***The CRC must be fluent in English and Spanish.***
The Natarajan Lab seeks a highly motivated and experienced individual for a Clinical Research Coordinator (CRC) I position to assist with ongoing and future clinical research studies. The CRC I will work closely with the lab's clinical research team on managing and executing cardiovascular disease, community health, and genomics projects.
The CRC I must be able to multi-task in a dynamic clinical research setting. This position works closely with the study team, including study physicians, nurses, and cardiology administration, and involves significant patient contact. The ability to work well in a team is a must. The flexibility to work independently is also necessary. This is the ideal position for someone looking to work with a dedicated group of people and get involved in clinical trials. The CRC I will gain invaluable experience in the field of cardiology in an academic clinical and community-based research setting.
This is a full-time (40 hours/week) onsite position, and fluency in Spanish is required.
This position is ideal for someone interested in pursuing graduate studies or a career in the fields of medicine, public health, or clinical research. It involves patient interaction as a member of a clinical research team. Administrative responsibilities are also required of the individual who fills this role.
PRINCIPAL DUTIES AND RESPONSIBILITIES:
***The CRC must be fluent in English and Spanish.***
The Clinical Research Coordinator I has the following duties and responsibilities:
Manages trials under the supervision of the PI, working towards independent execution of clinical and community-based trials
Assess eligibility for studies
Manages subject recruitment, assesses eligibility for studies including pre-screening and follow-up calls
Conducts and documents informed consent process
Coordinates and conducts research study visits. Will be required to perform clinical tests such as vital signs, etc. (Training will be provided.)
Tracks individual subject participation in research study
Maintains study regulatory binder, including screening and enrollment logs
Obtains, enters, and maintains research data, patient files, and study databases
Links research activities related to study protocols to patients in EPIC, including ordering study medications and scheduling research study visits
Prepares invoices; utilizes Epic to schedule patients for study visits, and verify patient care charges as appropriate to study funds and/or insurance
Acts as study resource for patient and family
Manages all Institutional Review Board (IRB) documentation accurately. Drafts and submits applications to the IRB, including initial submissions, amendments, and continuing review
Prepares documents and study binders for FDA audits (if needed)
Orients and trains junior team members on the study protocols as appropriate
Maintains a good understanding of the study protocols and study start-up/closeout process
Assists with other research-related administrative tasks as needed
Conducts outreach and engagement activities that support patient continuity of care
Handle and protect confidential and sensitive data with integrity
Attend all team and study-related meetings
Qualifications
SKILLS/ABILITIES/COMPETENCIES REQUIRED:
***The CRC must be fluent in English and Spanish.***
The Clinical Research Coordinator I should have the following skills and competencies:
High degree of computer literacy including Microsoft Excel, Word, PowerPoint, and Outlook programs; ability to learn new software (Epic, REDCap, PeopleSoft, etc.)
Ability to work independently and as a team member
Analytical skills and ability to resolve technical problems
Ability to multi-task and prioritize responsibilities
Basic laboratory techniques and methods
Excellent patient communication skills
Phlebotomy training (or willingness to become trained in phlebotomy)
Exceptional organizational skills and the flexibility to handle multiple tasks and deadline pressures
Fluency in Spanish is required.
Any coding or computational science experience is a plus, but not required
EDUCATION:
Minimum education required BA/BS (preferred in science related field). MS or MPH is a plus but not required.
EXPERIENCE:
Previous experience in clinical research is a plus. Past experience in coursework involving laboratory skills, as well as past experience in a hospital setting, is strongly encouraged. Some familiarity with medical terminology is needed. Past patient-facing clinical experience is strongly encouraged.
Prior experience in clinical research, including community-based research and/or industry-sponsored investigational new drugs, is a plus but not required.
SUPERVISORY RESPONSIBILITY:
None.
FISCAL RESPONSIBILITY:
May monitor and manage study funds. Responsible for preparing invoices and for directing, verifying, and correcting patient care charges as appropriate. These may be industry sponsor funds or NIH grants.
WORKING CONDITIONS:
Duties will be performed in an office, community-based organizations (CBOs) such as businesses, barbershops and churches, and hospital setting (outpatient cardiology clinics).
EEO Statement
Massachusetts General Hospital is an Equal Opportunity Employer. By embracing diverse skills, perspectives and ideas, we choose to lead. Applications from protected veterans and individuals with disabilities are strongly encouraged.
