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Clinical Research Regulatory Coordinator Jobs

Clinical Research Coordinator Jobs
By Columbia University At , New York $63,000 - $65,000 a year
Bachelor's degree or equivalent in education and experience, plus two years of related experience.
Participates in patient education, obtaining informed consent, ordering pre-randomization tests and dispensing and ordering study drug.
Excellent verbal and written communications skills and attention to detail required.
Computer skills (Microsoft Office suite) required. Must be able to work independently and must strictly adhere to deadlines and protocols.
Good Clinical Practices (GCP) and HIPAA certification required.
Job Type: Officer of Administration
Research Regulatory Specialist Jobs
By Insight Global At New York, NY, United States
-Exceptional communication, analytical, presentation and time management skills
-Excellent working knowledge of regulatory compliance requirements and procedures
-Ability to demonstrate impact on project goals through proactive solutions and keeps management aware of project schedules/timelines.
-Knowledge of MS Office suites, database, spreadsheets, graphic and communications applications
-Extensive knowledge of oncology clinical trials and oncology terminology required.
Clinical Research Coordinator Jobs
By Nemours At , Orlando, 32827, Fl
Previous research experience, including qualitative interviewing strongly preferred
Minimum of a bachelor's degree in psychology, pre-med, public health, or related.
Must be able to effectively use Microsoft computer software, SPSS, and REDCap.
Must be able to coordinate and establish priorities among diverse tasks.
Clinical Research Coordinator 2 Jobs
By University of Miami At Miami, FL, United States
Any appropriate combination of relevant education, experience and/or certifications may be considered.
Maintains requisite skills and mandatory training in safety, equality, responsible conduct of research, continuing education, and research competencies.
Assist principal investigators, project managers in coordinating Federal and/or industry-sponsored research studies.
Maintains study binders and filings according to protocol requirements, UM and department policy.
Follows the appropriate fundamental requirements of all international, national, and local regulatory bodies.
Minimum 2 years of relevant experience.
Clinical Research Regulatory Manager
By MBO Partners At Charlotte, NC, United States
5-10 years of clinical trial regulatory management experience.
Quality Management System/Regulatory Compliance Program
5 Years minimum regulatory experience in clinical trials
Regulatory certification from AAAHRP, SOCRA, PRIM&R or similar organizations
Experience gained from multiple perspectives: industry sponsor, CRO, academic, government or site level
Has GCP training and follows GCP guidelines and other guidelines related to the conduct of human subject’s research
Ssu Regulatory Coordinator Jobs
By Syneos Health At United States
Assists SSU staff with the active project management of ongoing contract issues; performs follow-up on all outstanding contract issues.
Associate’s Degree or equivalent combination of education and training preferred.
Good organizational skills and good attention to detail, with proven ability to handle multiple tasks effectively.
Quality-driven in all managed activities.
Strong computer skills, including Word, Excel, PowerPoint, Publisher.
Assists with quality control processes and translation processes related to submissions, contracts and essential documents.
Manager Regulatory Consumer Research
By Philip Morris International At Stamford, CT, United States
Specific Experience Strong statistical and analytical skills as well as in using specialized statistical software (e.g., SPSS, SAS).
Analyze, interpret, present and disseminate post-market study results verbally and in writing, in order to maximize internal knowledge and alignment.
Directly interact with key internal stakeholders including Regulatory Affairs, External Affairs, Scientific Engagement and Consumer Insights.
Technical expertise in design, development, and implementation of pre- and post-market studies in social science, health services, epidemiology, pharmaceutical or tobacco.
Legally authorized to work in the U.S.
We have implemented Smart Work, a hybrid model of working that promotes flexibility in the workplace.
Research & Regulatory Analyst Jobs
By GreenLite Technologies At Texas, United States
Strong organizational skills and extreme attention to detail
Demonstrated ability to manage priorities and projects in a dynamic, fast-paced environment
Working closely with the Head of Research & Regulatory on any ad-hoc, or internal research/regulatory requests or projects.
Ability to read, analyze and translate/summarize government and legal code/statutes - including Building Code, Land Use/Zoning, Development Ordinances, Code Enforcement Policies
Initiative and bias for action, on-time delivery, and operational excellence
Honest and direct without any ego
Clinical Research Associate (Study/Ctms/Regulatory)
By Rangam At United States
What is a nice to have (but not required) regarding skills, requirements, experience, education, or certification?
Required Skill 5: Experience with using clinical trial management systems
What years of experience, education, and/or certification is required?
Required Skill 1: Clinical Research Experience – could be in various roles (study coordinator, regulatory, compliance, safety, etc.)
What are the top 5 skills/requirements this person is required have?
Required Skill 3: Good communication
Research Regulatory Coordinator I
By Intermountain Healthcare At , Murray, 84107, Ut $23.70 - $37.32 an hour
Experience working in a collaboratively in a team environment
Experience using word processing, spreadsheet, database, internet and e-mail and scheduling applications.
The hourly range for this position is listed below. Actual hourly rate dependent upon experience.
Interact with others by effectively communicating, both orally and in writing.
Operate computers and other office equipment requiring the ability to move fingers and hands.
See and read computer monitors and documents.
Clinical Research Regulatory Coordinator
By Medix™ At United States
Experience using standard word processing and data management software programs, including Word and Excel, in order to develop and prepare reports.
Experience creating Informed Consent Documents that comply with HRPP/ IRB policies and procedures, FDA regulations, and sponsor requirements.
Experience with editing, including summarizing information into concise and condense documents.
Knowledge of oncology and hematology.
Experience working with FDA regulations, NCI policies and procedures, and Good Clinical Practice guidelines for the conduct of clinical research.
Working knowledge of Human Research Protections Program (HRPP/IRB) policies and Procedures.
Clinical Research Coordinator (Ft) 8A-5P Research & Academics
By Ballad Health At , Kingsport, Tn

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Clinical Research Coordinator Jobs
By Apsida Life Science At Nebraska, United States
At least 1 year experience as a Clinical Research Coordinator
Demonstrated computer proficiency, specifically with Microsoft Office
I look forward to hearing from you!
Rn - Clinical Research Coordinator (Varied Schedules Open) - Pa
By Navitas Healthcare, LLC At Altoona, PA, United States

The Clinical Research Coordinator Nurse is responsible for coordinating and managing clinical research studies, including patient recruitment, screening, and follow-up. They work closely with ...

Regulatory Coordinator Jobs
By Roper St. Francis Healthcare At Charleston, SC, United States

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Clinical Research Coordinator Jobs
By Medix™ At Las Cruces, NM, United States
May be responsible for regulatory submissions. Need working knowledge of essential documents and IRB requirements
8 month contract, perfect opportunity to gain knowledge with big name trials
Participates in site feasibility determination, site qualification visits, site initiation visits and research related meetings
Part-time, 100% on-site (20 hours/week M-F)
Participates in the identification of potential clinical trial participants, screens them for eligibility, and enrolls participants per protocol
Coordinates the schedule of events for clinical trial participants from screening to follow up according to protocol
Clinical Research Coordinator Jobs
By Northwell Health At , Manhasset, 11030, Ny $58,540 - $92,650 a year
Bachelor's Degree required, or equivalent combination of education and related experience.
Collects labels, logs, processes, and ships biological specimens for analysis according to protocol and training requirements.
1-3 years of relevant experience, required.
Responsible for coordination of a designated study or group of studies.
In research projects, oversees recruitment of subjects, implementation of study procedures, and the collection and processing of data.
Keeps accurate and up-to-date records.
Clinical Research Coordinator Jobs
By Northwestern University At , Chicago, Il
Minimum Competencies: (Skills, knowledge, and abilities.)
Preferred Competencies: (Skills, knowledge, and abilities)
Provides consultation to internal/external project staff on appropriate data management, methodological issues and analysis of data.
Ensures appropriate and timely compliance with associated local, state, & federal regulatory guidelines, requirements, & laws; & research protocols.
Demonstrated knowledge of Alzheimer’s disease and the related dementias
Demonstrated knowledge of federal and state regulations governing the participation of human subjects.
Clinical Research Coordinator Jobs
By The IMA Group At St Louis, MO, United States
Coordinate clinical trials per FDA requirements and GCP guidelines per sponsor protocols.
Acquire detailed knowledge of the protocol and procedures associated with each clinical research study.
Maintain familiarity with each clinical research study’s requirements and apply all applicable regulations accurately.
Additional duties and responsibilities may be assigned as needed.
Strong follow through skills and ability to proactively identify and solve problems, demonstrated initiative is imperative.
Must have strong communication skills, speak, and listen respectfully with the public, physicians, and co-workers.
Assistant Clinical Research Coordinator
By UC San Diego Health At , San Diego, 92093, Ca $29.99 - $48.25 an hour
Experience in medical assessment and patient interviewing to determine toxicities related to protocol management.
Experience using statistical software applications. Knowledge of database, word processing and spreadsheet applications such as Velos, Access, Excel and MS Word.
Experience performing clinical research duties in a clinical research environment.
Experience with laboratory procedures and values and experience in interpreting them to determine patient eligibility and potential toxicities.
Experience working with FDA policies regulating clinical trials.
Experience interpreting medical charts, experience in abstracting data from medical records.