System One
Title:
Drug Clinical Research Coordinator
Location:
Boston, MA
Schedule:
M-F (onsite daily) 8-5
Duration:
6 month contract to hire
Pay Rate:
$25-$30/hr
Start:
ASAP
Education • Bachelor’s Degree
Requirements
1-3 years of relevant experience in human clinical trial research, with cardiovascular disease experience preferred
Knowledge of federal and institutional policies governing human clinical research
Proficiency with PCs and windows-based software, including Word, Excel and data management system
Be fluent in English and Spanish (preferred)
Strong organizational skills with ability to multi-task
Possess good judgment skills with ability to interpret information and protocol requirements, and initiate appropriate actions
Assist Sr. Project Manager with documentation and follow up paperwork for the trial
Accomplished documentation skills with meticulous attention to detail
Ability to complete tasks with aggressive deadlines and competing priorities
Comfortable with hospital in-patient and out-patient environments
Responsibilities
Assist Sr. Project Manager and team members with all phases of clinical research to include: Trial Initiation, Trial Coordination/Implementation/Maintenance, and Trial Close-out
Assist in development of trial protocol IRB application and submit to appropriate authority; Assist in the preparation and/or review budgets, coordinate and work with ancillary departments/services as needed to successfully execute protocol elements; assist in the plan for site initiation once IRB protocol approval is received
Working with a PA, conduct medical record screening of cardiovascular in-patients and out-patients to identify eligible potential trial subjects; be prepared to approach potential subjects, and/or family members with trial specific information for review/consideration; assist in the recruitment of qualified/interested trial participants
Assist in maintaining accurate case report forms, regulatory binders, and meticulous trial records; schedule and conduct follow-up trial visits
Obtain and process biological samples according to protocol (after completing any necessary training)
Assist with preparation and submission of final trial report to the IRB for review
Assist in the preparation of all documents/files/binders/electronic data for sponsor-initiated or FDA audits
#J-18808-Ljbffr
Drug Clinical Research Coordinator
Location:
Boston, MA
Schedule:
M-F (onsite daily) 8-5
Duration:
6 month contract to hire
Pay Rate:
$25-$30/hr
Start:
ASAP
Education • Bachelor’s Degree
Requirements
1-3 years of relevant experience in human clinical trial research, with cardiovascular disease experience preferred
Knowledge of federal and institutional policies governing human clinical research
Proficiency with PCs and windows-based software, including Word, Excel and data management system
Be fluent in English and Spanish (preferred)
Strong organizational skills with ability to multi-task
Possess good judgment skills with ability to interpret information and protocol requirements, and initiate appropriate actions
Assist Sr. Project Manager with documentation and follow up paperwork for the trial
Accomplished documentation skills with meticulous attention to detail
Ability to complete tasks with aggressive deadlines and competing priorities
Comfortable with hospital in-patient and out-patient environments
Responsibilities
Assist Sr. Project Manager and team members with all phases of clinical research to include: Trial Initiation, Trial Coordination/Implementation/Maintenance, and Trial Close-out
Assist in development of trial protocol IRB application and submit to appropriate authority; Assist in the preparation and/or review budgets, coordinate and work with ancillary departments/services as needed to successfully execute protocol elements; assist in the plan for site initiation once IRB protocol approval is received
Working with a PA, conduct medical record screening of cardiovascular in-patients and out-patients to identify eligible potential trial subjects; be prepared to approach potential subjects, and/or family members with trial specific information for review/consideration; assist in the recruitment of qualified/interested trial participants
Assist in maintaining accurate case report forms, regulatory binders, and meticulous trial records; schedule and conduct follow-up trial visits
Obtain and process biological samples according to protocol (after completing any necessary training)
Assist with preparation and submission of final trial report to the IRB for review
Assist in the preparation of all documents/files/binders/electronic data for sponsor-initiated or FDA audits
#J-18808-Ljbffr