Senior Clinical Research Coordinator

3 weeks ago

Somerville, Massachusetts, United States Massachusetts General Hospital(MGH) Full time

Job Summary:

The Massachusetts General Hospital (MGH) is seeking a highly skilled Senior Clinical Research Coordinator to lead a clinical research project on the natural history of Alternating Hemiplegia of Childhood. This is a unique opportunity to work on a cutting-edge project that involves the systematic collection of clinical data and biological specimens.

Key Responsibilities:

  • Conduct human subjects research following all ethical guidelines.
  • Establish data collection protocol.
  • Develop a written operations manual for the collection of data and biospecimens.
  • Conduct systematic neurologic exams on children with Alternating Hemiplegia of Childhood and their family members.
  • Collect blood, saliva, and urine samples from participants.
  • Supervise the proper handling and storage of biospecimens.
  • Supervise data entry and procedure for data verification and 'cleaning' (data quality control).
  • Analyze data and utilize results to improve on data collection protocol.
  • Present data at scientific meetings.
  • Write and edit manuscripts, serving as first author, for submission to neurology journals.

Qualifications:

  • Training in child neurology and movement disorder.
  • Training in clinical research methods.
  • Training in clinical operations, to facilitate the establishment of this program while working fairly independently.

Requirements:

  • Ability to handle sensitive and confidential matters discreetly and to ensure confidentiality guidelines are maintained by the team.
  • Ability to appropriately evaluate all aspects of a situation and to independently make appropriate and timely decisions.
  • Excellent interpersonal/communications skills and a good command of the English language, including medical and scientific terminology.
  • Exceptional computer skills (including operating systems, word processing, database, electronic mail, and Internet).
  • Knowledge in all aspects of laboratory safety and ability to ensure a safe environment for laboratory staff and subjects.

Education and Experience:

  • Bachelor's Degree required.
  • Minimum of 3-5 years of directly related experience.

Supervisory Responsibility:

  • The individual will supervise a clinical research coordinator, for approximately 50% of the coordinator's effort.

Working Conditions:

  • The work is performed via a combination of in-person research visits and internet-based research visits.
  • The work includes collection and handling of blood samples.
  • The work can be done in a hybrid manner, split between the office or clinic space and internet-based work.

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