Top 13 Clinical research associate Jobs in Farmington Ct

Clinical Research Associate - Clinical Research Center
Hartford Hospital —Hartford, CT
- Full-time
- 5 years
- Mid-level
- Master's degree
Quick Apply
Clinical Trial Research Assistant
Central Connecticut Dermatology —Cromwell, CT
- Full-time
- Microsoft Excel
- Computer literacy
- Outpatient experience
- Health insurance
- Dental insurance
Quick Apply
SP - Staff Nurse
University of Connecticut —Farmington, CT
- $66.96 an hour
- Temporary
- Nursing
- RN License
- Computer literacy
SP - Research Nurse
University of Connecticut —Farmington, CT
- $35.12 an hour
- Temporary
- Nursing
- Patient monitoring
- RN License
SP - Clinical Research Assistant I
University of Connecticut —Farmington, CT
- $20 an hour
- Temporary
- Math
- Bachelor's degree
- Psychology
2d
Research Associate 1
Connecticut Children's Medical Center —Hartford, CT
- Microsoft Word
- Windows
- Master's degree
Per Diem Clinical Research Nurse - Home Visits
Science 37 —Hartford, CT
- $50 - $55 an hour
- Nights as needed
- Nursing
- RN License
- BLS Certification
Clinical Research Coordinator II - Biospecimen
Hartford HealthCare Corp. —Hartford, CT
- Full-time
- Nursing
- Mid-level
- Bachelor's degree
Quick Apply
7d
Research Associate 2
University of Connecticut —Farmington, CT
- Weekends as needed
- Maintenance
- Mid-level
- 3 years
Bilingual Travel Research Coordinator
Moses / Weitzman Health System —Meriden, CT
- Weekends as needed
- Spanish
- English
- Mid-level

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Clinical Research Associate - Clinical Research Center
Hartford Hospital —Hartford, CT
While the Principal Investigator is primarily responsible for the overall design, conduct, and management of the clinical trial, the CRA leads, facilitates and…
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During these visits, you will review essential documents, assess protocol adherence, oversee data entry and query resolution, and ensure maintenance of both the…
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The study monitor will review and provide feedback on study related documents, such as the study protocol, consent form, case report forms, and the clinical…
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Clinical Research Associate - Clinical Research Center

Hartford Hospital -
Hartford, CT

Quick Apply

Job Details

Full-time

Qualifications

Optimizing workflow processes
Collaborate with healthcare professionals
Clinical staff performance evaluation
Biology
Student supervision
Staff performance monitoring
Staff supervision
Performance improvement leadership
Team member evaluation
Healthcare staff management
Informed consent
Research manuscripts
Research ethical considerations
Conference papers
5 years
Bachelor's degree in psychology
Scientific posters
Mid-level
Bachelor's degree in biology
Master's degree
Clinical audit and monitoring
Research project technical leadership
Clinical staff training
Policy & process development
Professional development support
Clinical training
Health information data integrity
Team training
Clinical program monitoring
Quality improvement

Full Job Description

Location Detail: 80 Seymour Street (10008)

Work where every moment matters.

Every day, more than 40,000 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.

***This is a grant funded position***

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.

As an Equal Opportunity Employer/Affirmative Action employer, the organization will not discriminate in its employment practices due to an applicant’s race, color, religion, sex, sexual orientation, gender identity, national origin, and veteran or disability status.

Quick Apply

Refine Your Search

clinical research associate jobs in farmington ct

Clinical Research Associate - Clinical Research Center

Clinical Trial Research Assistant

SP - Staff Nurse

SP - Research Nurse

SP - Clinical Research Assistant I

Research Associate 1

Per Diem Clinical Research Nurse - Home Visits

Clinical Research Coordinator II - Biospecimen

Research Associate 2

Bilingual Travel Research Coordinator

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