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Clinical associate • hartford ct
- Promoted
Clinical Trials-Hem / Onc-Clinical Research Associate 1- 40hr
Connecticut Children'sHartford, CT, US- Promoted
Clinical Policy Coordinator
Middlesex HealthNew Britain, CT, USClinical Research RN
Hartford HealthCare Corp.Simsbury, CT, United States- Promoted
Associate
The TJX Companies, Inc.Hartford, CT, United StatesClinical Associate Consultant
ITL USAHartford, CT, US- Promoted
Nursing Clinical Coordinator
healthecareersManchester, CT, USCRNA Clinical Coordinator
Yale New Haven HealthHartford, CT, United States- Promoted
Clinical Physical Therapist
MedAdventuresWethersfield, CT, United StatesNursing Clinical Coordinator
Eastern Connecticut Health NetworkManchester, CT, United States- Promoted
Associate
TJXHartford, CT, United States- Promoted
Nursing Clinical Coordinator
ECHNManchester, CT, USClinical Territory Associate - Future Opportunity
Intuitive SurgicalHartford, Connecticut, US- Promoted
Clinical Sales Representative
Cranial TechnologiesHartford, CT, USNursing Clinical Coordinator
GenZJobsManchester, CT, United StatesClinical Supervisor
Aveanna HealthcareHartford, CT, United States- Promoted
Clinical Research Assistant - Clinical Research Center
Hartford HealthCare at HomeHartford, CT, US- Promoted
Associate
Gerber Ciano Kelly Brady LLPRocky Hill, CT, US- Promoted
DH : Full Time OBGYN in CT
Clinical MagnetNewington, CT, USThe average salary range is between $ 42,900 and $ 123,100 year , with the average salary hovering around $ 94,847 year .
- psychiatrist (from $ 200,000 to $ 300,000 year)
- chief medical officer (from $ 237,500 to $ 250,000 year)
- independent contractor (from $ 75,563 to $ 225,000 year)
- principal software engineer (from $ 150,600 to $ 219,381 year)
- software architect (from $ 129,188 to $ 216,300 year)
- federal (from $ 78,804 to $ 212,575 year)
- technical program manager (from $ 158,800 to $ 211,400 year)
- machine learning (from $ 127,850 to $ 211,350 year)
- machine learning engineer (from $ 128,250 to $ 211,350 year)
- software engineering manager (from $ 153,100 to $ 211,350 year)
- Newark, NJ (from $ 71,725 to $ 216,025 year)
- Louisville, KY (from $ 56,096 to $ 215,250 year)
- Irving, TX (from $ 43,875 to $ 200,450 year)
- Cleveland, OH (from $ 99,601 to $ 200,000 year)
- Lincoln, NE (from $ 150,750 to $ 187,852 year)
- Overland Park, KS (from $ 49,332 to $ 180,000 year)
- New York, NY (from $ 70,000 to $ 174,939 year)
- Saint Paul, MN (from $ 70,000 to $ 171,148 year)
- Lansing, MI (from $ 84,125 to $ 168,471 year)
- Raleigh, NC (from $ 91,870 to $ 167,700 year)
The average salary range is between $ 56,533 and $ 157,029 year , with the average salary hovering around $ 83,273 year .
Related searches
Clinical Trials-Hem / Onc-Clinical Research Associate 1- 40hr
Connecticut Children'sHartford, CT, US- Full-time
Job Description
Directly reporting to the Lead Clinical Research Associate for a designated area(s) of the Clinical Trials Department, under limited supervision, coordinates and manages clinical trials in accordance with federal, and state regulations, Institutional Review Board approvals and Connecticut Children's policies and procedures. Under limited supervision, performs a full range of complex, clinical research activities for a broad range of assigned research projects. Works collaboratively with investigators, clinical research nurses, various clinical support services, and external parties (e.g. study Sponsors) to successfully execute trial specific protocol requirements.
Responsibilities
STUDY COORDINATION AND MANAGEMENT (performs responsibilities under limited supervision) :
- Provides support for a minimum of three (3) divisions and / or three (3) investigators that includes two (2) complex clinical trials.
- Ensures compliance with clinical trial protocols and clearly and thoroughly documents each clinical trial participant visit.
- Participates in recruitment and selection of clinical trial participants by reviewing medical history as well as protocol specified inclusion and exclusion criteria.
- Participates in the consent / assent process ensuring the clinical trial participant and family understand all aspects of the study protocol including risks and benefits of participating in the clinical trial.
- Provides timely information regarding each clinical trial visit to all ancillary departments as required e.g., Office for Grants and Sponsored Programs, pharmacy, institutional review board, etc.).
- Completes data collection as specified by the clinical trial protocol.
- Provides timely information to study Sponsors including completion of data queries.
- Oversees the procurement, preparation and shipping of research specimens as needed.
- Meets with the Principal Investigator regularly during the trial to review progress, identify challenges and reconcile issues as necessary; documents meetings with investigators.
- May transport study medication as needed from Connecticut Children's research pharmacy to a Connecticut Children's outpatient clinic in accordance with Connecticut Children's Medication Transportation Policy.
STUDY START-UP / CLINICAL TRIAL INITIATION (performs responsibilities under limited supervision) :
RESEARCH COMPLIANCE (performs responsibilities under limited supervision) :
TRAINING AND EDUCATION :
MENTORING & EDUCATIONAL RESPONSIBILITIES :
Qualifications
Minimum education (degree / type of degree).
Minimum experience (minimum years & type of experience)
Preferred education & experience
License and / or Certification
Required : SOCRA, ACRP or other research professional certification within one (1) year of eligibility; successful completion of the Collaborative Institutional Training Initiative (CITI) Course in the Protection of Human Research Subjects within 3 months of employment.
Preferred : N / A
Knowledge, Skills and Abilities
Knowledge of :
Demonstrates a fundamental knowledge of research protocols including each element of the protocol, investigational product development, clinical research participant safety and related documentation and reporting practices, research regulations, human research protection principals and Good Clinical Practice (GCP) guidelines.
Skilled at :
Ability to :
Work Environment :
Both clinical and non-clinical work environment
About Us
Connecticut Children's is the only health system in Connecticut that is 100% dedicated to children. Established on a legacy that spans more than 100 years, Connecticut Children's offers personalized medical care in more than 30 pediatric specialties across Connecticut and in two other states. Our transformational growth establishes us as a destination for specialized medicine and enables us to reach more children in locations that are closer to home. Our breakthrough research, superior education and training, innovative community partnerships, and commitment to diversity, equity and inclusion provide a welcoming and inspiring environment for our patients, families and team members.
At Connecticut Children's, treating children isn't just our job - it's our passion. As a leading children's health system experiencing steady growth, we're excited to expand our team with exceptional team members who share our vision of transforming children's health and well-being as one team.