Clinical Research Associate

Mass General Brigham; Boston (MA); Hybrid; USD 28,000 - 40,000; Full time

Job summary

Mass General Brigham in Boston seeks a Clinical Research Associate to ensure regulatory requirements for clinical trials are met. You will work with IRBs, sponsors, and federal agencies, and support the trial lifecycle with documentation and reporting.

The role requires a Bachelor’s degree and attention to detail, with hybrid work options and ongoing training in institutional and federal regulations governing clinical research.

Qualifications

• Bachelor's degree required with knowledge of clinical trial processes.
• Ability to recognize compliance and data integrity issues.
• Understanding of IRB processes and federal regulations.

Responsibilities

• Maintain and organize study-specific regulatory binders.
• Prepare protocol amendments, continuing reviews, and safety reports to IRB.
• Revise informed consent documents with new risk information.
• Collect, complete, and submit essential regulatory documents to regulatory entities.

Skills

Attention to detail

Regulatory compliance

Communication skills

Knowledge of clinical research

Education

Bachelor's Degree

Job description

Site: The General Hospital CorporationMass General Brigham relies on a wide range of professionals, including doctors, nurses, business people, tech experts, researchers, and systems analysts to advance our mission. As a not-for-profit, we support patient care, research, teaching, and community service, striving to provide exceptional care. We believe that high-performing teams drive groundbreaking medical discoveries and invite all applicants to join us and experience what it means to be part of Mass General Brigham.Job SummaryWorks under general supervision to ensure the regulatory requirements for clinical trials are met. This position involves working with clinical teams, Institutional Review Boards (IRB), clinical trial sponsors, and federal regulatory agencies. The Clinical Research Associate will be trained on the institutional and federal regulations governing clinical research.Does this position require Patient Care?- NoEssential Functions- Maintain and organize study-specific regulatory binders.- Prepare and submit protocol amendments, continuing reviews, and safety reports to the IRB.- Revise informed consent documents to include new risk information and/or updated protocol requirements through the course of the study.- Manage adverse event and deviation/violation/exception documentation for all enrolled patients and report to the sponsor and IRB as required.- Maintain source documentation of correspondence with the IRB, investigators, and sponsors throughout the clinical trial process.- Collect, complete, and submit essential regulatory documents to various regulatory entities.- Participate in monitoring visits and maintain a record of all correspondence related to these visits.QualificationsBachelor's Degree requiredResearch Experience 1-2 years preferredKnowledge, Skills and Abilities- Attention to detail.- Ability to recognize compliance and data integrity issues and respond appropriately.- Working knowledge of clinical research protocols.- Ability to communicate effectively with patients, vendors, contract research organizations and professional staff.- Effective interpersonal and communication skills.Additional Job Details (if applicable)Remote TypeHybridWork Location101 Merrimac StreetPay Range$20.16 - $29.01/HourlyGrade5At Mass General Brigham, we believe in recognizing and rewarding the unique value each team member brings to our organization. Our approach to determining base pay is comprehensive, and any offer extended will take into account your skills, relevant experience if applicable, education, certifications and other essential factors. The base pay information provided offers an estimate based on the minimum job qualifications; however, it does not encompass all elements contributing to your total compensation package. In addition to competitive base pay, we offer comprehensive benefits, career advancement opportunities, differentials, premiums and bonuses as applicable and recognition programs designed to celebrate your contributions and support your professional growth. We invite you to apply, and our Talent Acquisition team will provide an overview of your potential compensation and benefits package.EEO Statement:1200 The General Hospital Corporation is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religious creed, national origin, sex, age, gender identity, disability, sexual orientation, military service, genetic information, and/or other status protected under law. We will ensure that all individuals with a disability are provided a reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. To ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Veteran’s Readjustment Act of 1974, and Title I of the Americans with Disabilities Act of 1990, applicants who require accommodation in the job application process may contact Human Resources at (857)-282-7642.Mass General Brigham Competency FrameworkAt Mass General Brigham, our competency framework defines what effective leadership “looks like” by specifying which behaviors are most critical for successful performance at each job level. The framework is comprised of ten competencies (half People-Focused, half Performance-Focused) and are defined by observable and measurable skills and behaviors that contribute to workplace effectiveness and career success. These competencies are used to evaluate performance, make hiring decisions, identify development needs, mobilize employees across our system, and establish a strong talent pipeline.