson & Johnson&'s Family of Companies, is recruiting a Senior Clinical Scientist (Medical Affairs & Clinical Research) to be located in either Fort Washington, PA or Skillman, NJ. The Senior C...
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Role Centre of Excellence (CoE) Medical Writing Lead Role Description The Medical Writing Lead will be accountable to set the Centre of Excellence (CoE) for Medical Writing (MW) to build capability and capacity for the MW deliveries, ensure quality of service delivery and meeting client SLAs and KPIs by becoming a successful interface between the Cognizant team (MWs) and internal (Account Managers...
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Responsibilities: Review the Triage incoming reports for initial assessment of seriousness, expectedness, causality, and reportability for reports from clinical trials and post marking sources in accordance with local work instructions, US FDA regulations, and international guidelines and regulations with high level of accuracy, accountability, and minimal supervision Assist with data entry of inc...
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Lantheus Medical Imaging is a global leader in developing, manufacturing and distributing innovative diagnostic imaging agents. For more than 55 years, Lantheus has been dedicated to creating and providing pioneering medical imaging solutions to improve the treatment of human disease. The companys proven success in discovering, developing and commercializing innovative medical imaging agents provi...
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Position Description: We are currently seeking a Corporate VP of Clinical Affairs, who would be responsible for developing and executing clinical trial strategies as well as oversight of all drug/device US clinical studies. The position is also responsible for the strategic planning phase through conducting and reporting of the trial results. This will include design and implementation of protocol...
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(3 shift operation) JHP Pharmaceuticals, located in Rochester, Michigan, is an integrated specialty healthcare company that specializes in sterile injectable products. JHP manufactures and sells brand aseptic injectable pharmaceuticals in hospital and clinical settings and provides contract manufacturing services for global pharmaceutical companies. JHP's own product portfolio includes leading dia...
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Johnson & Johnson companies are equal opportunity employers. QA SCIENTIST III Lab Instrument/Equipment Qualification (1 of 2)-0213130610 Description McNeil Healthcare LLC, a member of Johnson & Johnson&'s Family of Companies, is recruiting a QA Scientist III Lab Instrument/Equipment Qualification, located in Fort Washington, Pennsylvania. McNeil Consumer Healthcare Division of McNEIL-PPC, Inc mark...
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Position Description: We are currently seeking a Director for Product Innovation who will lead team in ideation of creative pharmaceutical/drug delivery product concepts that meet strategic business opportunities. 1. Focus on market trends, end-user processes and business strategies that can be converted into new or enriched innovative product concepts or systems. 2. Research new and evolving tech...
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Requisition ID 14488BR Title Regional Clinical Research Associate (CRA)- Hartford, CT Job Category Clinical Job Description PURPOSE: Responsible for performing study activities regarding the implementation, monitoring and summarization of clinical trials to ensure patient safety and adherence to protocols, Good Clinical Practice (GCP), ICH Guidelines, federal regulations and SOPs. Close collaborat...
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Requisition ID 14486BR Title Regional Clinical Research Associate (CRA)- Jacksonville, FL Job Category Clinical Job Description PURPOSE: Responsible for performing study activities regarding the implementation, monitoring and summarization of clinical trials to ensure patient safety and adherence to protocols, Good Clinical Practice (GCP), ICH Guidelines, federal regulations and SOPs. Close collab...
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Requisition ID 14513BR Title Regional Clinical Research Associate (CRA)- Boston, MA Job Category Clinical Job Description PURPOSE: Responsible for performing study activities regarding the implementation, monitoring and summarization of clinical trials to ensure patient safety and adherence to protocols, Good Clinical Practice (GCP), ICH Guidelines, federal regulations and SOPs. Close collaboratio...
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