3 jobs found in Manchester, CT

Middlesex Health is seeking a Genetics Counselor to provide expert genetic risk assessment, counseling, and testing coordination for patients and families. In this role, you will obtain detailed personal and family histories, interpret complex genetic data, explain test options and results, and support informed decision-making. You will collaborate closely with physicians, oncology, maternal-fetal medicine, and primary care teams to integrate genetics into patient care. The position offers access to multidisciplinary resources, opportunities for professional development, and a patient-centered, community-focused culture in a modern healthcare system. Responsibilities Provide genetic counseling to patients and families across oncology, prenatal, and other specialties Collect and analyze detailed personal and family medical histories Recommend, coordinate, and facilitate appropriate genetic and genomic testing Interpret genetic test results and communicate findings in an...

Responsibilities: SUMMARY The Clinical Research Coordinator (CRC) is responsible for the coordination of daily clinical trial activities. USRC has a research Partnership with the principal investigator (PI) and their physician practice. The local oversight and direction for activities related to the conduct of the clinical research is directed by the PI. The CRC will work collaboratively with the principal investigator (PI), the Sr. Clinical Research Coordinator (SCRC), the clinical site, sponsor(s), clinical research organization(s) (CROs), institutional review boards (IRBs), and study participants to ensure Execution of the clinical trial in accordance with the Study Protocol, the Food and Drug Administration (FDA), International Council for Harmonization of Technical Requirements for Pharmaceuticals for Human Use (ICH) and applicable state and local regulations. The CRC will assist the PI in protecting the rights, safety and welfare of all study participants....

The Senior Clinical Research Coordinator (CRC) will work within the Dana-Farber Milford Satellite location and support the clinical research program and research team in the overall conduct of clinical trials using Good Clinical Practice under the auspices of the Principal Investigator and the Clinical Research Manager. The Senior CRC will be responsible for the primary data collection and management of patient clinical information as it pertains to participation in clinical trials. Ensures timely facilitation of trial assessments per protocol and collection of protocol related samples including shipment to outside entities as required. Will support and maintain participant/subject trial binders and may maintain regulatory binders, to ensure study compliance with all state, federal, and IRB requirements. May be responsible for pertinent IRB protocol submissions. This individual may also screen patients for protocol eligibility, obtain informed consent for non-treatment trials, and...