Mass General Brigham→
Clinical Research Coordinator - Albers… at Mass General… · Charlesto…
Entry LevelOn-siteFull-timeCharlestown-MA$42k–$60k/yr
Skills
clinical research studiespatient recruitmentphlebotomyekgdata collectiondata analysisregulatory submissionscentral irb protocolsneurological disease researcholfactory function assaysstatistical data presentation
Job Description
Summary: Mass General Brigham is a not-for-profit organization focused on advancing patient care, research, teaching, and community service. The Clinical Research Coordinator will assist in clinical research studies by recruiting and evaluating patients, collecting data, and performing clinical tests while ensuring compliance with protocols and regulatory requirements.
Responsibilities:
- Reviews proposals for compliance with sponsor and organizational guidelines; verifies that all sponsor requirements are met
- Recruiting patients for clinical trials and conducting phone interviews
- Verifies the accuracy of study forms and updates them per protocol
- Prepares data for analysis and data entry
- Documents patient visits and procedures
- Assists with regulatory binders and QA/QC Procedures
- Assists with interviewing study subjects
- Assists with study regulator submissions
Required Qualifications:
- Bachelor's degree or in the process of completing a bachelor's degree with a six-month grace period to provide degree equivalency verification
- Experience with central IRB protocols is strongly preferred
- Ability to assist on clinical research studies, including recruiting, evaluating, and consenting patients for studies
- Ability to collect and organize patient data
- Ability to schedule patients for study visits
- Ability to perform clinical tests such as phlebotomy, EKGs, etc
- Ability to maintain and update data generated by the study
- Ability to review proposals for compliance with sponsor and organizational guidelines
- Ability to verify the accuracy of study forms and update them per protocol
- Ability to prepare data for analysis and data entry
- Ability to document patient visits and procedures
- Ability to assist with regulatory binders and QA/QC Procedures
- Ability to assist with interviewing study subjects
- Ability to assist with study regulator submissions
Required Skills: Clinical Research Studies, Patient Recruitment, Phlebotomy, EKG, Data Collection, Data Analysis, Regulatory Submissions, Central IRB Protocols, Neurological Disease Research, Olfactory Function Assays, Statistical Data Presentation
Benefits: Comprehensive benefits, Career advancement opportunities, Differentials, Premiums, Bonuses, Recognition programs designed to celebrate your contributions and support your professional growth
Benefits
Comprehensive benefits
Career advancement opportunities
Differentials
Premiums
Bonuses
Recognition programs designed to celebrate your contributions and support your professional growth