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Clinical Research Coordinator 229228 Jobs in Sac, Iowa

Clinical Research Coordinator Jobs
By Northwell Health At , Lake Success, 11020 $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 Ii
By Sutter Health At , Palo Alto $40.85 - $61.28 an hour
Mentors and fosters a constructive teaching environment that helps students and new teammates build confidence in their skills, knowledge and abilities.
Performs information management functions, including maintaining databases, entering and auditing data, may perform trending.
Ensures compliance with protocol guidelines and requirements of regulatory agencies.
2 years experience conducting clinical research.
2 years experience ensuring compliance with research regulations.
Equivalent experience will be accepted in lieu of the required degree or diploma.
Clinical Research Coordinator 1 Jobs
By Baylor Scott & White Health At , Dallas, 75246
Implements various protocols for assigned research projects with appropriate departments throughout the organization by interacting with PIs, clinical managers and supervisors.
Obtains knowledge of departmental functions through reading literature, attending workshops, seminars and conferences and participating in professional organizations.
Research certification or other certifications per specialty area preferred.
Proven written and oral communication skills.
Exceptional computer skills, including Microsoft Office.
Ability to manage time reactive projects in order to meet deadlines.
Clinical Research Coordinator Jobs
By Banner Health At , Gilbert, 85234
This position will support clinical trials for solid tumor patients
This position is Monday - Friday 8am-5pm, No weekends, no holidays!
Our organization supports a drug-free work environment.
Clinical Research Project Coordinator
By Kelly Science, Engineering, Technology & Telecom At Cincinnati Metropolitan Area, United States
● Works under the direction of experienced project clinical trial managers to assist with day-to day
Hybrid (3 days onsite, 2 days remote)
● Bachelor's Degree in a scientific or healthcare-related field or relevant experience
● Minimum of 3 years applicable experience required.
● Proficiency in Microsoft Office and experience with EDC systems
● Excellent communication, organizational, and interpersonal skills
Clinical Research Coordinator Jobs
By Medix™ At Cincinnati Metropolitan Area, United States
Coordinates patient care in compliance with protocol requirements
Disburses investigational drug and provide patient teaching regarding administration and other patient educational needs
Screens potential patients for protocol eligibility
Presents trial concepts and details to the patients, participates in the informed consent process, and enrolls patients on clinical trials
Responsible for review of consents to ensure proper execution of the informed consent process for study subjects
Oversees the preparation of orders by physicians to assure that protocol compliance is maintained
Senior Clinical Research Coordinator
By SAGE Therapeutics At , Remote $78,750 - $108,281 a year
Experience, Education and Specialized Knowledge and Skills
Experience with eTMF; ability to directly apply essential document knowledge to file documents accordingly based on the DIA reference model.
Coordinate and manage version control of clinical documents.
Assist Study Manager with reference searches in support of protocol development.
Assist Study Manager with data reviews.
Co-monitor with Study Manager or designee.
Clinical Research Coordinator Jobs
By Valley Medical Center At , Renton, Wa $63,857 - $96,426 a year
Must have a working knowledge and be skilled in the use of personal computers, information storage and retrieval systems.
Coordinate with Health Information Management to assure appropriate identification of research protocol participants in the electronic health record.
Management of all miscellaneous tasks involved with coordinating clinical trials
Four year degree preferred, national certification a plus.
Minimum 1 year of experience in a clinical research environment.
Performs other related job duties as required.
Clinical Research Coordinator Ii: Cardiology, Ft
By Prisma Health At , Greenville, 29605, Sc
This is a non-management job that will report to a supervisor, manager, director or executive.
The following requirements will also be considered in lieu of 1 year research experience:
If Allied Health Degree: South Carolina certification/license in field.
In lieu of the Above Minimum Requirements
Associate Degree in Allied Health plus 3 years direct experience in that field
OR Bachelor Degree in a science and 3 years direct experience in that field.
Clinical Research Coordinator Jobs
By University of California, Davis At , Davis, 95616, Ca $30.03 - $48.29 an hour
Project management and organizational skills for coordinating aspects of research studies.
Data management experience. Ability to design and maintain an efficient filing and record keeping system.
Knowledge and experience with industry sponsored research.
CITI Certification for Biomedical Researchers and Good Clinical Practice (GCP) Certification after date of hire
Several years of Clinical Research Coordinator experience, with demonstrated increasing level of responsibility is preferred
Experience working with older adult population with cognitive impairment.
Clinical Research Coordinator Jobs
By SRG At Springfield, Illinois Metropolitan Area, United States

Job Title: Clinical Research CoordinatorLocation: Springfield, IL Worksite: OnsiteJob Type: Permanent Full-Time We are searching for a permanent full-time Clinical Research Coordinator who has ...

Account Coordinator/Manager, Clinical Research
By Clinitiative Health Research At Dallas, TX, United States
Works on client clinical trial pipeline to secure study award
Persists to locate appropriate contacts for trial updates and outreach
Demonstrates basic understanding of clinical research
Acts on behalf of sites to sponsors to ensure consideration for feasibility and award
Communicates study updates to sites and other staff members
Completes multiple competing tasks in expected timelines
Clinical Research Coordinator Ii
By UAMS - University of Arkansas for Medical Sciences At Little Rock, AR, United States
Bachelor’s degree plus 3 years general research experience w/demonstrated proficiency in study planning/development, study coordination/management, and/or data collection, or
Associate’s degree plus 5 years clinical research experience, w/demonstrated proficiency in study planning/development, study coordination/management, and/or data collection, or
High School diploma/GED plus 7 years clinical research experience w/demonstrated proficiency in study planning/development, study coordination/management, and/or data collection
UAMS offers amazing benefits and perks
Education discount for staff and dependents (undergraduate only)
Career Training and Educational Opportunities
Clinical Research Coordinator Jobs
By Medasource At New York, United States
1+ years of Clinical Research Coordination experience
Resilient in recovering from setbacks and skilled at finding detours around obstacles.
Ensure data quality and integrity throughout the life of the study.
Collaborate with members of the research and care teams across MSK regarding data input.
Generate data reports and deliver to all necessary parties on the progress of the research project, database, or protocol.
Ensure all appropriate Institutional, State, and Federal regulations throughout the study are followed.
Clinical Research Coordinator Jobs
By SMCI At San Francisco Bay Area, United States
Education: BS/BA degree in a life science, health science, RN, or related field.
2+ years of professional working experience as a Clinical Research Coordinator.
Working knowledge of GCP and FDA Regulations.
Excellent oral and written communication skills.
Strong attention to detail and organizational skills.
Experience utilizing Electronic Data Capture (EDC) systems for clinical studies.
Clinical Research Coordinator Jobs
By SeattleNTC At Greater Seattle Area, United States
$25-$30 per hour depending on experience
2+ years of Clinical Research experience
Experience administering questionnaires (for example, WASI-II, other IQ assessments, MADRS, CAPS-5)
Experience with clinical research protocols, regulatory compliance, and submission processes
Mental health experience a plus
Seattle and Bellevue clinics (must be able to work at both)
Clinical Research Coordinator Jobs
By CAMRIS At Bethesda, MD, United States
Knowledge of clinical quality management and systems (such as Veeva, Master Control, etc.) is preferred.
Assist in the management of Division contract records. Tasks include the following:
CAMRIS International LLC offers competitive salaries and comprehensive benefits. Please submit your resume online at
Minimum of five (5) years of experience in clinical research or a related field.
Excellent communication, grammar and writing skills required.
Demonstrated superior knowledge of research protocols and clinical, scientific and/or medical terminology.
Clinical Research Coordinator - Manager
By Medix™ At San Antonio, Texas Metropolitan Area, United States
Clearly and concisely document patient assessments, observations, test results and other study related information per federal regulations, protocol requirements and GCPs;
Obtain patient informed consent according to federal regulations, GCPs and IRB requirements;
Schedule and conduct patient visits according to protocol requirements and timelines;
Read, understand and is able to accomplish protocol specified patient visits and procedures;
Maintain accurate and complete written source documentation of patient visits and protocol related activities;
Accurately complete case report forms (CRFs &/or eCRFs) and/or worksheets generated by the sponsor;
Clinical Research Coordinator/Project Manager
By K2 Medical Research At Orlando, FL, United States
Strong time management and organizational skills In depth knowledge of industry regulations
Outstanding verbal and written communication skills
Excellent interpersonal and customer services skills
Prior experience in a clinical environment preferred. Experience in clinical research is ideal.
LPN, RN, or other medical licensure or certification preferred.
Strong working knowledge of GCP and FDA guidelines
Clinical Research Coordinator Jobs
By Yuma Clinical Trials At Yuma, AZ, United States

CRC

Junior Clinical Research Coordinator
By Axiom Resource Management At , Nellis Afb, 89191
Coordinate with study auditors, regulatory agencies, collaborators, and sponsors in management of research studies.
Must have current Basic Life Support (BLS) certification within 15 days of hire.
Superb organization skills with a high level of attention to detail.
Refined interpersonal and communication skills.
Experience working within the Military Healthcare System preferred.
Send resume and salary requirements to:
Clinical Research Coordinator 046705 Jobs
By Wayne State University At , Detroit From $51,373 a year

H06 - School of Medicine

Hospital, outpatient clinic and office environments.

Clinical Research Coordinator Jobs
By Sundance Clinical Research At Greater St. Louis, United States

Experienced Clinical Research Coordinator (CRC)

Clinical Research Coordinator Jobs
By Rady Children's Hospital-San Diego At San Diego County, CA, United States

Job Summary: Initiates & manages multiple cooperative group trials such as Children's Oncology Group (COG) clinical trials related to pediatric cancer to include, but not limited to: execution ...

Clinical Research Coordinator Jobs
By Duke University At , Durham, 27710
May develop resources and tools for management of international studies, and/or coordinate with other entities or offices.
Proactively seeks opportunities to add relevant skills and certifications to own portfolio.
Knowledgeable in regulatory and institutional policies and processes; applies appropriately in study documentation, protocol submissions, and SOPs.
Develops data entry or collection SOPs or tools.
Recognizes and reports security of physical and electronic data vulnerabilities.
Uses required EMR functionalities to manage participants and study visits.
Clinical Research Coordinator Jobs
By Mayo Clinic At , Scottsdale, 85259 $29.39 - $44.09 an hour

Graduate or diploma from a study coordinator training program is preferred. Medical terminology course preferred.

Affirmative Action and Equal Opportunity Employer

Dps Clinical Research Coordinator
By City of Hope At Duarte, CA, United States
Bachelor’s Degree or Certified CRA or Certified Tumor Registrar in lieu of degree. Experience may substitute for minimum education requirements.
Basic education, experience and skills required for consideration:
Preferred education, experience and skills:
Conducts protocol database management for an assigned set of multiple research protocols.
Makes recommendations and participates in Policy and Procedure development regarding particular areas of team assignment and general data management issues.
Identifies and communicates important protocol and data management issues or problem areas to supervisor.
Clinical Research Coordinator (Neurology - Movement Disorders)
By Mayo Clinic At , Scottsdale, 85259 $29.39 - $44.09 an hour

Affirmative Action and Equal Opportunity Employer

Clinical Research Coordinator Jobs
By Phoenix Children's Hospital At , Phoenix
Creates study budgets and works with management to determine financial feasibility and resources necessary to conduct the trial
Reviews all regulatory requirements to ensure implementation of appropriate methods, practices, and procedures for all research activities in designated area
With the principal investigator, explains the study purpose, parameters, and requirements of the studies to the participants
Completes case report forms, data entry, and maintains source documentation for all study participants
Offering the most comprehensive care across ages, communities and specialties
Advancing education and training to shape the next generation of clinical leaders