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Clinical Research Trials Coordinator Jobs in 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 Trials Research Assistant - Pediatric Neonatology
By University of Iowa At Iowa City, IA, United States
Bachelor’s degree in a related field or an equivalent combination of education and/or related experience.
Communicates with Research Manager and PIs about the status of the research projects.
Communicates with Research Manager and PI about the status of the research projects.
Excellent written and verbal and interpersonal communication skills.
Ability to manage complex information with attention to detail and a high level of accuracy.
Six months to one year of experience in clinical research
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 Trials Research Assistant - Radiation Oncology
By University of Iowa At Iowa City, IA, United States
Basic experience and participation with clinical trials, following specific protocol techniques and management.
Protocol Development/ Management and Study Responsibilities:
A Bachelor of Science degree of an equivalent combination of education and experience.
Clinical Trials & Data Management Research Assistant
Manages and organizes regulatory documentation from sites and regulatory authorities.
Excellent written, verbal and interpersonal communication 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
Clinical Trials Research Associate - Cancer Center
By University of Iowa At Iowa City, IA, United States
Minimum 1 year of clinical research experience or medical research data management experience.
Bachelor’s degree or an equivalent combination of education and experience.
Assists in the design, development, execution and administration of data entry for protocols and clinical studies.
Follows study participants; manages collection of data including maintaining records of patient visits/interviews.
Excellent verbal, written and interpersonal communication skills.
Ability to manage complex information with attention to detail and a high level of accuracy
Clinical Trials Research Assistant - Cancer Center
By University of Iowa At Iowa City, IA, United States
Bachelor’s degree or an equivalent combination of education and experience
6 to 12 months experience in a research or health care setting
Excellent verbal, written and interpersonal communication skills
Ability to manage complex information with attention to detail and a high level of accuracy
Relevant experience in the conduct of clinical or laboratory research studies
Knowledge of regulatory guidelines and procedures
Clinical Trials Research Associate - Gastroenterology/Hepatology
By The University of Iowa At , Iowa City, Ia
Protocol Development/ Management and Study Responsibilities:
Excellent time management skills and the ability to perform detail oriented work independently is required
Experience with following specific protocol techniques and management is desirable.
Manage and organize regulatory documentation from sites and regulatory authorities.
Manage and organize regulatory documents from sponsors and CROs.
Excellent written and verbal communication skills are required.
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.
Project Leadership - Clinical Trials -
By Parexel At , Remote

The Project Leadership function at Parexel is a critical part of driving success for our clients and advancing clinical research projects. As a part of the Global Project Leadership organization, ...

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 I
By Regions Hospital At , Saint Paul, 55101, Mn
Minimum of two years of experience working in a health care setting
Clinical research experience in a clinical, academic, or industry setting.
Bachelor’s degree in a healthcare, medical or science related 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 Trials Research Assistant - Cancer Center - Flexible
By University of Iowa At Iowa City, IA, United States
Bachelor’s degree or an equivalent combination of education and experience
6 to 12 months experience in a research or health care setting
Excellent verbal, written and interpersonal communication skills
Ability to manage complex information with attention to detail and a high level of accuracy
Relevant experience in the conduct of clinical or laboratory research studies
Knowledge of regulatory guidelines and procedures

Are you looking for an exciting opportunity to join a dynamic team of clinical research professionals? We are looking for a Clinical Research Trials Coordinator to join our team and help us develop and execute clinical trials for our cutting-edge medical products. As a Clinical Research Trials Coordinator, you will be responsible for coordinating all aspects of clinical trials, from protocol development to data collection and analysis. You will also be responsible for ensuring compliance with all applicable regulations and guidelines. If you are a detail-oriented professional with a passion for clinical research, this is the perfect job for you!

Overview:

A Clinical Research Trials Coordinator is responsible for coordinating and managing clinical research trials. This includes recruiting and enrolling participants, collecting and managing data, and ensuring compliance with all applicable regulations.

Detailed Job Description:

Clinical Research Trials Coordinators are responsible for the planning, implementation, and management of clinical research trials. This includes recruiting and enrolling participants, collecting and managing data, and ensuring compliance with all applicable regulations. They must also coordinate with other members of the research team, such as physicians, nurses, and other healthcare professionals. Clinical Research Trials Coordinators must be able to effectively communicate with participants and other members of the research team. They must also be able to interpret and analyze data, and provide feedback to the research team.

What is Clinical Research Trials Coordinator Job Skills Required?

• Excellent communication and interpersonal skills
• Strong organizational and time management skills
• Ability to interpret and analyze data
• Knowledge of applicable regulations and guidelines
• Ability to work independently and as part of a team
• Proficiency in Microsoft Office Suite

What is Clinical Research Trials Coordinator Job Qualifications?

• Bachelor’s degree in a related field
• At least two years of experience in clinical research
• Certification in clinical research (optional)

What is Clinical Research Trials Coordinator Job Knowledge?

• Knowledge of clinical research protocols and procedures
• Knowledge of applicable regulations and guidelines
• Knowledge of data collection and analysis
• Knowledge of medical terminology

What is Clinical Research Trials Coordinator Job Experience?

• Experience in clinical research
• Experience in data collection and analysis
• Experience in recruiting and enrolling participants

What is Clinical Research Trials Coordinator Job Responsibilities?

• Recruit and enroll participants for clinical research trials
• Collect and manage data for clinical research trials
• Ensure compliance with all applicable regulations and guidelines
• Coordinate with other members of the research team
• Interpret and analyze data
• Provide feedback to the research team