Clinical Research Coordinator bei Massgeneralbrigham
Massgeneralbrigham · Boston, Vereinigte Staaten Von Amerika · Onsite
- Junior
- Optionales Büro in Boston
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.
The scope of this research includes literature reviews, manuscript drafting, IRB preparation and submission, communications related to clinical and NJAM related research projects, maintaining and updating databases, data analysis, interview/focus groups, and abstract/manuscript preparation. This position will provide visibility and authorship on published manuscripts.
PRINCIPAL DUTIES AND RESPONSIBILITIES: Daily maintenance, management research database: · Data Collection and Chart Abstraction · Data Entry · Data Analysis · Preparation of Data Spreadsheets · Individual investigator assistance on database projects Clinical Duties: - MGH Site Clinical Coordinator for international, multi-institutional clinical studies - Coordinate prospective clinical studies in decision making. - Consent and register patients in the outpatient and inpatient settings for ongoing studies and trials. - Facilitate and obtain health quality of life questionnaires from patients with spine conditions. - Provide assistance researching and compiling manuscripts and abstracts. - Provide assistance with grant and protocol submissions and renewals. Administrative and Financial Duties: - Support the coordination of an extensive and ongoing international and domestic travel schedule including planning all travel-related activities, conducting necessary research, providing documentation, and creating detailed itineraries. - Process financial transactions according to MGB guidelines and procedures, including reimbursements, corporate cards expenditures, and purchasing.
Preferred Skills: Experience in medical, ethics, and/or legal research and participant interactions strongly preferred. Comfortable working with a diverse population and interacting with medical personnel. The ability to work independently. Handle confidential and sensitive information with care. Familiarity with research methods, study design, and evaluation. Strong analytical skills. Computer research skills in programs such as Excel, PowerPoint, Word, Photoshop, and Adobe are critical. Familiarity with redcap is essential. Excellent communication, organizational skills, and attention to detail are essential. Requires the ability to take initiative and troubleshoot. EXPERIENCE: experience related to neurotechnology preferred.
Job Summary
Job Profile SummarySummary
Following established policies, procedures, and study protocols, provides assistance on clinical research studies, including recruiting, evaluating, and consenting patients for studies; collecting and organizing patient data; scheduling patients for study visits; performing clinical tests such as phlebotomy, EKGs, etc.; and maintaining and updating data generated by the study. Candidates who are in the process of completing their bachelor's degree have a six-month grace period from their hire date (up to one year if starting on a per diem basis) to provide degree equivalency verification.
Does this position require Patient Care?
No
Essential Functions
-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.
Qualifications
Bachelor's Degree Related Field of Study required
Can this role accept experience in lieu of a degree?
Yes
Licenses and Credentials
Experience
Some relevant research project work 0-1 year preferred
Knowledge, Skills and Abilities
- Careful attention to detail and good organizational skills.
- Ability to follow directions.
- Good interpersonal and communication skills.
- Computer literacy.
- Working knowledge of clinical research protocols.
- Ability to demonstrate respect and professionalism for subjects' rights and individual needs.
Additional Job Details (if applicable)
Remote Type
Work Location
Scheduled Weekly Hours
Employee Type
Work Shift
Pay Range
- /
Grade
5
EEO Statement:
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.
