Clinical Research Coordinator
Massachusetts General Hospital(MGH)

Boston, Massachusetts

This job has expired.


The MGH Cardiovascular Imaging Research Center has a unique blend of cardiology, cardiac imaging, and radiology researchers and interests with the goal to derive the most significant impact on patient health through collaborative research. We strive to be on the forefront of cardiovascular imaging research and to provide a collaborative forum for the medical community at large and the patients, researchers and clinicians with a specific interest in cardiovascular disease. We focus on contributing to bridging the gap between development of new imaging markers, novel medical therapies and proof their efficacy and efficiency in clinical practice. Our goal is to obtain a deeper understanding of interactions between different organ systems and how they affect cardiovascular health.

We have a faculty of 11, about 10 postdoctoral fellows and other support staff and collaborate with institutions nationally and internationally.

The MGH Cardiovascular Imaging Research Center is seeking a qualified individual to assist with and coordinate clinical research trials and observational studies. This position is front focused with a direct patient/participant contact. Additionally, scientific opportunities are available, encouraged and supported. We have a combined focus on the development of both the project and the applicant.

For this position, ongoing and planned multicenter trials are the focus. A specific focus of this position is on cardiovascular disease in patients with cancer. As background, there is an increase in rates of cardiovascular disease in patients who have cancer or who have been treated for cancer. Our understanding of this increase in cardiovascular disease in patients with cancer needs to improve. It is anticipated that this research area and these patients will be the focus of the current position.

We believe that this position would be an ideal step for an applicant who is considering careers in healthcare such as those applying to medical school, pharmacy school, and nursing school. However, we also believe that such a position would be suited to applicants who are considered long-term careers in clinical and imaging research.


Please note, the functions below are representative of major duties that are typically associated with these positions. Specific responsibilities may vary based upon departmental needs. Similarly, not all duties that have been outlined will be assigned to each position.

  • Collects & organizes patient data
  • Maintains records and databases
  • Uses software programs to generate graphs and reports
  • Assists with recruiting patients for clinical trials
  • Obtains patient study data from medical records, physicians, etc.
  • Conducts library searches
  • Verifies accuracy of study forms
  • Updates study forms per protocol
  • Documents patient visits and procedures
  • Assists with regulatory binders and QA/QC procedures
  • Assists with interviewing study subjects
  • Administers and scores questionnaires
  • Provides basic explanation of study and in some cases obtains informed consent from subjects
  • Performs study procedures, which may include phlebotomy.
  • Assists with study regulatory submissions
  • Writes consent forms
  • 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 recruitment strategies
  • Act as a study resource for patient and family
  • Monitor and evaluation lab and procedure data
  • Evaluate study questionnaires
  • Contribute to protocol recommendations
  • Assist with preparation of annual review
  • May assist PI to prepare complete study reports

  • Careful attention to details
  • Good organizational skills
  • Ability to follow directions
  • Good communication skills
  • Computer literacy
  • Working knowledge of clinical research protocols
  • Ability to demonstrate respect and professionalism for subjects' rights and individual needs
The Clinical Research Coordinator II should also possess:
  • Ability to work independently and as a team player
  • Analytical skills and ability to resolve technical problems
  • Ability to interpret acceptability of data results
  • Working knowledge of data management program

  • Bachelor's degree required.

  • 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.

  • A Clinical Research Coordinator I does not have any supervisory responsibility.
  • A Clinical Research Coordinator II may assist with the training and orientation of new staff members.

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.

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