- Regular communication of study requirements and changes to relevant members of study staff Implement recruitment strategies in order to prescreen, screen, and enroll subjects in active trials Screen subjects for eligibility using protocol specific inclusion and exclusion criteria, documenting each potential participants eligibility or exclusion.
- Acts as a point of reference for study participants by answering questions and keeping them informed of study progress
- Ensure relevant study and subject specific information is entered into the CTMS system on a regular basis. Maintains adequate inventory of study equipment and supplies onsite at all times. .
- Conducts patient visits as outlined within each study protocol.
- Complete study documentation and maintenance of study files including, but not limited to, consent forms, source documentation, progress notes if applicable, case report forms, and investigational accountability forms.
- Maintains ongoing communication with the CRO, sponsor, research participants, Site Manager and PI throughout course of the study.
- Manage the day to day activities of the study including problem solving, communication and protocol management.
- Ensure all safety data is reviewed by the PI in a timely manner.
- Protects the rights and welfare of all human research participants involved in research
- Other duties as assigned.
- Knowledge of grammar, spelling, and punctuation.
- Knowledge of purchasing, budgeting, and inventory control.
- Skill in taking and transcribing dictation and operating office equipment.
- Skill in answering the phone and responding to questions.
- Skill in time management, prioritization, and multitasking.
- Skill in writing and communicating effectively.
- Ability to work under pressure, communicate and present information.
- Ability to read, interpret, and apply clinic policies and procedures.
- Ability to identify problems, recommend solutions, organize and analyze information.
- Ability to multi-task, establish priorities, and coordinate work activities.
- Ability to competently use Microsoft Office, including Word, PowerPoint, Excel, and appropriate practice management software.
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clinical research coordinator
1 week ago
Icon Plc Bristol, CT, United StatesAt ICON, it's our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients' lives. · Our 'Own It' culture is driven by four key values that bring us together as individuals ...
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Clinical Research Coordinator
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DaVita Middlebury, United States850 STRAITS TURNPIKESuite 103, Middlebury, Connecticut, , United States of America · At DaVita Clinical Research, we find that our best leaders are those who create an inspiring vision, have a desire to shape the future of medicine, and empower their team to achieve success. The ...
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Clinical Research Coordinator
1 week ago
Yale University New Haven, United StatesWithin the Department of Neurologys Clinical Research Office and reporting to the Research manager with a focus on movement disorders trials, the Clinical Research Coordinator (CRC) will lead efforts in the execution of research studies within the s Clinical Research, Research Co ...
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Clinical Research Coordinator
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Yale University New Haven, United StatesEssential Duties · 1. Serves as the primary oversight specialist on clinical and operational processes for low to moderately complex studies and non-therapeutic trials. Serves as a supporting clinical research coordinator to CRC/CRN II and Sr. CRC/CRN for highly complex protocols ...
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Clinical Research Coordinator
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Queen Consulting Group, Inc. Roxbury, United StatesMaster's Degree is required (A Bachelor's degree may be considered for candidates with at least 5 years of research experience). Minimum 3 years of clinical research, public health research experience or research working with high-risk patient popula Research Coordinator, Clinica ...
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Clinical Research Coordinator
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Yale University New Haven, United StatesThe Cardiovascular Data Science (Car. DS) Lab at Yale University is currently seeking a Clinical Research Coordinator to join our team. This role offers an opportunity to engage in a range of exciting projects aimed at enhancing patient care through Clinical Research, Research Co ...
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Clinical Research Coordinator
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Yale University New Haven, United StatesEssential Duties · 1. Compares protocols and sponsored projects to confirm consistency between funding proposals/awards and approved protocols. 2. Documents established congruency between funding proposals and approved protocols. 3. Facilitates and/or assists with resolution of a ...
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Clinical Research Coordinator
1 week ago
Yale University New Haven, United StatesEssential Duties · 1. Serves as the primary oversight specialist on clinical and operational processes for low to moderately complex studies and non-therapeutic trials. Serves as a supporting clinical research coordinator to CRC/CRN II and Sr. CRC/CRN for highly complex protocols ...
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Marketing Research Coordinator
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Now IT Works East Hampton, United StatesMarketing Research Coordinator - Connecticut Position · Now IT Works · 10/17/2023 · Job Description · Dear Applicants, · I'm looking for a Connecticut based marketing researchcoordinator who has superior organizational skills, an Internet sleuth and isn'tafraid to pick up the ...
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Research Coordinator- Part time
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Moses/Weitzman Health System Meriden, United States Part time**Job Description Summary:** · **Job Description:** · The Research Coordinator I - Outreach Specialist will be a part of the Patient Engagement Team to conduct engagement, enrollment and retention activities for the _All of Us_ research program. This position will specifically be ...
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Clinical Research Coordinator 2
6 days ago
Yale University New Haven, United StatesThe Clinical Research Coordinator II (CRC II) is responsible for providing research services to patients participating in clinical trials within Yale Cancer Center Clinical Trials Office (CTO). Key responsibilities include overseeing, planning, track Clinical Research, Research C ...
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Clinical Research Coordinator 2
1 week ago
Yale University New Haven, United StatesThe Clinical Research Coordinator II (CRC II) is responsible for providing research services to patients participating in clinical trials supported by the Yale Cancer Center Clinical Trials Office (CTO). Key responsibilities include overseeing, plann Clinical Research, Research C ...
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Clinical Research Coordinator 2
1 week ago
Yale University New Haven, United StatesEssential Duties · 1. Serves as the primary oversight specialist on clinical and operational processes for moderately to highly complex protocols. 2. Manages, implements, and evaluates all aspects of clinical trial conduct including study initiation, execution/maintenance, comple ...
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Clinical Research Coordinator 2
1 week ago
Yale University New Haven, United StatesEssential Duties · 1. Serves as the primary oversight specialist on clinical and operational processes for moderately to highly complex protocols. 2. Manages, implements, and evaluates all aspects of clinical trial conduct including study initiation, execution/maintenance, comple ...
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Clinical Research Coordinator 2
1 week ago
Yale University New Haven, United StatesEssential Duties · 1. Serves as the primary oversight specialist on clinical and operational processes for moderately to highly complex protocols. 2. Manages, implements, and evaluates all aspects of clinical trial conduct including study initiation, execution/maintenance, comple ...
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Clinical Research Coordinator 2
1 week ago
Yale University New Haven, United StatesEssential Duties · 1. Serves as the primary oversight specialist on clinical and operational processes for moderately to highly complex protocols. 2. Manages, implements, and evaluates all aspects of clinical trial conduct including study initiation, execution/maintenance, comple ...
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Clinical Research Coordinator 2
1 week ago
Yale University New Haven, United StatesEssential Duties · 1. Serves as the primary oversight specialist on clinical and operational processes for moderately to highly complex protocols. 2. Manages, implements, and evaluates all aspects of clinical trial conduct including study initiation, execution/maintenance, comple ...
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Clinical Research Coordinator II
2 weeks ago
William W. Backus Hospital Windsor Locks, United StatesWork where every moment matters. Every day, over 30,000 Hartford HealthCare colleagues come to work with one thing in common: Pride in what we do, knowing every moment matters here. We invite you to become part of Connecticut's most comprehensive hea Clinical Research, Research C ...
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Clinical Research Coordinator 2
1 week ago
Yale University New Haven, United States1.Serves as the primary oversight specialist on clinical and operational processes for moderately to highly complex protocols. 2. Manages, implements, and evaluates all aspects of clinical trial conduct including study initiation, execution/maintenance, completion, and administra ...
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Clinical Research Coordinator 2: Float
1 week ago
Yale University New Haven, United StatesThe Clinical Research Coordinator II (CRC II) is responsible for providing research services to patients participating in clinical trials within Yale Cancer Center Clinical Trials Office (CTO). Key responsibilities include overseeing, planning, track Clinical Research, Research C ...
Clinical Research Coordinator - Bristol, United States - GI Associates & Endoscopy Center
Description
GI Alliance is seeking an experienced Clinical Research Coordinator.Duties of this position include, but are not limited to, the following:
Position purpose
The Clinical Research Coordinator (CRC) is a specialized research professional working with and under the direction of the Site Manager and Principal Investigator (PI).
The CRC supports, facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study.
Responsibilities/Duties/Functions/Tasks:
Qualifications
Education:
PhD degree in any subject preferred
Experience:
Minimum 3-5 years of clinical research experience. Experience in phlebotomy preferred
Other Requirements:
None
Performance Requirements:
Please Note:
All job offers are contingent on the successful completion of pre-employment criminal history check.
NOTE:
ALL APPLICATIONS MUST BE COMPLETED IN FULL FOR CONSIDERATION.
No phone calls or agencies, please.
EEO/AA-M/F/disabled/protected veteran