Clinical Trials Associate. Donate to a Team Member Join This Team. Our team of clinical operations recruitment experts were able to use our extensive network of talent to help our partner find suitable candidates. Administered clinical operations and prepared staff schedule. Learn about interview questions and interview process for 2 companies. Fundraising Progress $257.55. Self-directed Director of Clinical Operation with adaptability to meet changing operational needs. Why We Walk Warning Signs. As a member of the Leadership Team, she provides oversight of clinical operations, as well as quality and regulatory compliance for hospice and palliative care programs. Clinical operations is a highly important part of the drug development process and encompasses the whole clinical trial process from phases I-IV. Leverage your professional network, and get hired. Maintain a collaborative relationship with Clinical Team and Managers. Cary joined Hospice Buffalo in 1997, working in a variety of clinical and leadership roles throughout the organization. The Clinical and Operations Team Manager's primary responsibilities include: Leadership for the clinical and rehabilitative components of a Specialized Residential Treatment Program. The Operations Manager - RN is responsible for the day-to-day practice operations, continuity and efficiency of clinical operations, appropriate staff management, compliance to internal and … From start-up to close-out, our highly skilled clinical operations teams ensure proper planning, conduct, patient safety, and data quality, while fostering good communication between study sites and sponsors. Clinical Operations Advisory Council (COAC) At the heart of the Clinical Operations Division is the Clinical Operations Advisory Council (COAC), an interdisciplinary team of clinicians from the state hospitals who are devoted to the quality of clinical care and therapeutic services we provide. Today’s top 556 Clinical Operations Team Leader jobs in London Area, United Kingdom. Recruiter UNIVERSITY OF PENNSYLVANIA. Risk Based Monitoring . Apply to Clinical Lead Nurse, Clinic Manager, Operations Associate and more! Study Design and Management in Increasingly Complex Clinical Trials. Dokumeds Clinical Operations Team has more than 40% of Members with an MD/PhD. Extensive experience with postoperative pain models, as well as multi-therapeutic indications, specializing in mitigating placebo response, Managed and participated in the clinical research of more than 225 Phase I, early- and late-phase trials in various therapeutic areas, including the following postoperative pain indications: abdominoplasty, third molar extraction, bunionectomy, and total knee replacement, Developed and manages ERG’s Postoperative Analgesic Program across multiple clinical trial sites, Responsible for the design and build-out of a 10,000-square-foot acute pain research facility, which includes two operating rooms and 24 beds, Holds a degree from Utah Valley State College (ADN, Registered Nurse), ACRP Certification and NIH Certification, Previously managed centralized patient recruitment and retention, enrolling trials at over 20 sites, Has served in a variety of media and marketing positions at an advertising agency, TV station and apparel company, Holds a BS, Communications/Marketing from the University of Illinois at Urbana-Champaign, Sought-after operational leader in early-phase execution and study design for healthy volunteer trials, Industry expert in the management and operation of 100s of Phase I-IV clinical trials, Extensive career as a study coordinator, project manager, Director of Clinical Operations, Chief Compliance Officer and Vice President of Clinical Operations, Coauthored numerous articles pertaining to clinical pharmacology, Holds a BS, Nursing from Florida International University, Involved in all aspects of study conduct for more than 1800 clinical trials with a focus on Phase I studies, Cofounder of Clinical Pharmacology Associates and Clinical Pharmacology of Miami, Cofounded NPRC with the late Dr. Frederick Schaerf; manages all daily operations, Sub-Investigator, clinical research coordinator, and/or rater on more than 90 CNS trials, Frequent lecturer for both healthcare professional and community groups, Holds degrees from the University of South Florida (MS, Nursing) and the University of North Florida (BA), Conducted 100s of clinical trials in sleep disorders, dementia, Alzheimer’s disease, and other indications, Runs clinical and business operations at sites in both San Diego, CA and Rancho Bernardo, CA, Frequent contributor to study design and execution of clinical trials in Alzheimer’s disease and sleep disorders, Industry leader in clinical trial site operations and day-to-day site management, Participated in more that 150 clinical trials in various therapeutic areas including psychiatry, pediatrics and pain, Frequently engaged to serve on advisory boards by sponsors working on programs addressing chronic mental illness, Holds a degree from the University of South Florida (BS), Conducted 260 clinical trials in Phase I-IV with challenging populations in schizophrenia, major depressive disorder, bipolar disorder, post-traumatic stress disorder, essential tremor, obsessive compulsive disorder, postoperative pain, vaccine, as well as medical indications, Prior experience as a clinical research director as well as certified clinical research coordinator, Has participated in numerous late-phase clinical trials in CNS, with a focus on Alzheimer’s disease, Manages clinical and business operations at clinical trial sites in Delray Beach, FL and Stuart, FL, Holds degrees from Nova Southeastern University (MS, Mental Health Counseling) and Florida Atlantic University (BA), Has participated in more than 60 early and late-phase clinical trials, Extensive experience as a clinical research coordinator, administrator and site manager, Manages clinical and business operations for Endeavor Clinical Trials, Previously served as Director of Quality Assurance, Manages day-to-day clinical and business operations at Woodland Research Network, Serves as clinical team lead for Phase I and later-phase clinical research trials, Previously held positions as Project Supervisor for outpatient studies and Charge Coordinator at PRA Health Sciences, Managed over 100 trials in various therapeutic areas, including neurology, psychiatry, endocrinology, cardiovascular, dermatology, pain disorder, respiratory, hepatic impairment, and infectious disease, Significant experience in Phase I-IV clinical operations, project management, client services, quality assurance and data management, Holds degrees from Hunter College (MPH, Public Health) and New York University (BA, Psychology), Responsible for all clinical operations across the ERG portfolio, working closely with the medical and operational teams and bridging communication with the corporate leaders in finance, business development, and human capital, Industry veteran who oversaw clinical operations at several large multi-site SMOs, Has worked on more than 100 early- to late-phase clinical trials, Provided clinical operations and project management services to Thievon-Wright and has been with ERG since its inception, Holds a degree from the University of North Carolina (BA, Psychology), Has helped execute more than 250 clinical trials, Previously worked as the Chief Executive Officer for Research Centers of America, Experience overseeing divisions including Early and Late Phase Clinical Trial Implementation and Execution, Business Development, Quality Assurance/Control, Regulatory, Data Management, Marketing, Recruitment, Pharmacy and Laboratory Services, Received her Master’s degree in Clinical Research Organization and Management from Drexel University School of Medicine; BS in Biology from Denison University. 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