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Baystate Health · 1 day ago

Clinical Research Coordinator I

Springfield, Massachusetts

Full-time

Onsite

New Grad, Entry Level

$60K/yr - $81K/yr

Baystate Health is a healthcare organization seeking a Clinical Research Coordinator I. The role involves managing research protocols, ensuring subject enrollment goals are met, and collaborating with various stakeholders to facilitate successful study execution.

DeliveryFitnessHealth CareHospitalMedical DeviceStaffing Agency

Responsibilities

Conducts study tasks that are moderately complex in accordance with established protocols or guidelines

Works with patients & families. May conduct screening of patients for inclusion in non-interventional studies based on predetermined criteria

Assists with study procedures and the collection of complex data

Assists in screening of patients for inclusion in interventional studies based on predetermined criteria

Assists with/conducts informed consent process for non-interventional studies with the PI/SubI available for questions

Assists with the informed consent process for interventional studies

Assists with patient education regarding protocol and requirements

Contributes to preparation, submission, and maintenance of regulatory documents

Contributes to and maintains study and patient files in a highly organized manner

May contribute to development of study specific source and site documentation. Secures study and patient files to ensure confidentiality

Performs actual tasks. Records & Organizes Data. Contributes to and maintains source documents and case report forms

Compiles information for interpretation

Works in collaboration with IRB, SPA, and other BMC areas for study success

Responsibilities may include meetings and collaboration with sponsor/CRO for study success

Responsibilities may include travel as needed for Investigator Meetings, etc

May assist in coordinating and supervising assigned study activities

May assist with training of lesser qualified study personnel

Provides feedback on the performance of Research Assistant staff for performance evaluation purposes

Qualification

Medical terminologyStateFederal RegulationsClinical research certificationInterpersonal skillsTime management

Required

High School / GED

Solid knowledge of medical terminology

Solid knowledge of State and Federal Regulations and Guidance's as they relate to research

Highly detail-oriented individual with excellent interpersonal and time management skills

Holds specialty certification in clinical research through an approved accrediting organization or college/graduate program. Must obtain CCRP certification when eligible, it may take up to 2 years to be eligible