We are currently seeking a Clinical Trial Recruitment Associate for a prominent Pharmaceutical client of ours.This position is in New Haven, CT (Hybrid Role).
Details for the position are as follows...serp_jobs.internal_linking.show_moreserp_jobs.last_updated.last_updated_30
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Affinity Hospice Management LLCNew Haven, CT
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Full-Time Clinical Faculty & Clinical Coordinator : Pathologists' Assistant Program
InsideHigherEdHamden, Connecticut, United States
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Constellation Health ServicesOrange, CT, United States
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Abbott Laboratories companyNew Haven, CT, United States
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Solomon PageNew Haven, CT
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We are seeking a Clinical Trial Manager to oversee clinical trial operations, ensuring projects meet quality standards, regulatory compliance, and timeline requirements.
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Quinnipiac UniversityNorth Haven, CT, US
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Yale New Haven HealthNew Haven, CT, United States
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Join a well-established and collaborative Clinical Operations team in a Senior Clinical Trial Manager role with opportunity for career enrichment.
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HIRING ASAP Spanish Speaking Part-Time Clinical Medical Assistant
American Family CareWest Haven, CT, US
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Community Resources for JusticeNew Haven, CT, United States
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The Program Director is responsible for overall operations of managing Dana's House, a Behavioral Health Residential Program.
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We are currently seeking a Clinical Trial Recruitment Associate for a prominent Pharmaceutical client of ours. This position is in New Haven, CT (Hybrid Role). Details for the position are as follows :
Job Description :
Pay : 25.00-32.00 / hr.
Length of Assignment : 17 months with potential for extension or conversion.
Training 4-6 wks onsite. Position will then be mostly remote unless there is a mandatory meeting or additional training.
Responsible for registering new and current clinical research participants and conducting a series of pre-screening procedures to determine eligibility and enroll them for clinical studies.
Maintains first contact with potential participants and informs them about clinical research and available study opportunities
Assesses participants qualifications for participation in a study based on information gathered during the intake in accordance with study protocol inclusion / exclusion criteria and medical guidance
Communicates with participants via text messaging, emailing, and other methods in compliance with regulatory requirements for study related recruitment, follow up, soliciting updated information and regular database clean up
Schedules study screenings and cohorts / groups for dosing according to established timelines and manages appointments
Day-to-Day : clinical trial study pre-screening, participants review of ongoing studies, intake of participant background, and decipher if candidate is a good fit for a study.
Must be available and flexible to work all of the following shifts : Mon-Thu : 7 : 30am-4 : 00pm; 9 : 00am-5 : 30pm; 10 : 00am-6 : 30pm and Fri : 7 : 30am-4 : 00pm; 8 : 00am-4 : 30pm; 9 : 00am-5 : 30pm. Saturday : As needed per level of recruitment activity. Would be given advance notice if Saturday work is needed.