Clinical Research Coordinator Jobs
By RAOOF MD Dermatology At , Encino, 91436, Ca

Facilitate and coordinate the daily clinical trial activities. Responsible for recruitment, patient screening, and enrollment for clinical studies. Schedule and attend study participant ...

Clinical Research Coordinator Jobs
By Piedmont Healthcare At , Atlanta, Ga

Forbes named Piedmont one of Georgia’s 10 best employers and the highest-ranked healthcare provider.

Clinical Research Coordinator Jobs
By Vitalief Inc. At Bryan, TX, United States
Any exposure to EPIC (Electronic Health Records system) and/or OnCore (Clinical Trials Management System) is a plus.
Manage eligibility check lists, perform patient screening/consenting (informed consent), patient activation and managing patient care (patient retention).
Any experience in Oncology and/or working on complex clinical trials is a plus.
Must possess excellent interpersonal skills to interact with patients in a clear and confident manner.
Experience in preparation of documents for submission to the Institutional Review Board (IRB), continuing reviews, and submission of amendments and modifications.
Must have strong Microsoft Office skills.
Clinical Research Coordinator - Houston
By Healthwaze At Bellaire, TX, United States
Manages the inventory of equipment and supplies related to the study.
Responsible for ensuring study compliance with local and federal laws and regulations.
Facilitate regulatory start up-documentation and filings, including central IRB submissions.
Recruits and prescreens potential study participants and may perform intake assessments.
Schedule and coordinate protocol-specified study visits.
Creates and/or maintains all documents and records related to the study.
Clinical Research Coordinator I
By Emory University At , Atlanta, 30303, Ga
Maintains data pertaining to research projects, completes source documents/case report forms, and performs data entry.
Performs related approved responsibilities as required.
(1.) High School Diploma or GED and three years of administrative support experience OR
(3.) Licensed as a practical nurse (LPN) and one year admin support or one year of licensed practical nursing experience OR
Handles or assists with administrative activities generally associated with the conduct of clinical trials.
Orders and maintains equipment and supplies.
Clinical Research Coordinator Jobs
By Massachusetts General Hospital(MGH) At , Boston, 02114, Ma
Strong organizational and time management skills required
Working knowledge of statistics, SPSS, and data management programs desired
Perform clerical/organizational work, quality control, and budget management, if needed
Manage and prioritize multiple projects simultaneously
Data entry and quality control procedures
Adhere strictly to all Institutional Review Board (IRB) guidelines and confidentiality requirements
Clinical Research Coordinator Jobs
By SQRL At Denver Metropolitan Area, United States
Gain experience and build a network in an expanding area of clinical research, including cutting-edge vaccine trials!
Patient Recruitment Experience is preferred
Looking for experienced Clinical Research Coordinators in the Denver Metro area!
1-6 years of experience in clinical research or equivalent medical setting experience
At Least 1 year Phlebotomy, EKG, and/or bladder scan experience
Compensation based on experience: $55-75k

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