- University of Iowa Hospitals & Clinics (Iowa City, IA)
- …either a Clinical Trials Research Assistant, requisition 25004144 or Clinical Trials Research Associate , requisition 25004146, based on the ... conduct and manage the regulatory aspect of clinical trials to deliver and evaluate research ...submit application forms and serve as liaison to the Clinical Research Unit (CRU), the Pharmacy and… more
- Merck & Co. (Rahway, NJ)
- …and barriers to reimbursement and market access, and provide input into clinical , regulatory , payer/access, marketing and evidence generation strategy and ... Job DescriptionRole SummaryUnder the guidance of a senior leader, an Associate Principal Scientist/ Associate Director, has primary responsibility for… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …and Device Development and Commercialization process.Experience with developing and documenting regulatory strategies in coordination with clinical plans and ... focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders. Summary: Responsibility for… more
- Mount Sinai Hospital (New York, NY)
- Job Description The Clinical Research Associate I monitors all aspects of clinical research trial(s) Clinical study life-cycle responsibilities ... clinical reports of assigned projects for submission to regulatory authorities. Performs other duties as required. Qualifications Bachelors...studies as a clinical trial assistant or clinical research associate is highly… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders.Summary: This position manages ... working with contract manufacturing organizations CMO. This position serves as the Regulatory Affairs (RA) CMC project representative to the CMC sub team and… more
- Allen Spolden (Boston, MA)
- Job Description Responsible for providing Clinical Research support for all clinical trials. Under the direction of supervisor or designee, this position ... regulatory documents, and other administrative documents as related to clinical research functions. Initiate studies performing initiation site visits,… more
- Arrowhead Pharmaceuticals (San Diego, CA)
- …who are collaborating to bring new therapies to patients in need. The Position The Clinical Research Associate (CRA) provides support to Study Lead(s) in ... applicable regulatory requirements. Requirements: 2 years in clinical research 2 years as a ...clinical research 2 years as a Clinical Trial Associate ; study coordinator Proficient knowledge… more
- IQVIA, Inc. (Durham, NC)
- …accepted in lieu of degree. *Good knowledge of, and skill in applying, applicable clinical research regulatory requirements. *i.e., Good Clinical ... with coworkers, managers, and clients. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the… more
- Holy Cross Hospital (Fort Lauderdale, FL)
- …Purpose: This person will be responsible for the conduct of multiple Oncology clinical research activities. Ideal candidate will have industry sponsored ... be knowledgeable on and have full understanding of good clinical practices (GCP) and regulations. Will be held accountable...or other sources *FL RN License *On-Site *Oncology Experience * Research Experience What you will do: Assist in the… more
- Merck & Co. (North Wales, PA)
- … Clinical Documentation, Clinical Investigations, Clinical Judgment, Clinical Reporting, Clinical Research , Clinical Trial Documentation, ... Job DescriptionThe Associate Vice President (AVP)/Section Head, Global Clinical...research and business development priorities and prioritization of clinical assets.-May serves as the senior liaison for relevant… more
- Merck & Co. (Rahway, NJ)
- …Material(s):n/aRequired Skills:Adaptability, Adaptability, Business, Business Risks, Change Management, Clinical Development, Clinical Research , ... Supply (GCS) organization is accountable for managing the 'end-to-end' integrated clinical supply chain across the full Company's Research & Development… more
- Ochsner Health (New Orleans, LA)
- …bachelor's degree. Preferred - 2 years of experience in area of assigned clinical specialty, managing clinical research and patient databases. Certification ... clinical trials. Organizes and manages all documentation and regulatory submissions as required by the sponsor of the...Knowledge Skills and Abilities (KSAs) Knowledge of medical and clinical research terminology and processes. Ability to… more
- Krystal Biotech (Pittsburgh, PA)
- Clinical Trial Associate / Clinical Research Coordinator About Krystal Bio: At Krystal Biotech, we bring together the brightest and most eager minds to ... Job Description Summary: Krystal Biotech, Inc. is seeking a Clinical Trial Associate to support our ...periods Understanding and application of GCP, ICH, and applicable regulatory standards governing clinical research … more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …trial (small size, standard complexity in design and geographic scope). Prepares clinical section of regulatory document. Collaborates as team member with ... focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders. Summary: Oversees typically… more
- Organon (Plymouth Meeting, PA)
- …( Associate Director) is responsible for developing and implementing Regulatory Chemistry, Manufacturing & Controls (CMC) strategies for assigned small molecule ... project timelines. Preferred Experience and Skills A candidate with experience in Regulatory CMC in clinical development, initial marketing application and… more
- Velocity Clinical Research, Inc. (Annapolis, MD)
- …duties as assigned Qualifications Education/Experience: Bachelor's degree and 4 years as a Clinical Research Coordinator OR Associate 's degree and 6 years ... Overview Velocity Clinical Research is an owned and...source development review, scheduling subjects, protocol training, collection of regulatory documents, conducting visits, ensuring data is entered in… more
- CHOC - Children's Health Orange County (Orange, CA)
- …includes but is not limited to assessing feasibility of clinical research protocols, preparing materials needed for regulatory review and submission to ... Clinical research experience in a hospital setting and/or pediatric clinical research experience. Education Required: Associate degree or equivalent… more
- Duke University (Durham, NC)
- …Records participant accrual information and consent documentation for non-complex studies in clinical research management system. Uses clinical research ... area of research . Navigates processes and people involved in Duke clinical research , demonstrates the organizational awareness, and has the interpersonal… more
- Bristol-Myers Squibb Company (Princeton, NJ)
- …the Global Research organization in BMS and leads late stage clinical , pharmacological and translational research and development activities for the pipeline ... and supports late stage portfolio for regulatory , translational development and life cycle management. Translational Development drives strategy across core… more
- University of Kansas Medical Center (Kansas City, KS)
- …research (CFR, GCP, HIPAA). Experience with statutes and guidelines relevant to regulatory affairs in clinical research . Experience study budgets, ... Department: SOM KC Cancer Center Clinical Trials Administration Position Title: Clinical Research Coordinator - Cancer Center Job Family Group: Professional… more
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