Clinical Research Coordinator jobs in Connecticut
Clinical Research Coordinator organizes research information for clinical projects. Selects and observes subjects and assists with data analysis and reporting. Being a Clinical Research Coordinator oversees experiment scheduling and collection of data. Requires a high school diploma or equivalent. Additionally, Clinical Research Coordinator typically reports to a supervisor or manager. The Clinical Research Coordinator works under moderate supervision. Gaining or has attained full proficiency in a specific area of discipline. To be a Clinical Research Coordinator typically requires 1-3 years of related experience. (Copyright 2024 Salary.com)
Recently Added Clinical Research Coordinator jobs
- Hartford Hospital
-
Bridgeport, CT
FULL_TIME
-
Description
Job Schedule: Full Time
Standard Hours: 40
Job Shift: Shift 1
Shift Details: Flexibility required with some evenings and weekends possible.
Work where every moment matters.
Every day, almost 30,000 Hartford HealthCare employees 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 healthcare network.
Hartford Hospital is one of the largest and most respected teaching hospitals New England. We are a Level 1 Trauma Center that provides cutting edge treatment to its patients. This is made possible by being home to the largest robotic surgery center in the Northeast and the Center for Education, Simulation and Innovation (CESI), one of the most-advanced medical simulation training centers in the world. When hospitals cannot provide the advanced care, expertise and new treatment options their patients require, they turn to us.
Job Summary:
As a specialized research professional the Clinical Research Associate (CRA) collaborates with the Principal Investigator (PI) in leading all activity associated with research study protocols. This includes but is not limited to; research conduct, budget negotiation & management, initiating collaborations with other investigators and areas pertinent to the performance of the study, monitoring research progress and making necessary changes towards process improvement, leading efforts to initiate new studies, attending IRB meetings to expedite the start-up process. The CRA supervises all study activity and may delegate responsibilities to Research Assistants and/or Research Associates as appropriate. In addition, the CRA supervises HHC approved Research Volunteers. While the Principal Investigator is primarily responsible for the overall design, conduct, and management of the clinical trial, the CRA leads, facilitates and coordinates all clinical trial activities playing a critical role in the supervision and conduct of the study. By performing these duties, the CRA works with the PI, department, sponsor, IRB and institution to support and provide guidance on the administration of the compliance, financial, personnel and all aspects of the clinical study.
Job Responsibilities:
- Compiles and extracts data by performing and reviewing patient information to ensure integrity of patient data for analysis and development of protocols.
- Enrolls patients in studies by screening for eligibility criteria, consulting with physicians and obtaining patient informed consent to ensure patient safety preserved and regulatory standards are met.
- Instructs hospital staff and physicians on current study by familiarizing them with protocol requirements to assure proper execution.
- Works effectively as a team member both within and across clinical settings to promote an integrated delivery of health care services through communication, cooperation and collaboration.
- Train, mentor and supervise lower level research staff, students, interns, and volunteers
- Assign tasks to Clinical Research Assistants and Clinical Research Associates as appropriate in collaboration with the CRC manager
- Support other staff in all aspects of study conduct including, oversight associated with meeting the goals outlined in the protocol and clinical trial agreement
- Motivate others, monitor study performance and lead study meetings
- Manage complex multisite, interventional high risk drug/device research protocols
- Presents at conferences (abstracts, poster presentations) and assists in preparation of manuscripts
- Must have in depth knowledge of at least one clinical area
- Serve as CRC leader internal/external, advising other staff regarding complex protocols and projects in one or more clinical area
- Provide a leadership role in developing, implementing, and evaluating the conduct of clinical research
- Takes a lead role and/or coordinates or presents at internal external clinical research education event/conferences
- Lead activities designed to improve organizational performance metrics
- Reviews and develops a familiarity with the clinical trial agreement and/or award terms and conditions. Works with the PI to assure that the study is in compliance with all terms and conditions, including but not limited to education, IRB (HRPP) approval, conflict of interest disclosure, health and safety protections for participants and staff and any financial terms or conditions
- Coordinates appropriate and timely payments to participants (if applicable) in accordance with policies and procedures
- Contributes directly regarding continued and yearly performance appraisal of Clinical Research Center team members
- Promotes and monitors lower level personnel regarding the ethical conduct of research by assuring that good faith suspicions of misconduct in research as defined within Research Administrations Policy and other misconduct as described in HHC Code of Conduct are reported appropriately.
- Registers (if required) studies on ClinicalTrials.gov and maintains current and accurate information
- Coordinates all aspects of study activity as required of a Clinical Research Associate
Qualifications
- Bachelor degree in an appropriate science discipline such as biology, psychology, etc.
- On a case by case basis, Associate degree may be considered with significant years of research experience. Master's Degree preferred
- Five years of clinical research experience.
- Or, seven years of practical clinical research experience is required with an Associate degree.
We take great care of careers.
With locations around the state, Hartford HealthCare offers exciting opportunities for career development and growth. Here, you are part of an organization on the cutting edge - helping to bring new technologies, breakthrough treatments and community education to countless men, women and children. We know that a thriving organization starts with thriving employees- we provide a competitive benefits program designed to ensure work/life balance. Every moment matters. And this is your moment.
- 29 Days Ago
- Clinical Management Consultants
-
Norwich, CT
FULL_TIME
- Are you ready to take your nursing career to the next level? An exciting opportunity awaits you at one of Coastal Connecticut's premier hospitals – a multiple award-winning institution that sets the s...
- 15 Days Ago
- Clinical Management Consultants
-
Middletown, CT
FULL_TIME
- Expand your nursing career with a new opportunity available as an Infection Prevention Nurse Coordinator at a top performing hospital near the Naugatuck River in Connecticut. With 300 beds, this hospi...
- 18 Days Ago
- Clinical Management Consultants
-
Marlborough, CT
FULL_TIME
- An established acute care hospital located in eastern Connecticut is currently searching for an experienced Operating Room Assistant Nurse Manager to join their award-winning organization. This not-fo...
- 1 Month Ago
- Clinical Management Consultants
-
Stamford, CT
FULL_TIME
- A Magnet designated hospital located in Southern Connecticut is currently searching for an experienced Critical Care Clinical Coordinator to work the night shift at their reputable hospital facility. ...
- 15 Days Ago
- University of Connecticut (Uconn) Health
-
Farmington, CT
OTHER
- Job DetailJob Title:Clinical Research TechnicianDepartment:10400-Ctr for Molecular OncologyLocation:FarmingtonFTE%:1Shift1stSearch #:2024-992Closing Date:04/11/2024Recruiter:Rucker, Pamela S.Additiona...
- 14 Days Ago
Clinical Research Coordinator jobs at Popular Companies
- Medix™
-
Pittsburgh, PA
- Duration: 3 month contract Schedule: 24 hours per week (part time between Monday through Friday, 8AM-5PM EST) Location: ...
- 4/23/2024 12:00:00 AM
- Schwarzman Animal Medical Center
-
New York, NY
- Department: Clinical Services Clinical Research Coordinator Clinical Research Coordinator Summary The Schwarzman Animal ...
- 4/23/2024 12:00:00 AM
- Cook County, IL
-
Chicago, IL
- This position is exempt from Career Service under the CCH Personnel Rules. Job Summary The Clinical Research Coordinator...
- 4/23/2024 12:00:00 AM
- Diabetes Research Center
-
Tustin, CA
- Company Description: The Diabetes Research Center is a highly reputable, private company dedicated to clinical trials in...
- 4/23/2024 12:00:00 AM
- Beth Israel Lahey Health
-
Boston, MA
- When you join the growing BILH team, you're not just taking a job, you're making a difference in people's lives. Job Typ...
- 4/21/2024 12:00:00 AM
- CARLE
-
Peoria, IL
- Promotes good clinical practices in the conduct of clinical investigations by possessing an in-depth knowledge of federa...
- 4/20/2024 12:00:00 AM
- Virginia Commonwealth University
-
Richmond, VA
- Virginia Commonwealth University (VCU) School of Medicine is a premier academic medical center located in the heart of R...
- 4/20/2024 12:00:00 AM
- NYU Langone Health
-
New York, NY
- NYU Grossman School of Medicine is one of the nation's top-ranked medical schools. For 175 years, NYU Grossman School of...
- 4/19/2024 12:00:00 AM