Clinical Research Coordinator - Endocrinology jobs in United States
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MelroseWakefield Hospital · 1 month ago

Clinical Research Coordinator - Endocrinology

MelroseWakefield Hospital is seeking a Clinical Research Coordinator in the Division of Endocrinology. This role involves assisting the Principal Investigator in planning and implementing clinical research studies focused on improving care for people with diabetes and other endocrine conditions.

Health CareHome Health CareMedical Device

Responsibilities

Assists in the recruitment of study participants
Completes follow up with study participants in prescribed settings as required
Completes record abstraction of source documents, conducting required study measurements and completing study Case Report Forms in accordance with best practice methods
Complies with all institutional policies and government regulations pertaining to human subjects protections. Maintains regulatory binders, case report forms, source documents, and other study documents. Monitors the occurrence of clinical adverse events, reporting any to the (PI), the study sponsor and Institutional Review Board
Assists with Institutional Review Board (IRB) requirements for each study including meeting institutional educational requirements, submitting documents for review such as amendments, adverse event reporting and annual reviews
Performs basic laboratory activities as needed
Maintains patient confidentiality per HIPAA regulations and keeps study information in a safe and secure location. Adheres to FDA Good Clinical Practice Guidelines
Identifies and resolves problems with protocol compliance by notifying investigator and as necessary with the protocol sponsor
Arranges necessary tests and procedures in accordance with protocol requirements and reports results to the investigator
Participates in site visits with the study sponsor to review completeness and accuracy of study documentation
Maintains inventory of all study supplies
Assesses potential patients and eligibility for inclusion in a particular protocol based on protocol requirements
Reviews all eligibility and ineligibility criteria in the patient’s record
Verifies information with the physician
Interviews patients to obtain information for eligibility assessment, explain the study, and obtains signature for the informed consent form
Conducts a QC check of completed CRFs prior to submission for data entry
Coordinates resolution of all data queries
Completes data entry as warranted
Performs necessary tests as needed and as appropriate to level of training such as EKGs, Walk tests, etc

Qualification

Clinical research experienceBLS certificationIATA certificationCITI certificationData collection skillsAttention to detailCommunication skillsOrganizational skills

Required

Bachelor's degree OR High School Diploma or equivalent AND Four (4) years of related experience
Basic Life Support (BLS) certification may be required based on specific role requirements
High degree of organizational talents, data collection, and analysis skills
Requires meticulous attention to detail
Excellent computer skills including word processing
Ability to prioritize quickly and appropriately
Excellent communication and interpersonal skills
Systematic record-keeping

Preferred

Two (2) years in research related activities
IATA Hazardous Good Shipping certification
CITI Human Research Protection certification

Benefits

Comprehensive Total Rewards package that supports your health, financial security, and career growth

Company

MelroseWakefield Hospital

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MelroseWakefield Hospital and Lawrence Memorial Hospital provide high-quality, community-based care.

Funding

Current Stage
Late Stage
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