Research Assistant, Addiction Psychiatry

BMC Software • Boston, MA

2d • $16 - $23 • Onsite

About The Position

The Research Assistant (RA) will support a new NIH-funded study, Ready 2 Respond: a randomized controlled trial (RCT) to evaluate the efficacy of a brief universal overdose prevention intervention in pediatric primary care. Health care providers will deliver an educational intervention to adolescents and young adults ages 13 to 26 on substance use safety information, including how to recognize and respond to an overdose, during routine appointments. Youth will be recruited from clinics across several Boston-area health centers. The study aims to address youth overdose risk by increasing youth knowledge on the risks of emerging drugs, such as illicit fentanyl, and better prepare youth to protect themselves and those around them from overdose. Conducts patient recruitment, administers questionnaires, abstracts medical records, maintains patient databases, performs administrative tasks, assists in grant preparation, performs literature searches and participates with the research team in preparation of data and other reports. May also assist the principal investigator with translation to Spanish, interpreting experimental results, and in preparing and writing manuscripts.

Requirements

• A minimum of a Bachelor’s degree is required by time of hire.
• Excellent English communication skills (oral and written).
• Cultural sensitivity and comfort with a wide range of social, racial and ethnic populations.
• Proficiency with Microsoft Office applications (i.e. MS Word, Excel, Access, PowerPoint, Outlook) and web browsers.
• Must be able to maintain strict confidentiality of all personal/health sensitive information.

Nice To Haves

• Experience in clinical research, public health experience or working with youth and families.
• Previous experience with recruiting subjects, with an understanding of the ethical and technical conduct of research.
• Bilingual candidate preferred, fluent in spoken and written English and Spanish.
• Experience with statistical software a plus.

Responsibilities

• Assists in data collection and provides feedback on study’s progress.
• Recruits subjects to participate in the study by using approved methodologies, such as, reaching to healthcare providers for referrals, visiting clinics, sending mailouts, using approved advertisements, etc.
• Conducts the enrollment of study participants, including explaining research procedures, and obtaining informed consent of subjects and/or their families.
• Schedules appointments of study participants; conducts reminder phone calls and/or sends mailouts.
• Obtains and distributes payment vouchers for participant reimbursements/participation.
• Responsible for the administrative aspects of the research study, including: managing program records and handling communication needs of the program.
• Prepares and maintains Institutional Review Board (IRB) approvals and correspondence, including amendments and renewals as necessary.
• Perform administrative duties associated with the study’s Data Monitoring and Safety Board, tracking and reporting adverse events and collecting data specified by the DSMB.
• Responsible for all other administrative duties related to research activities.

Benefits

• Competitive pay
• Tuition reimbursement and tuition remission programs
• Highly subsidized medical, dental, and vision insurance options
• 6.5 weeks of paid time off
• Career Advancement/Professional Development: Access a wealth of ongoing training and development opportunities that will not only enhance your skills but also expand your knowledge base especially for individuals pursuing careers in medicine or biomedical research.
• Pioneering Research: Engage in groundbreaking research projects that are driving the forefront of biomedical science.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level