Clinical Research Coordinator NEUROLOGY KL

Site:
The Brigham and Women's Hospital, Inc.

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.

New budgeted research role

Job Summary

Summary

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.; maintaining and updating data generated by the study. Candidates who are in the process of completing their bachelor's degree have a grace period of six months from their hire date (up to 1 year if starting per diem) to provide degree equivalency verification.

We are looking for a hardworking, detail orientated, and focused candidate. Good interpersonal skills are required. The ideal candidate will be interested to grow in a long-term biomedical career in medicine or clinical research. Most time will be dedicated to clinical research activities, but there will be ample exposure to both clinical evaluation and basic science related to multiple system atrophy (MSA), Parkinson's disease, and other neurodegenerative disorders.

Wetlab procedures could include processing of patient samples for biobanking and culture of skin biopsy-derived fibroblasts. There is an opportunity for a collaborative project with neuroradiology involving image processing. There will be a requirement to keep detailed logs of patient research visits and research activities and liaise with regulatory staff for small-scale clinical trials. Interdisciplinary interactions will include physicians, scientists and allied health professionals.

There will be opportunity to contribute to scientific publications arising from this work.

Applications must include
1) cover letter;
2) biosketch, resume, or CV with GPA scores (or equivalent);
3) one letter of recommendation from a professional supervisor (e.g. advisor or previous PI); and
4) contact information for three supervisors who are willing to be contacted for reference. In addition to completing the online application, the complete application should be emailed to Dr. Daniel El Kodsi .

Does this position require Patient Care?

No

Essential Functions

* Assists research colleagues in the implementation, both internally and externally, of sponsored clinical research studies.

* Initiates and maintains contact with study participants.

* Responsible for screening applicants, ensuring they meet appropriate criteria, and making independent judgment as to the suitability of their participation.

* May be required to administer clinical tests such as smell tests, Montreal Cognitive Assessments, etc.

* There maybe opportunities to take history of patients, write up reports for attendings' review, and shadow on a weekly basis.

* Working in concert with Principal Investigator and/or Research Manager, develops and implements patient recruitment strategies.

* Develops, organizes, and/or maintains study databases, including a registry of patients tracked by the division. Responsible for data validation and quality control.

* In conjunction with Research Manager/Principal Investigator, develops and implements new research protocols including design, data collection systems and institutional review board approval.

* Recommends changes to research protocols.

* Performs literature searches, as appropriate.

* Assists PI or Research Manager with preparation for presentation and written published articles; there are opportunities to communicate research to colleagues.

* Responsible for training and orienting new staff.

* Reviews proposals for compliance with sponsor and organizational guidelines; verify all sponsor requirements are met.

* Recruiting patients for clinical trials, conducts 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.

* All other duties as assigned.

Qualifications

Education

Bachelor's Degree Science required

Experience

Some relevant research project work 0-1 year preferred

Qualifications

* Bachelor of Science degree in a biological science, or equivalent (e.g., pre-medical postbaccalaureate coursework).

* Prior experience in the clinic or clinical research is highly desired.

* Familiarity with research analysis

* At least one year of work experience in a research setting. Sound independent…