Mass General Brigham
Employer Industry: Healthcare and Clinical Research
Why consider this job opportunity
Salary up to $28.44/hour
Opportunity for career advancement and growth within a well-respected healthcare organization
Flexible remote work environment
Comprehensive benefits package, including bonuses and recognition programs
Engaging and collaborative team culture focused on groundbreaking medical discoveries
Responsibilities
Enroll eligible patients in clinical research protocols and manage data collection for multiple cancer studies
Verify patient consent and eligibility criteria to ensure compliance with study protocols
Monitor patient participation and ensure protocol adherence through electronic medical record reviews
Prepare and submit regulatory documents to the Institutional Review Board (IRB)
Maintain communication with clinical teams and sponsors regarding study progress and patient data
Qualifications
Bachelor's Degree in a related field of study
1-2 years of research-related experience preferred
Strong attention to detail and good organizational skills
Ability to recognize compliance and data integrity issues
Effective communication skills with patients, vendors, and professional staff
Preferred Qualifications
Previous experience with clinical research protocols
Familiarity with regulatory requirements in clinical trials
Strong computer literacy and data management skills
Ability to demonstrate professionalism and respect for participant rights
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Why consider this job opportunity
Salary up to $28.44/hour
Opportunity for career advancement and growth within a well-respected healthcare organization
Flexible remote work environment
Comprehensive benefits package, including bonuses and recognition programs
Engaging and collaborative team culture focused on groundbreaking medical discoveries
Responsibilities
Enroll eligible patients in clinical research protocols and manage data collection for multiple cancer studies
Verify patient consent and eligibility criteria to ensure compliance with study protocols
Monitor patient participation and ensure protocol adherence through electronic medical record reviews
Prepare and submit regulatory documents to the Institutional Review Board (IRB)
Maintain communication with clinical teams and sponsors regarding study progress and patient data
Qualifications
Bachelor's Degree in a related field of study
1-2 years of research-related experience preferred
Strong attention to detail and good organizational skills
Ability to recognize compliance and data integrity issues
Effective communication skills with patients, vendors, and professional staff
Preferred Qualifications
Previous experience with clinical research protocols
Familiarity with regulatory requirements in clinical trials
Strong computer literacy and data management skills
Ability to demonstrate professionalism and respect for participant rights
#J-18808-Ljbffr