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

This job is a great position for those continuing their career in clinical research and/or data management. The occupant will interact with patients, learn many relevant medical concepts pertaining to bleeding and clotting, and have opportunities to work in both clinical and laboratory projects, according to their interests and availability.
The successful applicant will work under the direct supervision of the Medical Directors and the general supervision of the Program Manager for the Massachusetts General Bleeding Disorders Center. They will support the management and operations of clinical and translational research projects. Duties include maintenance and retrieval of study data, implementation of study protocols, management with study regulatory matters.
The individual will also serve as a vital member of the Bleeding Disorders Center team responsible for coordination, integrity, and management of patient databases for the program. The successful applicant will serve as a liaison with national and regional study coordinating centers and with other participating treatment sites.
-Partner with aligned senior leaders to determine and plan for data analytics/reporting needs of a business unit or functional area(s).
-Mentor and train other data analysts.
-Identify trends, correlations, and anomalies in data and provide explanations or recommendations based on findings.
-Create clear, concise, and visually compelling data visualizations, dashboards, and reports.
-Present complex data and analytical findings in a meaningful and understandable manner to both technical and non-technical stakeholders.
-Performs comprehensive quality assurance, ensuring that data and reports meet end-user specifications and are accurate and reliable.

• Managing the HTC’s clinical research development processes from study start up to close out, including Institutional Review Board (IRB) submissions, third party grants/agreements submissions, and other regulatory matters.
• Maintaining the center’s American Thrombosis and Hemostasis Network (ATHN) database of our patient population in Clinical Manager, the Centers for Disease Control (CDC) repository for patient data collection required by the CDC.
• Provide back-up support for enrolling patients, conducting protocol related study visits, and data entry for studies conducted at the HTC
• Monitoring and reviewing data collection, entry, and other related activities to ensure protocol compliance and consistency
• Responsible for orienting and training new research staff on HTC research projects
• Maintaining regulatory documentation and site study files
• Manage study budgets, assisting with development of research budgets and reconciling payments for industry sponsored clinical trials.
• Coordinating activities at hospital to ensure correct testing/processing and send out instructions specific to the study
• Responsible for identifying new research projects, beneficial reports, and improving and streamlining research workflow
• Periodic testing of data validity, performing QA as well as identifying and resolving any errors or discrepancies.
• Responsible for completing annual reports as mandated by our HTC Region, ATHN/CDC, and Health and Human Services Administration (HRSA)
• Providing editorial support in designing and writing study protocols, designing study forms, and data reports.
• Conducting and coordinating qualitative/quantitative data analysis for projects as directed by medical directors and collaborating institutions.
• Maintain clear, accurate, and up to date records of patient study notes, including documentation of the informed consent process
• Conducting protocol related in-person/virtual visits with study participants. Completing, collecting, and tracking of all study forms.
• Assisting medical providers with organizing clinic visits, as needed, and identifying eligible patients for studies and the consent process.
• Attend monthly study site management meetings with sponsors
• Communicating project policies and procedures to personnel and third-party groups.
• Assisting with data gathering for other hemostasis and thrombosis related projects, such as surveys and patient reported outcomes.
• Pulling data and providing clean datasets to end users
• Participating in formal and informal presentations of protocols and results to staff. May also collaborate in preparing articles for journal publications and making presentations at conferences and meetings.
• Attending/conducting meetings, teleconferences, and webinars relevant to current or upcoming research and clinical projects
• Supports registration and updating of patient information on American Thrombosis and Hemostasis Network (ATHN) systems. Submitting surveillance data on demographics, bleeding, and clotting events of the MGH Hemophilia Treatment Center’s (HTC’s) patient population to ATHN and the CDC.
• Oversees the analyzing of HTC’s quality improvement transition project data
• Oversees the blood sample collection process for all patients enrolled in CDC/ATHN related research studies.
• Generating reports to end users
• Opportunities to participate in lab/bench work as needed

• Experience or familiarity with IRB processes
• Analytical skills to collect information from diverse sources, apply professional principles in performing various analyses, and summarize the information to solve problems.
• Excellent English language skills for writing, editing, and proofreading
• Excellent communication skills and sensitivity to confidentiality issues; diplomacy and discretion.
• Ability to handle multiple tasks simultaneously, prioritize, and meet deadlines.
• Ability to work collaboratively as part of a team
• Proficiency with multiple software applications, including Microsoft Office suite, database programs, and medical records programs such as EPIC.
• Healthcare experience, particularly in an academic setting is a plus
• Familiarity with EPIC and Data Management/Statistical software is a plus

Education

B.A., B.S. required. Individuals with other backgrounds with the requisite experience will be considered.

Experience

• Prior experience with data management and/or the IRB/clinical research process is preferred
• 3-5 years of experience in Academic/Research Environment

• Monday - Friday 9am to 5:30pm

• Onsite/Hybrid, 40 hours per week -will need to be on campus during Hemophilia/Bleeding Disorders clinics

• Location: Mass General Hospital - 55 Fruit Street, Boston MA

• This position does not support sponsorships for employment visa status? (e.g. H-1B Visa Status or OPT

Hybrid

32 Fruit Street

40

Regular

Day (United States of America)

Pay Range

$79,560.00 - $115,720.80/Annual

Grade

7

At 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.

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 Framework