Headlands Research
Clinical Research Coordinator
Headlands Research, Pikesville, Maryland, United States, 21208
Overview
At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. We're an exceptional family of next-generation clinical trial sites, integrating cutting edge technology and high-quality support services, and significantly expanding participant engagement Founded in 2018, our company operates 18 clinical trial sites in the US and Canada with rapid plans for expansion.
The Role
Pharmasite, a Headlands Research site, is looking for a Clinical Research Coordinator to manage clinical research protocols. This individual will work directly with the investigators, and other research staff to ensure protocol visits are being conducted according to ICH GCP guidelines.
Responsibilities
Comprehend study design of each protocol that is assignedPerform procedures in compliance with the study protocolRecruit and screen study subjects according to specific protocol requirementsCollect and record study data in source documents via electronic system (CRIO)Manage study related activitiesAdherence to protocol requirementsReview laboratory dataAssess and document complianceManage investigational productAssess, record, and report Adverse Events as outlined in the protocolManage/train ancillary staffQualifications
Education:
Experience and training in conducting clinical trials with knowledge of ICH GCPOR
Two years of college in a health-related program or LPNOR
Bachelor's degree in a health or scientific related programA thorough understanding of regulatory requirementsExcellent interpersonal and communication skills: Able to interact effectively with professional, administrative staff, sponsor and regulatory representatives, patients, potential subjects, and referral sources.Experience performing clinical assessments, including but not limited to obtaining vital signs, EKGs, blood draws, processing/shipping lab specimensExperience with CRIO (Clinical Trial Management System) is a plusExperience with administering vaccines is a plus
At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. We're an exceptional family of next-generation clinical trial sites, integrating cutting edge technology and high-quality support services, and significantly expanding participant engagement Founded in 2018, our company operates 18 clinical trial sites in the US and Canada with rapid plans for expansion.
The Role
Pharmasite, a Headlands Research site, is looking for a Clinical Research Coordinator to manage clinical research protocols. This individual will work directly with the investigators, and other research staff to ensure protocol visits are being conducted according to ICH GCP guidelines.
Responsibilities
Comprehend study design of each protocol that is assignedPerform procedures in compliance with the study protocolRecruit and screen study subjects according to specific protocol requirementsCollect and record study data in source documents via electronic system (CRIO)Manage study related activitiesAdherence to protocol requirementsReview laboratory dataAssess and document complianceManage investigational productAssess, record, and report Adverse Events as outlined in the protocolManage/train ancillary staffQualifications
Education:
Experience and training in conducting clinical trials with knowledge of ICH GCPOR
Two years of college in a health-related program or LPNOR
Bachelor's degree in a health or scientific related programA thorough understanding of regulatory requirementsExcellent interpersonal and communication skills: Able to interact effectively with professional, administrative staff, sponsor and regulatory representatives, patients, potential subjects, and referral sources.Experience performing clinical assessments, including but not limited to obtaining vital signs, EKGs, blood draws, processing/shipping lab specimensExperience with CRIO (Clinical Trial Management System) is a plusExperience with administering vaccines is a plus