- J&J Family of Companies (Washington, DC)
- Senior Clinical Research Associate - 2406171534W **Description** Abiomed, part of Johnson & Johnson's MedTech, is recruiting for a Senior Clinical ... activities on assigned clinical trials. The Senior Clinical Research Associate should ensure... trial/study safety, in keeping with protocols, GCP (Good Clinical Practices), PHI (Personal Health Information) and regulatory… more
- Merck (Washington, DC)
- …as primary site contact and site manager throughout all phases of a clinical research study, taking overall responsibility of allocated sites. Actively develops ... and expands the territory for clinical research , finding and developing new sites....a timely manner. + Collects, reviews, and monitors required regulatory documentation for study start-up, study maintenance and study… more
- Novo Nordisk (Washington, DC)
- …a difference? The Position Drives the understanding and delivery of quality clinical research (patient safety, rights and wellbeing; data reliability; scientific ... About the Department The Clinical , Medical and Regulatory (CMR) department...and improvement/innovation projects for NACD and Novo Nordisk (eg, clinical trial site staff, clinical research… more
- Kelly Services (Washington, DC)
- …take the next step in your career, trust The Experts at Hiring Experts. The Sr. Clinical Research Associate is responsible for in the execution of ... a Sub-Investigator for a fulltime, direct-hire position with a research site in Tampa, FL. If you're passionate about...plan, case report forms, etc.). + Remain current on clinical trial regulatory requirements and guidelines (eg… more
- Guidehouse (Bethesda, MD)
- … Research Coordinator (CCRC), or Certified Clinical Research Associate (CCRA) + Liaising with regulatory authorities + Training clinical trial ... The primary role for this Protocol Navigator (PN) position is to provide clinical research regulatory support through the NINDS Clinical Trials Unit… more
- Guidehouse (Bethesda, MD)
- … Research Coordinator (CCRC), or Certified Clinical Research Associate (CCRA) + Liaising with regulatory authorities + Training clinical trial ... The primary role for this Protocol Navigator (PN) position is to provide clinical research regulatory support through the NINDS Clinical Trials Unit… more
- Georgetown Univerisity (Washington, DC)
- …inquiry and making a difference in the world. Requirements Job Overview The Clinical Research Coordinator 2 (CRC2) is responsible for managing and coordinating ... adhere to the university requirements for the conduct of clinical research . Additional job requirements include, but...a daily basis, the CRC2 will report to the Associate Director of Clinical Trials. The CRC2… more
- Georgetown Univerisity (Washington, DC)
- …confidentiality, and adhere to university standards for clinical research conduct. Responsibilities also include regulatory maintenance, compliance with ... inquiry and making a difference in the world. Requirements Clinical Research Coordinator 2, Department of Neurology...On a daily basis, the CRC2 reports to the Associate Director of Clinical Trials, and is… more
- Amgen (Washington, DC)
- …of clinical research experience Or Bachelor's degree and 6 years of clinical research experience Or Associate 's degree and 10 years of clinical ... time for a career you can be proud of. Clinical Research Senior Medical Scientist **Live** **What...FDA and EMEA/CHMP regulations and guidelines, and applicable international regulatory requirements + Experience authoring clinical sections… more
- Amgen (Washington, DC)
- …million patients worldwide. It's time for a career you can be proud of. ** Clinical Research Sr Medical Scientist, Endocrinology** **Live** **What you will do** ... commercial input into the development program. Participate and provide clinical input into safety and regulatory interactions.... Clinical Scientists or GDL and identify new clinical research opportunities. **Win** **What we expect… more
- Alaka'ina Foundation Family of Companies (Silver Spring, MD)
- …(GCP) and Human Subjects Protection (HSP) DESIRED SKILLS AND EXPERIENCE: + Certified Clinical Research Associate (CCRA) + DoD experience REQUIRED CITIZENSHIP ... REQUIRED SKILLS AND EXPERIENCE: + Knowledge and experience in the areas of clinical research and regulatory affairs as related to clinical studies,… more
- Merck (Washington, DC)
- …**Required Experience and Skills:** + Minimum of 6 years of relevant experience in clinical research , including at least 2 years of direct experience with ... colleagues, GCTO Country Operations, other GCTO functional areas, Pharmacovigilance (PV), Global Regulatory Affairs and Clinical Safety (GRACS), IT, etc.) is… more
- Amgen (Washington, DC)
- … Research . With a constantly growing demand for information from regulatory and reimbursement agencies, Observational Research (OR) is a critical ... inform regulatory decision making (eg, label expansion/change) and fulfill regulatory requirements across the globe. + Managing research projects involving… more
- Amgen (Washington, DC)
- …functionally aligned teams. With a constantly growing demand for information from regulatory and reimbursement agencies, Observational Research (OR) has become a ... regarding the frequency and distribution of disease or the clinical burden of disease, the natural history or ...experience Or Bachelor's degree and 5 years of related research and scientific experience Or Associate 's degree… more
- Medtronic (Washington, DC)
- …procedures including TMVR or LAAC or other adjacent therapies + Clinical Research experience including coordinating multi-center trials and/or significant ... group presentations and hands-on experience with interventional/surgical cardiac procedures + Clinical Research experience in structural heart or other medical… more
- IQVIA (Falls Church, VA)
- …(~20%) IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in ... Associate Director, Digital Measures, Patient Centered Solutions (PCS)...includes qualitative (eg, patient interviews, focus groups), quantitative (eg, clinical outcome assessments (COAs)/patient-reported outcomes (PROs), preference research… more
- Sumitomo Pharma (Washington, DC)
- …and suppliers of drug substances and drug products used for investigational clinical trials and/or commercial phases. The Associate Director ensures compliance ... ** Associate Director, GMP Quality Control** Sumitomo Pharma America...and communicate changes to contract manufacturing organizations, testing laboratories, clinical sites and regulatory affairs as needed.… more
- Merck (Washington, DC)
- …development (MIDD) to routinely enable efficient drug discovery/development and/or regulatory decisions. The Pharmacometrics group within QP2 brings an experienced ... of decision-making at ouor company, this position offers an opportunity for the Associate Director to drive pipeline impact across therapy areas. This Associate … more
- Charles River Laboratories (Rockville, MD)
- Senior Biomanufacturing Associate - Upstream & Compliance Req ID #: 222027 Location: Rockville, MD, US, 20850 For 75 years, Charles River employees have worked ... can feel passionate about. **Job Summary** The Senior Biomanufacturing Associate - Upstream & Compliance will report to the...With more than 50 years of experience and proven regulatory expertise, the Charles River Biologics group can address… more
- Charles River Laboratories (Rockville, MD)
- QC Associate I - Environmental Monitoring - 4 - 10 hour shifts, Thursday - Sunday from 8am - 6pm 1 Req ID #: 222840 Location: Rockville, MD, US, 20850 For 75 years, ... our growing business in the CMO industry. The QC Associate I - Environmental Monitoring will perform microbiological testing,...With more than 50 years of experience and proven regulatory expertise, the Charles River Biologics group can address… more