- Eisai, Inc (Nutley, NJ)
- …If this is your profile, we want to hear from you. The Associate Director, Clinical Programming must have expertise in addressing technical challenges ... will be responsible for implementing new technological solutions for end users.The Associate Director, Clinical Programming manages and oversees JReview and SAS… more
- C-Clinical Dallas (Dallas, TX)
- Description Senior CRA - Dallas Area C- Clinical is hiring a Senior Clinical Research Associate (CRA) with experience in CNS, oncology, or metabolic ... site initiation visits, routine monitoring visits, close-out visits of clinical sites, and maintenance of study files,...1, a complex indication with in-patient monitoring, Or metabolic studies Or *3 years or more as a CRA… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Global Clinical Supply (GCS) organization is accountable for managing the 'end-to-end' integrated clinical supply chain across the full ... Company's Research & Development Division portfolio of clinical trial s .- GCS is accountable for the...ensures proper allocation of drug product as needed across studies within assigned program(s) . - Responsible for identifying… more
- Pharmaceutical Research Associates, Inc (New York, NY)
- Overview As a Senior Clinical Research Associate you will be joining the world's largest & most comprehensive clinical research organization, powered by ... experience. A licensed healthcare professional (eg, RN) is also acceptable. An experienced Clinical Research Associate with 5+ years of clinical monitoring… more
- Protara Therapeutics, Inc. (New York, NY)
- …to CRO CAPA development, as required. Review and contribute to CO sections of Clinical Study Reports (CSRs) in collaboration with Clinical Science team. ... needs via oral or enteral routes. Job Overview: The Clinical Trial Manager (CTM)/ Clinical Research Associate...data when an onsite visit is not feasible. Review clinical monitoring reports (Pre- Study Visits, Site Initiation… more
- Mount Sinai Hospital (New York, NY)
- …The Clinical Research Associate I monitors all aspects of clinical research trial(s) Clinical study life-cycle responsibilities including site ... clinical , Phase I through Phase IV, and post-marketing studies . Responsibilities Prepares and completes critical study ... as a clinical trial assistant or clinical research associate is highly desirable. About… more
- The Fountain Group (Alameda, CA)
- Currently seeking a Clinical Research Associate in Alameda, CA. Details for the position are as follows: Job Description: Pay: $45-50/hr. Travel: 30-50% 6-month ... Phase I-IV studies per Federal Regulations and ICH guidelines. Write study protocols, monitor site adherence, ensure timely patient enrollment, and manage CRF… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …biomarker strategy in collaboration with Translational Medicine/Clin Pharm; May act as Clinical study leader (CSL) Study Planning and Execution: Provides ... medical and/or scientific direction to Clinical Operations. Represents Clinical Development on Project Teams.Responsibilities: Study Strategy: Provides the… more
- IQVIA, Inc. (Durham, NC)
- …located. IQVIA's Cardiovascular, Renal and Metabolic (CVRM) team are looking for an Associate Clinical Project Director to work across our growing Obesity ... portfolio. Obesity experience is a must-have! Associate Clinical Project Management Directors manage and...for the strategic development and execution or delivery of clinical studies in line with agreed upon… more
- Merck & Co. (North Wales, PA)
- …field experienceDegree in life sciences, preferred.Experience in planning and executing clinical studies in ophthalmology highly preferredAs an Equal Employment ... the operational planning and execution of one or more clinical trials. In this position, you will have the...Trial Team lead. Leads and directs teams in key study planning, development, and execution elements (eg operational reviews,… more
- Regeneron Pharmaceuticals, Inc. (Tarrytown, NY)
- The Associate Manager, Clinical Drug Supply &...drug supply manager of multiple small and/or less complex clinical studies for the functional area in ... applies to internally sourced studies and/or CRO/Partnered studies . Collaborates and interacts with clinical trial...Manages supply planning and timelines to ensure alignment with study plans and timelines and overall clinical … more
- Baptist Health (Birmingham, AL)
- …fo critical healthcare equipment. At Brookwood Baptist Health Hospital the Associate Clinical Engineer Tech ensures diagnostic/therapeutic or electronics ... to support unplanned events during after-hours and weekends. Qualifications Education/Training - Associate 's degree in a technical area of study required. -… more
- Merck & Co. (North Wales, PA)
- …and medical monitoring of clinical studies .Supervises development of clinical documents including protocols, clinical study reports and background ... Job DescriptionThe Associate Vice President (AVP)/Section Head, Global Clinical Development, Pediatrics will focus on driving strategy, development, and… more
- Genmab (NJ)
- …as trial responsible statistician with responsibilities as described below. The Associate Director contributes to clinical development strategies and ... we would love to have you join us!The RoleThe Associate Director acts as a statistical expert supporting the... Director acts as a statistical expert supporting the clinical development of compounds as compound and/or indication lead… more
- Merck & Co. (Rahway, NJ)
- …and programsIn collaboration with internal teams and external partners, designs studies , authors study protocols, develops measurement questionnaires, case ... Job DescriptionRole SummaryUnder the guidance of a senior leader, an Associate Principal Scientist/ Associate Director, has primary responsibility for… more
- Nurix (San Francisco, CA)
- …and maintaining a risk based, phase appropriate audit approach and ensuring clinical studies are conducted in accordance with applicable regulatory requirements, ... a new script to outmatch disease. Responsibilities and Duties: The Senior Manager/ Associate Director of Clinical Quality Assurance Auditor is responsible for… more
- Merck & Co. (South San Francisco, CA)
- …West Point, PA / Rahway, NJ is seeking a curious and collaborative Associate Director to support our rapidly expanding cardiometabolic and ophthalmology pipelines. - ... As an Associate Director, you will represent QP2 on cr o...sci e ntis ts to discover and advance the clinical development of novel therapeutic agents for cardiometabolic and… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …programming innovation outside of DS and establish the company reputations and images.- Develop study specific shiny apps or execute shiny apps at study level. ... signaling detections and across compounds safety reviews (ie, ILD). Collaborate with Clinical Development and Clinical Sciences for effective data surveillance… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionJoin Our Team as an Associate Principal Scientist/ Associate Director in Biologics Drug Substance Commercialization!Are you ready to make a ... in and/or spearhead cross-divisional technical teams focused on late-stage clinical process development, characterization, and technology transfer of biopharmaceutical… more
- Merck & Co. (San Francisco, CA)
- Job Description Position Description: Associate Director, DSCS Digital Implementation Project ManagerWithin the Development Sciences and Clinical Supply (DSCS) ... execution and management of DSCS Digital initiatives.Development Sciences and Clinical Supply (DSCS) enables Drug Substance, Drug Product, Analytical Development,… more
