Clinical Research Coordinator

Cardio Metabolic Institute is a multi-specialty group with a small research division. We are seeking an experienced clinical research coordinator to help with existing and new clinical trials. > 1 year of experience as a clinical research coordinator a must Job Requirements Notify subjects regarding all study aspects relevant to them. Enter study data into the applicable database. Keep track of study activities to make sure compliance with protocols and with all related local, state, and national regulatory and institutional polices. Manage necessary records of study related activity which includes case report forms, drug dispensation records etc. Communicate with laboratories or researchers about laboratory findings. Direct the request, collection, labelling, storage, or shipment of samples. Enroll subjects in the study as per the study protocol. Prepare or get involved in quality assurance audits performed by study sponsors, regulatory authorities, or exclusively designated review groups. Prepare advertising and other educational materials and conduct campaigns to enroll subjects. Arrange space for study equipment and other trial related material. Monitor enrolment status of participants and record dropout details such as dropout causes and subject contact efforts. Overview proposed study protocols to assess factors such as sample collection procedures, data management issues, and possible subject threats. Record adverse event and side effect information and consult with investigators concerning the reporting of events to regulatory agencies. Prepare trial-related paperwork such as protocol worksheets, adverse event reports, IRB documents, procedural manuals and progress reports. Manage subject registration to make sure that informed consent is effectively obtained and recorded. Keep in touch with sponsors to schedule and coordinate site visits or to answer queries. Dispense study medical devices or drugs to subjects, determine dosages and deliver instructions as necessary. Full time. Typical schedule will be from 8 to 430. Flexibility for an earlier or later start to the day and some availability on an some Saturdays for a meeting a must. Need to be personable and a team player. Eligibility for benefits below is after 90 days after start date.

Job Type:

Full-time Pay:

$23.00

• $28.

00 per hour

Benefits:

401(k) Dental insurance Flexible schedule Health insurance Paid time off Vision insurance

Work Location:

In person Clinical Research Coordinator 51 Veronica Avenue, Somerset, NJ 08873 $23

• $28 an hour
• Full-time $23
• $28 an hour
• Full-time Cardio Metabolic Institute is a multi-specialty group with a small research division.

We are seeking an experienced clinical research coordinator to help with existing and new clinical trials. > 1 year of experience as a clinical research coordinator a must Job Requirements Notify subjects regarding all study aspects relevant to them. Enter study data into the applicable database. Keep track of study activities to make sure compliance with protocols and with all related local, state, and national regulatory and institutional polices. Manage necessary records of study related activity which includes case report forms, drug dispensation records etc. Communicate with laboratories or researchers about laboratory findings. Direct the request, collection, labelling, storage, or shipment of samples. Enroll subjects in the study as per the study protocol. Prepare or get involved in quality assurance audits performed by study sponsors, regulatory authorities, or exclusively designated review groups. Prepare advertising and other educational materials and conduct campaigns to enroll subjects. Arrange space for study equipment and other trial related material. Monitor enrolment status of participants and record dropout details such as dropout causes and subject contact efforts. Overview proposed study protocols to assess factors such as sample collection procedures, data management issues, and possible subject threats. Record adverse event and side effect information and consult with investigators concerning the reporting of events to regulatory agencies. Prepare trial-related paperwork such as protocol worksheets, adverse event reports, IRB documents, procedural manuals and progress reports. Manage subject registration to make sure that informed consent is effectively obtained and recorded. Keep in touch with sponsors to schedule and coordinate site visits or to answer queries. Dispense study medical devices or drugs to subjects, determine dosages and deliver instructions as necessary. Full time. Typical schedule will be from 8 to 430. Flexibility for an earlier or later start to the day and some availability on an some Saturdays for a meeting a must. Need to be personable and a team player. Eligibility for benefits below is after 90 days after start date.

Job Type:

Full-time Pay:

$23.00

• $28.

00 per hour

Benefits:

401(k) Dental insurance Flexible schedule Health insurance Paid time off Vision insurance

Work Location:

In person