- 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
- 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
- Nurix (San Francisco, CA)
- …chapter with a new script to outmatch disease. Responsibilities and Duties: The Senior Manager/ Associate Director of Clinical Quality Assurance Auditor is ... a risk based, phase appropriate audit approach and ensuring clinical studies are conducted in accordance with...senior management, as appropriate Act as the lead Clinical Quality assurance point of contact with internal organizations… more
- Merck & Co. (Rahway, NJ)
- …effectively communicate with stakeholders at various levels, including cross-functional teams, senior management, external vendors, and clinical sites. Strong ... Job DescriptionThe Global Clinical Supply (GCS) organization is accountable for managing...ensures proper allocation of drug product as needed across studies within assigned program(s) . - Responsible for identifying… 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...of assets within the pediatric section of the Vaccine Clinical Development TA.May serve as a senior … more
- 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
- Merck & Co. (Rahway, NJ)
- Job DescriptionRole SummaryUnder the guidance of a senior leader, an Associate Principal Scientist/ Associate Director, has primary responsibility for ... and programsIn collaboration with internal teams and external partners, designs studies , authors study protocols, develops measurement questionnaires, case… 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
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …projects.At the time of implementation of a CDx study /IVDR performance evaluation study integration of an assay into clinical testing (before testing) and ... to external diagnostic business partners specifically:Use of CTA/CDx within clinical trialsDevice protocols and SAPsDevice non-significant/significant risk determinations (both… more
- Merck & Co. (North Wales, PA)
- …with senior cross-functional leadership to optimize efficiencies in the clinical development space. Preferred skills include experience in the application of AI, ... and vaccines for the benefit of patients and global human health.The Associate Vice President (AVP), Late Development Statistics, BARDS, is responsible and… 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
- Volastra Therapeutics (New York, NY)
- …for more information. JOB DESCRIPTION The Development Project Manager, Oncology ( Senior Manager/ Associate Director) will report to the Chief Medical ... COMPANY Volastra Therapeutics, Inc. is a clinical -stage oncology biotech company based in New York...funding, Volastra has established partnerships with oncology leaders. Our senior leadership team is highly experienced, supported by a… more
- Cytokinetics (South San Francisco, CA)
- …apply your deep toxicology knowledge and industry experience to design and manage non- clinical safety studies , provide strategic input to project teams, and ... to make a positive impact. Job purpose As the Associate Director of Toxicology, you will play a critical...senior management to inform key program decisions and clinical /regulatory strategies Oversee contracts, budgets and CRO relationships for… more
- Axogen (Tampa, FL)
- …Minimum 4 years' GCP auditing experience required; GCP Auditor Certification is an asset Clinical Study Management or monitoring experience is an asset GLP or ... Quality Assurance Specialist The specific duties of the Sr. Clinical Quality Assurance Associate include but are...senior QA management Create and revise of GCP-compliant Clinical Research SOPs Develop and provide routine and as… more
- CW Bill Young Department of Veterans Affairs Medical Center (Bay Pines, FL)
- …developmental, and acquired conditions of the spine and extremities. Providing clinical responsibilities that include ordering diagnostic studies and ... establishing a treatment plan based on interview, clinical findings, and study results. Demonstrating knowledge...following requirements to qualify for a specific grade level: Associate Grade : None beyond the basic requirements. Full… more
- DermBiont (Emeryville, CA)
- … data. Define and manage phase appropriate QA activities in support of preclinical studies and clinical trials. Audit and review clinical trial documents, ... Organization: DermBiont is a clinical stage biotech company with multiple active INDs...all regulatory requirements. This position will report to the Senior VP of Development. Qualifications: Have at minimum a… more
- University of California, Los Angeles (Los Angeles, CA)
- …of Psychiatry and Biobehavioral Sciences seeks a Geriatric Psychiatrist mid to senior level researcher with a focus on Alzheimer's Disease and related dementias. ... and memory research. A record of excellence in translating research findings into clinical practice is desired. A track record of mentorship of junior faculty and… more
- University of Colorado (Aurora, CO)
- …Department: CU Anschutz Police Job Title: Chief of Police and Security Operations, Associate Vice Chancellor Pos ition #: 00623412 - Requisition #: 37199 Executive ... Summary: The Chief of Police and Associate Vice Chancellor for Security Operations (AVC) serves as...public safety staff. Serve as a key advisor to senior leadership regarding issues of campus safety, crime prevention,… more
- Harmony Senior Services (Douglasville, GA)
- …The Harmony Square Director (HSD) is responsible for overseeing the non- clinical compliance within all community standards and state regulations. The HSD ... and ongoing training of Harmony Square team members in accordance with associate training standards and regulatory guidelines. Supervise and direct Harmony Square… more
- Tufts Medicine (Lowell, MA)
- …and day to day direction will be provided from the Tufts Medical Center Associate Chief Medical Officer for Quality, the Melrose Wakefield Hospital Senior ... continuing education and training of staff, quality improvement initiatives, and clinical outcome evaluation and monitoring. Work Location: Onsite Lowell General… more
