Sentences with phrase «monitoring clinical research trials»

Along with my Bachelor's degree and hands - 0n experience in monitoring clinical research trials, I am confident in my ability to make a significant contribution to your organization.

Not exact matches

The Office for Human Research Protections (OHRP), an office within the Department of Health and Human Services (DHHS), develops policies to protect human subjects and monitors clinical trials at research instiResearch Protections (OHRP), an office within the Department of Health and Human Services (DHHS), develops policies to protect human subjects and monitors clinical trials at research instiresearch institutions.

For instance, clinical trial participants can avoid the inconvenience of visiting research facilities, writing down their daily activities or wearing clunky monitors.

In that older approach, trial participants worked iteratively and explicitly through target acquisition attempts while a trained clinical research technician monitored and updated the software.

«A drawback of clinical trials is that they are highly controlled and highly monitored to ensure strict adherence to protocol; however, that's not how people take drugs in the real world,» said Andrea V. Margulis, MD, ScD, senior research epidemiologist and co-author of the paper.

The Clinical Accelerator network includes approximately 80 of the world's leading physician - scientists with expertise in tumor immunology and cancer immunotherapy clinical trials, immune monitoring, and correlative rClinical Accelerator network includes approximately 80 of the world's leading physician - scientists with expertise in tumor immunology and cancer immunotherapy clinical trials, immune monitoring, and correlative rclinical trials, immune monitoring, and correlative research.

Clinical Trials Research and Billing First in Human / Early Phase PET in Oncology Case - Based Dose Reduction in Pediatric Nuclear Medicine: Practical and Necessary Radioiodine Therapy for Hyperthyroidism: The State of the Art Spondylodiscitis: Role of Imaging for Diagnosis and Monitoring Treatment Response Current Status and Future Prospects: PET and SPECT Instrumentation Alternative Payment Models and Value - Based Health Care: Nuts and Bolts Maximal Tolerated Activity of Radioactive Iodine for Metastatic Thyroid Cancer Teaching Old Radiopharmaceuticals New Tricks Intraoperative Detection Devices and Probes Molecular Imaging of Lung Inflammation Standardization of Advanced PET / SPECT Data Acquisition and Analysis Thyroid Cancer Management: Novel Therapeutics and Management Options Targeting Radionuclide Therapy in Various Non-Malignant Arthritic Conditions Using Radiosynoviorthesis (RSO) Are You Prepared for a Radiation Accident?

First, in 2001, CRI formed a partnership with the Ludwig Institute for Cancer Research to develop the Cancer Vaccine Collaborative (CVC)-- a centralized, academic, global network of clinical trial sites, immune monitoring laboratories, and clinic - grade, GMP cancer vaccine production facilities.

She gained her experience as a research investigator at The Functional Medicine Research Center (FMRC) in Gig Harbor, Washington, where she monitored patients undergoing clinical trials for insulin resistance, Type 2 Diabetes, obesity, and food alresearch investigator at The Functional Medicine Research Center (FMRC) in Gig Harbor, Washington, where she monitored patients undergoing clinical trials for insulin resistance, Type 2 Diabetes, obesity, and food alResearch Center (FMRC) in Gig Harbor, Washington, where she monitored patients undergoing clinical trials for insulin resistance, Type 2 Diabetes, obesity, and food allergies.

Clinical Research Associates can work on various stages of a clinical trial, performing tasks such as creating trial protocols, developing trial methodology, collaborating with ethics committees, liaising with doctors running the trial, making visits to the trial site, ordering supplies, monitoring expenses, and authenticating data collectioClinical Research Associates can work on various stages of a clinical trial, performing tasks such as creating trial protocols, developing trial methodology, collaborating with ethics committees, liaising with doctors running the trial, making visits to the trial site, ordering supplies, monitoring expenses, and authenticating data collectioclinical trial, performing tasks such as creating trial protocols, developing trial methodology, collaborating with ethics committees, liaising with doctors running the trial, making visits to the trial site, ordering supplies, monitoring expenses, and authenticating data collection forms.

That is why research monitors are hired to keep an eye on the research process and monitor the clinical trial results.

• Prepare protocols and case report forms to increase patient randomization • Coordinate the smooth monitoring of all trials through identification and management of qualified staff • Participate in global clinical research work and ensure that coworkers are updated of progress • Handle financial management of clinical trial programs including budget management and resource allocation • Implement training programs for staff members and handle budget control and reporting activities

Key Accomplishments • Created and implemented a clinical investigation plan which increased efficiency by 50 % • Trained 15 research assistants in handling site initiation, closeout and interim monitoring work • Introduced 8 different clinical trial committees, including clinical events committee, data safety monitoring board and steering committee • Obtained 3 informed consents for human research subjects which were in limbo for 5 years

• Maintained clinical sites and ensured compliance with Clinipace SOPs, local regulations and ICH guidelines • Developed trip reports and tracked sponsor communications • Assessed clinical trials for growth and development and coordinated efforts between Lead Clinical Research Team, Trial Manager, Monitor manager and trained monitors • Assisted with audits and generalclinical sites and ensured compliance with Clinipace SOPs, local regulations and ICH guidelines • Developed trip reports and tracked sponsor communications • Assessed clinical trials for growth and development and coordinated efforts between Lead Clinical Research Team, Trial Manager, Monitor manager and trained monitors • Assisted with audits and generalclinical trials for growth and development and coordinated efforts between Lead Clinical Research Team, Trial Manager, Monitor manager and trained monitors • Assisted with audits and generalClinical Research Team, Trial Manager, Monitor manager and trained monitors • Assisted with audits and general queries

• Seeking a Clinical Research Associate position with Piper Companies employing skills in setting up and monitoring clinical trials to ensure adherence to clinical prClinical Research Associate position with Piper Companies employing skills in setting up and monitoring clinical trials to ensure adherence to clinical prclinical trials to ensure adherence to clinical prclinical protocols.

Tags for this Online Resume: Regulatory Coordinator, Clinical Trial Management, Document managment, Quality Checking, Monitoring, Management, Data Entry, Protocol, Regulatory Affairs, Clinical Research, Compliance, Document Management, Email

Tags for this Online Resume: Monitoring, Protocol, Cardiovascular, Clinical Research, Management, Pharmaceutical, Research, Therapy, Audit, Data Management, Medical Device, CRA, CTM, Clinical Trials

Tags for this Online Resume: clinical, research, project management, biology, medical, science, monitoring, clinical trials, regulatory, quality assurance, laboratory

Summary of Qualifications Clinical Research Manager, Associate, Monitor, Coordinator, with over 25 years experience in the medical field and 21 years experience in clinical trials with extensive experience in the fields of Cardiology, Electrophysiology, Neurology, Urology, Autoimmune, Respiratory, Gastroenterology, Weight Loss, Diabetes, Women's Studies, Arthritis, COPD, Gynecology, Endocrinology, Rheumatology and StemClinical Research Manager, Associate, Monitor, Coordinator, with over 25 years experience in the medical field and 21 years experience in clinical trials with extensive experience in the fields of Cardiology, Electrophysiology, Neurology, Urology, Autoimmune, Respiratory, Gastroenterology, Weight Loss, Diabetes, Women's Studies, Arthritis, COPD, Gynecology, Endocrinology, Rheumatology and Stemclinical trials with extensive experience in the fields of Cardiology, Electrophysiology, Neurology, Urology, Autoimmune, Respiratory, Gastroenterology, Weight Loss, Diabetes, Women's Studies, Arthritis, COPD, Gynecology, Endocrinology, Rheumatology and Stem Cell...

To utilize over 15 years of research monitoring and management experience and skill sets to contribute to clinical trials

Tags for this Online Resume: Clinical Research • Data Management • Statistics • Drug Safety • Clinical Study Reports • Diabetics Interventions Budget Management • Clinical Operations • Regulatory Submission Documents • Protocol Preparation • QA / QC Clinical Study R, GCP, FDA, TPD Regulations FDA Regulations • Clinical Trial Monitoring • Nutritional Biochemistry • Diet / Exercise • Metabolic Disorders, Research, Monitoring, Benefits, Cancer, Clinical Research, Insulin, clinical, oncology, pharmaceutiClinical Research • Data Management • Statistics • Drug Safety • Clinical Study Reports • Diabetics Interventions Budget Management • Clinical Operations • Regulatory Submission Documents • Protocol Preparation • QA / QC Clinical Study R, GCP, FDA, TPD Regulations FDA Regulations • Clinical Trial Monitoring • Nutritional Biochemistry • Diet / Exercise • Metabolic Disorders, Research, Monitoring, Benefits, Cancer, Clinical Research, Insulin, clinical, oncology, pharmaceutiClinical Study Reports • Diabetics Interventions Budget Management • Clinical Operations • Regulatory Submission Documents • Protocol Preparation • QA / QC Clinical Study R, GCP, FDA, TPD Regulations FDA Regulations • Clinical Trial Monitoring • Nutritional Biochemistry • Diet / Exercise • Metabolic Disorders, Research, Monitoring, Benefits, Cancer, Clinical Research, Insulin, clinical, oncology, pharmaceutiClinical Operations • Regulatory Submission Documents • Protocol Preparation • QA / QC Clinical Study R, GCP, FDA, TPD Regulations FDA Regulations • Clinical Trial Monitoring • Nutritional Biochemistry • Diet / Exercise • Metabolic Disorders, Research, Monitoring, Benefits, Cancer, Clinical Research, Insulin, clinical, oncology, pharmaceutiClinical Study R, GCP, FDA, TPD Regulations FDA Regulations • Clinical Trial Monitoring • Nutritional Biochemistry • Diet / Exercise • Metabolic Disorders, Research, Monitoring, Benefits, Cancer, Clinical Research, Insulin, clinical, oncology, pharmaceutiClinical Trial Monitoring • Nutritional Biochemistry • Diet / Exercise • Metabolic Disorders, Research, Monitoring, Benefits, Cancer, Clinical Research, Insulin, clinical, oncology, pharmaceutiClinical Research, Insulin, clinical, oncology, pharmaceuticlinical, oncology, pharmaceutical, gcp

Oversaw and monitored trial sites for study protocol adherence and SOPs, and provided appropriate verbal and written feedback to clinical research sites.

Work History Title: Senior Clinical Research Associate Company / Location United BioSource Corporation Kansas City, MO / Regional United States Dates July 2014 - January 2015 Accountabilities Implement and monitor clinical trials for medications and devices to ensure sponsor and iClinical Research Associate Company / Location United BioSource Corporation Kansas City, MO / Regional United States Dates July 2014 - January 2015 Accountabilities Implement and monitor clinical trials for medications and devices to ensure sponsor and iclinical trials for medications and devices to ensure sponsor and invest...

Tags for this Online Resume: clinical, affairs, scientific, trials, innovative, management, summary, documents, submission, regulatory, 510 (k), ISE, ISS, PK / PD, communicating, monitoring, tactical, strategic, literature, direct, vision, Lead, Director, documentation, resources, execution, consensus, effectiveness, safety, CRA, IVD, medical, device, pharmaceutical, presentation, manuscript, abstract, poster, programs, leadership, career, development, appraisals, optimize, goals, objectives, internal, external, research, investigator, stakeholders, customers, prioritize, product, support, milestones, Microsoft, Word, Excel, statistics, data, analysis, Powerpoint, publication, growth, deliverables, diagnostic, prognostic, treatment, competitive, proven, ability, capable, assess, strategy, feasibility, methodology, design, develop, produce, recommend, recommendation, therapeutic, supervision, review, performance, appraisal, application, indication, company, collaborate, expert, justification, senior, executive, assessment, experienced, marketing, pre-market, pre-IDE, protocol, communication, utility, pharmacology, service, deliver, delivery, drug, metabolism, absorption, excretion, train, training, mentor, mentoring, CRO, reimbursement, XLSTAT, Prism, relationship, contract, consult, consultant, ownership, responsibility, authority, delegate, trends, direction, in - vitro, commercialize, commercialization, approval, clearance, patient, oncology, cancer, metabolic, cardiovascular, kidney, disease, health, outcomes, safe, effective, toxicity, novel, unique, unmet, need, advisors, advisory, committee, IRB, ethical, justified, supportive, care, associate

SUMMARY: * rn, bsn, cpm, * Over 28 years of Clinical Research experience * Respiratory, Ophthalmology, Oncology, Infectious Disease, Cardiovascular, CNS and Gastrointestinal * Phase I, II and III experiences * 14 years of Clinical Trial / Project Management experience * 4 years of field monitoring experience * 14 years of experience providing oversight to CTAs and CRAs PurDue PharmA July 2017 - present Sr Clinical Project Man...

Tags for this Online Resume: Project Management, Project Manager, Clinical Research, Research, Management, Monitoring, Protocol, Query, Acceptance Testing, Advertising, clinical, protocol, triaClinical Research, Research, Management, Monitoring, Protocol, Query, Acceptance Testing, Advertising, clinical, protocol, triaclinical, protocol, trial, phase

Tags for this Online Resume: Clinical Research, Research, Cancer, Clinical Operations, Oncology, clinical research, monitor, senior clinical research associate, clinical, phase iii, phase iv, phase ii, phase i, clinical trials, pharmaceutical, cro, reClinical Research, Research, Cancer, Clinical Operations, Oncology, clinical research, monitor, senior clinical research associate, clinical, phase iii, phase iv, phase ii, phase i, clinical trials, pharmaceutical, cro, reResearch, Research, Cancer, Clinical Operations, Oncology, clinical research, monitor, senior clinical research associate, clinical, phase iii, phase iv, phase ii, phase i, clinical trials, pharmaceutical, cro, reResearch, Cancer, Clinical Operations, Oncology, clinical research, monitor, senior clinical research associate, clinical, phase iii, phase iv, phase ii, phase i, clinical trials, pharmaceutical, cro, reClinical Operations, Oncology, clinical research, monitor, senior clinical research associate, clinical, phase iii, phase iv, phase ii, phase i, clinical trials, pharmaceutical, cro, reclinical research, monitor, senior clinical research associate, clinical, phase iii, phase iv, phase ii, phase i, clinical trials, pharmaceutical, cro, reresearch, monitor, senior clinical research associate, clinical, phase iii, phase iv, phase ii, phase i, clinical trials, pharmaceutical, cro, reclinical research associate, clinical, phase iii, phase iv, phase ii, phase i, clinical trials, pharmaceutical, cro, reresearch associate, clinical, phase iii, phase iv, phase ii, phase i, clinical trials, pharmaceutical, cro, reclinical, phase iii, phase iv, phase ii, phase i, clinical trials, pharmaceutical, cro, reclinical trials, pharmaceutical, cro, regulatory