Clinical Research Coordinator Bilingual in English and Spanish
Mass General Brigham
- Boston, MA Nashua, NH
- Permanent
- Full-time
- Assists with developing and implementing recruitment and retention strategies.
- Verifies subject inclusion/exclusion criteria, and collects informed consent and research data from study participants carefully following protocols and scripts.
- Describes research study to patients and answers questions.
- Manages mailings and distribution of study related materials, such as recruitment letters and study incentives.
- Assists in coordinating the schedule of participant contacts and activities throughout the study.
- Responsible for data collection, preparing reports, and providing feedback on process improvement.
- Completes all necessary paperwork and data documentation, including coding and cleaning data forms, and assists with QA/QC data checks.
- Prepares data for analysis and data entry, and assists with formal audits of data.
- Provides data management, coordination, and patient/participant outreach as needed.
- Contributes to a positive experience for research participants through courteous telephone, email, and in-person interactions.
- Schedule, set agendas, attend, and create minutes for study team meetings
- Works as an effective program team member. Contributes to the teamwork within and between departments. Regularly attends and participates in meetings. Provides constructive ideas, suggestions and feedback in a positive manner. Works collaboratively.
- Other duties as assigned.
- Careful attention to details
- Good organizational, time management, and communication skills
- Ability to follow directions
- Ability to build trust and maintain confidentiality with diverse populations, including health center providers, staff, patients, and research participants
- Ability to identify and follow through on project issues and use initiative
- Computer literacy, including word processing, database, and spreadsheet software
- Working knowledge of clinical research protocols
- Ability to demonstrate respect and professionalism for subjects' rights and individual needs
- Ability to handle confidential and sensitive information discreetly
- Good interpersonal skills, including written and verbal communication
- Bilingual in English and Spanish strongly preferred
- 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.