Clinical Research Coordinator Job at Mass General Brigham, Boston, MA

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  • Mass General Brigham
  • Boston, MA

Job Description

Site: The General Hospital Corporation

Mass 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 Summary
The selected candidate will work independently to coordinate clinical research projects under the direct supervision of the principal investigators, and with the support of an established team of clinical research coordinators. The candidate will be responsible for all study tasks related to Pancreatic diseases including, but not limited to various forms of pancreatitis, pancreatic cysts, and possibly pancreatic cancer. The candidate will work with members from both the gastroenterology and surgical teams along with other members of the multidisciplinary clinical and research team.

The candidate will work full time (40 hours/week) however the schedule will require flexibility and may include occasional evenings depending on time-management and patient schedules. The research studies will continue for approximately 2 years or more. This research environment is highly conducive to individuals interested in eventually pursing medical, graduate, or public health advanced degrees. There will be mentored opportunities for publication and presentation depending on the candidate's interest.

This position offers the opportunity to work directly with patients and physicians, and it will provide foundational skills in conducting clinical research in a large, academic medical center.

Qualifications

Primary Responsibilities
  • Recruit and enroll eligible study participants from clinics throughout the hospital
  • Arrange and conduct initial interviews of study subjects and evaluate criteria for inclusion/exclusion
  • Take subject vital signs; draw blood samples and perform sample processing
  • Perform Institutional Review Board (IRB) submission process by preparing protocol applications, amendments, safety reports, adverse event reports and other documents
  • Capture clinical information from record review and patient interview into study database
  • Perform bio-specimen processing, aliquoting, tracking and shipping
  • Keep bio-specimen electronic and physical inventories current and available
  • Manage and maintain regulatory documents for audit by FDA, as needed
  • Prepare and manage regulatory documents for audit by FDA, as needed
  • Act as primary study resource for laboratory staff, patients and families
  • Evaluate and update medical records and maintain study database
  • Coordinate subject care by scheduling and arranging follow-up visits, conducting follow-up telephone calls, and communicating concerns with the study investigator
  • Conduct regular review of study progress and follow-up
  • Attend weekly coordinator meetings, and prepare weekly reports of work performed

Skills/Abilities/Competencies Required
  • Excellent interpersonal, verbal and written communication skills in English
  • Ability to manage time effectively
  • Ability to work independently and as a collaborative team member
  • Ability to maintain accurate records
  • Ability to organize, analyze, summarize, and present data
  • Experience in a clinical environment or biobanking preferred
  • Experience and proficiency in biospecimen (blood, stool, tissue, urine) handling preferred, but not required

Education

B.A./B.S. degree required

B.A./B.S. minimum 1-year experience is required for CRC II position

Experience
  • Background in biology, immunology, biochemistry, biostatistics, epidemiology or related pre-medicine discipline preferred, but not required
  • Experience in a clinical research environment or with specimen biobanking preferred

Additional Job Details (if applicable)

Remote Type

Onsite

Work Location

125 Nashua Street

Scheduled Weekly Hours

40

Employee Type

Regular

Work Shift

Day (United States of America)

EEO Statement:

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 [click to reveal phone number](857)-282-7642 .

Mass General Brigham Competency Framework

At 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.

Job Tags

Full time, Shift work, Afternoon shift,

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