Job Description:

GENERAL SUMMARY/ OVERVIEW STATEMENT:


The Psychiatric and Neurodevelopmental Genetics Unit (PNGU) of the Massachusetts General Hospital (MGH) has an immediate opening for a Clinical Research Coordinator, working under the direction of Dr. Alexandre Lussier. Dr. Lussier's research laboratory is housed in the Center for Genomic Medicine and Department of Psychiatry. Research in the Lussier Lab is focused on identifying the social and biological determinants of mental health through studies on (1) the impact of early-life stressors, such as prenatal alcohol exposure and childhood adversity, on trajectories of mental health and resilience; (2) genomic and epigenomic predictors of psychopathology; and (3) gene-environment interactions, or how genetic mechanisms modify the effects of life experiences on risk for mental illness across the lifespan.


The Lussier lab is a highly collaborative research team that leverages large-scale human data and interdisciplinary approaches to investigate when and how early-life environments influence mental health, with the ultimate goal of identifying ways to predict and prevent mental illness. We at the Lussier lab firmly believe that this goal, and science in general, is strengthened by the inclusion of diverse voices and perspectives. We recognize that diversity manifests in many different ways, including differences in background, life experiences, training, etc. As such, we encourage candidates from underrepresented backgrounds to work with us.


The Lussier lab is seeking a Clinical Research Coordinator I or II to assist with translational research projects, as well as perform administrative tasks to support the day-to-day operations of the lab. Responsibilities will include: conducting literature searches, participating in data management and data analysis tasks, helping with grant and peer-reviewed journal submissions, developing materials for conference presentations, and performing other administrative support duties as required. Candidates must have a BA/BS, 1-2 years of experience, good quantitative skills, an ability to work well in a collaborative environment, fluency with all modes of communication in English, and strong writing skills.


Candidates will gain valuable experience and knowledge working in all phases of the research process, ranging from study design to the analysis and interpretation of results. Opportunities to co-author manuscripts and present study results at conferences may be available. Finally, candidates will have the opportunity collaborate with world-class researchers at MGH, Harvard, and beyond, and will closely interact with members the Dunn lab in the PNGU. This position is ideal if you wish to pursue graduate studies in public health, psychology, or medicine.


PRINCIPAL DUTIES AND RESPONSIBILITIES:

• Collects & organizes data from large-scale epidemiology studies


• Maintains records and databases


• Uses software programs to generate graphs and reports


• Obtains study data from birth cohorts, medical records, physicians, etc.


• Conducts library searches


• Verifies accuracy of study forms


• Assists with regulatory binders and QA/QC procedures


• Performs study procedures


• Assists with study regulatory submissions (e.g., IRB submissions)


• Aids with the preparation of manuscript submissions and conference presentations


• Verifies subject inclusion/exclusion criteria


• Performs administrative support duties as required

A Clinical Research Coordinator II performs the duties of a Clinical Research Coordinator I (above) and may also:

• Maintain research data, patient fields, regulatory binders and study databases


• Perform data analysis and QA/QC data checks


• Organize and interpret data


• Develop and implement strategies for public and patient involvement


• Monitor and evaluate lab and procedure data


• Evaluate study questionnaires


• Contribute to protocol recommendations


• Assist with preparation of annual review


• Help PI prepare complete study reports, including conference abstracts and manuscripts

SKILLS/ABILITIES/COMPETENCIES REQUIRED:


• Careful attention to details


• Good organizational skills


• Ability to follow directions


• Good communication skills


• High degree of computer literacy


• Analytical skills and ability to resolve technical problems


• Working knowledge of clinical research protocols


• Ability to demonstrate respect and professionalism for subjects' rights and individual needs


• Ability to work independently and as a team member


• Ability to interpret acceptability of data and results



Qualifications

EDUCATION:


BA/BS Required


EXPERIENCE:


New graduates with some relevant course/project work or those without any prior research experience will be considered for the Clinical Research Coordinator I position outlined above.


Those with a minimum of 1-2 years of directly related work experience will be considered for a Clinical Research Coordinator II position.


SUPERVISORY RESPONSIBILITY (if applicable):


May assist with the training and orientation of new staff members.


WORKING CONDITIONS:


Remote, Laboratory and Office Settings



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. Apply Now