Clinical Research Coordinator I (Clinical, Behavioral & Outcomes Research)

Joslin Diabetes Center•Boston, MA

9d•$22 - $24

About The Position

As a member of the clinical research team, the Clinical Research Coordinator I responsibilities will be associated with one or more clinical research project(s). In this role, you will work directly with patients with or without diabetes and chronic kidney disease and will assist with assigned study/studies. As a health care organization, we have the responsibility to do everything in our power to care for and protect our patients, our colleagues and our communities. We require that all staff be vaccinated against influenza (flu) as a condition of employment.

Requirements

Bachelor’s degree in the Biological Sciences/Chemistry or related science is required
Fluent in written and spoken English (additionally in Spanish is preferable)
Skilled user of Microsoft Office Suite
Ability to follow general instructions and procedures, as provided.
Strong interpersonal, organizational and communication skills (communicate clearly and effectively via verbal and written instruction).
Meticulous attention to detail
Professional and warm in demeanor, especially when relating to study participants and their families
Ability to maintain confidentiality
Ability to prioritize responsibilities – through completion.
Ability to work independently and with others in the team - to interact respectfully with other employees, professional staff and/or external contacts.
Excellent critical thinking and problem-solving abilities
Ability to learn sophisticated concepts and detailed protocols quickly

Nice To Haves

Previous research experience involving human subjects or clinical research preferred

Responsibilities

Provides support on clinical research protocols.
Recruits, schedules and interviews patients, performs routine laboratory procedures (including, measuring blood pressure, height and weight, and/or phlebotomy if certified) and protocol, and escorts patients to testing locations.
Coordinates patient recruitment to ensure the enrollment goals are met for multiple grants or industry sponsored clinical
Facilitates patient visits by performing protocol specific tests and procedures.
Assists with developing, maintaining and completing study data collection forms and source documents.
Maintains research patient records and regulatory binders.
Performs data entry.
Organizes the storage and use of the study related materials.
Participates in the labeling, organization, storage and retrieval and storage of study biospecimens.
Coordinates with Laboratory Cores for sample analysis.
Processes laboratory samples and deliver samples to local laboratory or mails to central laboratory.
Participates in the preparation of scientific publications and presentations of study scientific data.
Assists in training new team members in all clinical research protocols, including how to properly process and store samples.
Assists in keeping regulatory information up to date for the Joslin Internal Review Board (IRB) and the Committee on Human Studies (CHS).
Performs general laboratory support, including ordering supplies and equipment for all studies, and performing literature searches.
Activities for the studies will be performed at Joslin Diabetes Center and other facilities as required.
Will closely work with the staff involved in the study in and outside of Joslin Diabetes Center and under the supervision of the PI.
Participates in research team meetings including travel to Face to face steering committee meetings and study investigator meetings a few times a year.
Other duties as assigned.