Research Assistant I

Mass General Brigham•Brookline, MA

3d•$20 - $29•Hybrid

About The Position

Mass General Brigham relies on a wide range of professionals, including doctors, nurses, business people, tech experts, researchers, and systems analysts to advance our mission. As a not-for-profit, we support patient care, research, teaching, and community service, striving to provide exceptional care. We believe that high-performing teams drive groundbreaking medical discoveries and invite all applicants to join us and experience what it means to be part of Mass General Brigham. Job Summary Working closely with and under the supervision of the Project Manager and other study staff, provides support in the conduct of a NIHLBI funded Statin Therapy to Prevent Cancer Associated Venous Thromboembolism (STAT-CAT) in enrolling 4,000 participants across the US. We anticipate participants will be randomized over 8-10 sites throughout the US in a hospital or clinic setting where a physician or other qualified medical professional is present to evaluate the patient for inclusion and exclusion criteria. All trial follow-up will be conducted directly using electronic contact and/or call center telephone contact on a regular basis over the planned 12 month treatment period. After affirmation of participation into the trial, patients eligible for the treatment trial will have data registered into an electronic data system and will be randomized via a secure Internet Web-based Randomization System.

Requirements

B.A. or B.S.
Up to one year of experience in a medically related field or a research environment.
Ability to work independently.
Excellent interpersonal and telephone skills.
Excellent written and oral communication skills.
Excellent attention to detail.
Ability to prioritize a variety of tasks and appropriately seek guidance as needed.
High degree of computer literacy.
Sound independent judgment.

Nice To Haves

Spanish speaking preferred.
Fluent in Spanish.

Responsibilities

Supplying participants with study drug in child-proof bottles via overnight shipping directly to addresses as confirmed by the subject
Monthly follow-up calls to study participants to see how they are doing, have they been able to take the study pills, any side effects that they might have, any new medical conditions that have been diagnosed, new medications that they have started, and any other changes in their health
Participating in operational staff meetings, webinars, and Investigator teleconference calls and/or meetings
Assisting with maintaining contact with the randomized subjects, as needed.
Selecting the correct study drug box identified by a study randomization number assigned by the secure IWRS system and ship overnight using FedEx for next day delivery.
Following up to ensure receipt of assigned study medication or placebo within 48 hours of the shipment.
Assisting with inventory and acknowledge receipt of all study drug shipments and maintain accurate dispensing records.
Responding to study participants who need clarification of study protocol, methodology, and issues related to participation.
Forwarding calls to the appropriate staff, if unable to respond to the issue.
Documenting interactions with study participants by completing and processing the appropriate forms and entering summary information into electronic participant files.
Sharing responsibility for phone coverage to triage and respond to site queries, calls sites for missing forms or records, brings any issues or problems noted to supervisor for speedy resolution, and documents every phone conversation as appropriate.
Assisting with the preparation of medical records for endpoint adjudication by the physician endpoint committee.
Other duties as assigned.