Sentences with phrase «research protocol compliance»

Practice plus, Irving, TX May 2007 — July 2010 Clinical Research Intern • Oversaw and implemented daily operational aspects of clinical research • Worked closely with clinical trial sponsors for site assessment, qualification and initiation visits • Ensured research protocol compliance while subjects were at work

Not exact matches

Analyzing data on 4,157 caregivers working at 35 different hospitals, the research team behind the results examined the relationship between busyness - induced exhaustion and compliance with standard hand - washing protocols.

The emotion - processing cannabis study was approved by CSU's Office of Research Integrity and Compliance Review Office Institutional Review Board (Protocol ID: 12 - 3716H).

Trained, monitored, and supervised research - naïve sites to ensure protocol compliance and adherence to GCP principles as part of a multi-centered dental practice - based research network &

Duties shown on sample resumes of Research Nurses include administering tests, collecting and processing lab specimens, and performing investigational drug accountability in compliance with research prResearch Nurses include administering tests, collecting and processing lab specimens, and performing investigational drug accountability in compliance with research prresearch protocols.

2014 - present • Oversee entire recruitment process: finding and screening potentially suitable subjects for relevant studies, and ensuring proper protocol for obtaining and documenting consent is followed through • Communicate and collaborate with laboratories and investigators on findings, and report on clinical research results • Conduct and monitor studies to ensure proper procedures are carried through in compliance with company policies and federal and state regulations • Counsel health care professionals on proper treatment and dosages • Manage all researchers and acquire necessary space and equipment to conduct studies

Liaison between principal investigators (PIs) and sponsors, and researched personnel regarding status of submitted protocols, and created and updated protocol files (i.e. approval letters, consent forms, and documents for regulatory and compliance).

Main Responsibilities: Site management to ensure proper adherence to protocol Work on Phase I - IV clinical research studies and various therapeutic areas Identify, select, initiate and close - out appropriate investigational sites Ensure compliance to the study protocol, Standard Operating Procedures, applicable regulations, and the principles of...

Lead Mechanical Engineer — Holwall Products Assemblage — Fayetteville, TN — 2012 — 2015 • Supervise design, development, and assessment of tools, components, and mechanical equipment • Meet with supervisors and team leaders to review product specifications • Collaborate on installation, operations, and maintenance of equipment throughout plant • Improve workforce optimization, including space requirements and equipment layouts • Reinforce compliance with maintenance procedures to protect safety of personnel and equipment • Implement process procedures, including maintenance schedules and testing protocols Mechanical Designer — UGW Elements — Elkmont, AL — 2013 — Present • Assess project requirements and ensure compliance with specifications • Measure and improve performance of mechanical devices and components • Maintain equipment to ensure safety, efficiency, and reliability • Produce designs and testing protocols • Provide technical advice to personnel from utilities companies, representatives from government agencies, and research organizations

Researched and wrote spa menu and manual including all service protocols and compliance standards for all local health regulations.

• Enhanced the accuracy of visual diagnostic assessment process up till 97 % by implementing modern, computerized and research based evaluative protocols • Reduced annual procurement cost by $ 30K by recommending less costly, reliable replacements of conventional and expensive visual assessment equipment • Brought the hospital's optometric department in 100 % compliance with HIPPA guidelines • Conducted numerous educational workshops to spread awareness regarding safe and healthy measures and life style adaptations to prevent loss of vision among patients at risk

• A Clinical Research Coordinator position with Care ID where I may use my skills in investigational products by ensuring protocol compliance at all times.

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: Compliance, Radiation, Training, Clinical Research, Infrastructure, Monitoring, Prime, Protocol, Research, Scheduling

Morristown Memorial Hospital, Morristown • NJ 2002 — 2006 Regulatory Compliance Associate for Atlantic Health System (AHS) / Data Manager / Research Coordinator Developed and maintained Access 2003 Protocol Activity Database for Atlantic Health Systems documentation for the Institutional Review Board.

Handled all salary and non-salary expenditures and worked closely with the Research Administration Office to collaborate in pre and post award activities and ensured compliance requirements such as IACUC and IBC protocols.

Skills such as understanding consumer / physician concerns, pharmacology, clinical paper, sales management, protocol, research, compliance, ICH / GCP, follow up, ability to grasp technical data and medical terminology are tools I possess to facilitate success in this industry.

Tags for this Online Resume: Clinical Research, Communication Skills, Compliance, Management, Nursing, Pulmonary, Research, Business Plan, Needs Assessment, Protocol

Dayton Outpatient Center and Research (Dayton, OH) 8/2007 — 4/2008 Research Assistant Principal Investigator — Dr. Suresh Gupta; Sub Investigators — Dr. Arora, Dr. Choi Research Coordinator — Ritu Singla • Aided with the development and execution of various clinical research studies and programs, with a focus in diabetic neuropathy, rheumatoid arthritis, osteoarthritis, CRPS, and NSAID - induced gastric ulcers • Worked under specific instructions to run routine tests, experiments, and procedures, ensuring compliance with all established policies, procedures, quality control objectives, and related safety, environmental, and infection control standards • Collaborated in the compilation and verifications of research data, samples, and specimens while participating in related data entry, analysis, and interpretation utilizing various data management and analysis programs • Performed routine data verification and quality control, ensuring data integrity and compliance with prescribed study protocol • Searched related literature and information sources for relevant information pertaining to experiments and procedures • Assisted in the setup, operation, and maintenance of all research equipment and instruments • Administered various logistical, scheduling, and office management functions to provide high - quality subject service, efficient file and data organization, and effective department opResearch (Dayton, OH) 8/2007 — 4/2008 Research Assistant Principal Investigator — Dr. Suresh Gupta; Sub Investigators — Dr. Arora, Dr. Choi Research Coordinator — Ritu Singla • Aided with the development and execution of various clinical research studies and programs, with a focus in diabetic neuropathy, rheumatoid arthritis, osteoarthritis, CRPS, and NSAID - induced gastric ulcers • Worked under specific instructions to run routine tests, experiments, and procedures, ensuring compliance with all established policies, procedures, quality control objectives, and related safety, environmental, and infection control standards • Collaborated in the compilation and verifications of research data, samples, and specimens while participating in related data entry, analysis, and interpretation utilizing various data management and analysis programs • Performed routine data verification and quality control, ensuring data integrity and compliance with prescribed study protocol • Searched related literature and information sources for relevant information pertaining to experiments and procedures • Assisted in the setup, operation, and maintenance of all research equipment and instruments • Administered various logistical, scheduling, and office management functions to provide high - quality subject service, efficient file and data organization, and effective department opResearch Assistant Principal Investigator — Dr. Suresh Gupta; Sub Investigators — Dr. Arora, Dr. Choi Research Coordinator — Ritu Singla • Aided with the development and execution of various clinical research studies and programs, with a focus in diabetic neuropathy, rheumatoid arthritis, osteoarthritis, CRPS, and NSAID - induced gastric ulcers • Worked under specific instructions to run routine tests, experiments, and procedures, ensuring compliance with all established policies, procedures, quality control objectives, and related safety, environmental, and infection control standards • Collaborated in the compilation and verifications of research data, samples, and specimens while participating in related data entry, analysis, and interpretation utilizing various data management and analysis programs • Performed routine data verification and quality control, ensuring data integrity and compliance with prescribed study protocol • Searched related literature and information sources for relevant information pertaining to experiments and procedures • Assisted in the setup, operation, and maintenance of all research equipment and instruments • Administered various logistical, scheduling, and office management functions to provide high - quality subject service, efficient file and data organization, and effective department opResearch Coordinator — Ritu Singla • Aided with the development and execution of various clinical research studies and programs, with a focus in diabetic neuropathy, rheumatoid arthritis, osteoarthritis, CRPS, and NSAID - induced gastric ulcers • Worked under specific instructions to run routine tests, experiments, and procedures, ensuring compliance with all established policies, procedures, quality control objectives, and related safety, environmental, and infection control standards • Collaborated in the compilation and verifications of research data, samples, and specimens while participating in related data entry, analysis, and interpretation utilizing various data management and analysis programs • Performed routine data verification and quality control, ensuring data integrity and compliance with prescribed study protocol • Searched related literature and information sources for relevant information pertaining to experiments and procedures • Assisted in the setup, operation, and maintenance of all research equipment and instruments • Administered various logistical, scheduling, and office management functions to provide high - quality subject service, efficient file and data organization, and effective department opresearch studies and programs, with a focus in diabetic neuropathy, rheumatoid arthritis, osteoarthritis, CRPS, and NSAID - induced gastric ulcers • Worked under specific instructions to run routine tests, experiments, and procedures, ensuring compliance with all established policies, procedures, quality control objectives, and related safety, environmental, and infection control standards • Collaborated in the compilation and verifications of research data, samples, and specimens while participating in related data entry, analysis, and interpretation utilizing various data management and analysis programs • Performed routine data verification and quality control, ensuring data integrity and compliance with prescribed study protocol • Searched related literature and information sources for relevant information pertaining to experiments and procedures • Assisted in the setup, operation, and maintenance of all research equipment and instruments • Administered various logistical, scheduling, and office management functions to provide high - quality subject service, efficient file and data organization, and effective department opresearch data, samples, and specimens while participating in related data entry, analysis, and interpretation utilizing various data management and analysis programs • Performed routine data verification and quality control, ensuring data integrity and compliance with prescribed study protocol • Searched related literature and information sources for relevant information pertaining to experiments and procedures • Assisted in the setup, operation, and maintenance of all research equipment and instruments • Administered various logistical, scheduling, and office management functions to provide high - quality subject service, efficient file and data organization, and effective department opresearch equipment and instruments • Administered various logistical, scheduling, and office management functions to provide high - quality subject service, efficient file and data organization, and effective department operations

If you need to do research, or to run your program in strict compliance with the protocol, this packet is for you.