drjobs Clinical Rsch Coord Sr

Clinical Rsch Coord Sr

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1 Vacancy
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Job Location drjobs

Boston - USA

Monthly Salary drjobs

Not Disclosed

drjobs

Salary Not Disclosed

Vacancy

1 Vacancy

Job Description

Qualifications
A bachelors degree is required. A masters in public health psychology clinical research administration or related field is preferred.
A minimum of three years of relevant research experience or a combination of relevant research and administrative experience is required.
Senior Research Coordinator
General Overview
The Massachusetts General Hospital Center for Womens Mental Health is dedicated to the evaluation and treatment of psychiatric disorders associated with female reproductive function. The Center provides consultation to women regarding the use of psychiatric medications during pregnancy and treatment for postpartum mood and anxiety disorders. The Center also treats women with premenstrual dysphoric disorder and menopause related mood and anxiety disorders. For more information about the clinical and research program please visit our website at www.womensmentalhealth.
Reporting to and working closely with the Director the Senior Research Coordinator will be responsible for the coordination and management of the Centers portfolio of clinical research studies under the guidance of the principal investigators. Additionally the Sr. Research Coordinator will be responsible for coordinating grant submissions financial oversight and other Centerwide administrative and regulatory activities.
This is a challenging position ideal for someone who enjoys multitasking problem solving and project management. The Sr. Research Coordinator plays a significant part in guiding the research activities of the Center and fulfilling its clinical and research missions. In this role a successful employee will develop a broad set of skills in financial management grant writing and project management which will situate them to advance into research management and other higherlevel management positions.
Responsibilities
Responsibilities include but are not limited to:
Study Coordination
  • Coordinating an active clinical research portfolio including a range of human subjects studies and related clinical research activities including recruitment IRB oversight regulatory matters and manuscript preparation
  • Providing oversight for all research activities
  • Serving as a study resource for patients and families
Grant Management
  • Working with PIs to develop budgets and coordinate all aspects of grant submission to federal industry and foundation funding agencies
Financial Administration
  • Primary point of contact for the Office of Research Management Office of Research Finance Office of Development and the Departments Senior Grants Administrator.
Other Responsibilities
  • Quality control: Develop systems for QA/QC performing QA/QC checks
  • Supervise staff as assigned including the training and evaluation of new staff
Skills/Abilities/Competencies
  • Thrive in a busy work environment that requires coordination of multiple activities and the judgment and flexibility to reprioritize to accommodate emergency requests
  • Function independently and work with only very general direction from the Director
  • Make independent and effective decisions
  • Independently prioritize tasks and set deadlines
  • High level organizational and time management skills
  • Sound interpersonal skills and the ability to effectively train and supervise others
  • Ability to work well as a member of a team
  • Handle sensitive and confidential issues
  • Strong analytical skills to problem solve efficiently
  • Strong database management and computer proficiency and ability to learn new computer programs quickly
  • Ability to display initiative and introduce innovations to active research projects
Working Environment
Currently our group is made up of four research coordinators a senior research coordinator a program assistant and eight psychiatrists two of whom are principal investigators including the Director. The senior research coordinator works closely with the principal investigators program assistant and research coordinators and the group meets twice weekly to review study progress and once a week to review clinical cases. There is flexibility for this to be a parttime position or fulltime position depending on availability. The workday will be within the framework of a 9:005:30 workday and a hour unpaid lunch. Our Center is located in the Simches Research Building in a combined administrative and clinical space and all work is conducted onsite.

Employment Type

Full Time

Company Industry

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