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Remote Clinical Research Coordinator Jobs in Texas

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.

Associate Clinical Administrative Coordinator - National Remote
By UnitedHealth Group At , Dallas, 75202, Tx $16.00 - $27.31 an hour
Manage the intake of members or the admission/discharge information post notification
Work with hospitals, clinics, facilities and the clinical team to manage requests for services from members and/or providers
Manage the referral process, processing incoming and outgoing referrals and prior authorizations, including intake, notification and census roles
1+ years of customer service experience analyzing and solving customer problems
Experience working within the health care Industry and with health care insurance
Experience working with Medicare and/or Medicaid Services
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 a rewarding career in clinical research? We are seeking a Remote Clinical Research Coordinator to join our team and help us advance medical research. You will be responsible for managing clinical trials, ensuring compliance with regulatory standards, and providing support to research teams. If you are passionate about making a difference in the medical field, this is the perfect opportunity for you!

Overview A Remote Clinical Research Coordinator is responsible for coordinating and managing clinical research activities in a remote setting. This includes working with clinical research teams, sponsors, and other stakeholders to ensure that research protocols are followed and that data is collected, analyzed, and reported accurately. Detailed Job Description The Remote Clinical Research Coordinator is responsible for the coordination and management of clinical research activities in a remote setting. This includes working with clinical research teams, sponsors, and other stakeholders to ensure that research protocols are followed and that data is collected, analyzed, and reported accurately. The Remote Clinical Research Coordinator is also responsible for the development and implementation of research protocols, the collection and analysis of data, and the preparation of reports and presentations. The Remote Clinical Research Coordinator must be able to work independently and collaboratively with other team members. Job Skills Required
• Knowledge of clinical research protocols and regulations
• Ability to work independently and collaboratively
• Excellent organizational and communication skills
• Proficiency in data analysis and reporting
• Ability to manage multiple projects simultaneously
• Knowledge of computer systems and software
Job Qualifications
• Bachelor’s degree in a related field
• At least two years of experience in clinical research
• Knowledge of Good Clinical Practice (GCP)
• Ability to work in a remote setting
Job Knowledge
• Knowledge of clinical research protocols and regulations
• Knowledge of Good Clinical Practice (GCP)
• Knowledge of computer systems and software
Job Experience
• At least two years of experience in clinical research
• Experience in data analysis and reporting
• Experience in project management
Job Responsibilities
• Develop and implement research protocols
• Collect and analyze data
• Prepare reports and presentations
• Manage multiple projects simultaneously
• Ensure compliance with clinical research protocols and regulations
• Communicate with clinical research teams, sponsors, and other stakeholders
• Work independently and collaboratively with other team members