Req#: R34327
Category(s): Research, Research Support
Full Time / Part Time: Full-Time
Shift: First
Location: 3601 Main Street Springfield MA (HYBRID WORK OPPORTUNITY)
Dr. Peacock-Chambers is looking to hire a Research Assistant to join her team and participate in federally funded cutting edge research to support parental mental health. She is currently hiring for an NIH-funded clinical trial. The "Mothering from the Inside Out" (MIO) trial (R01DA058125) will test the implementation and effectiveness of MIO when delivered by substance use treatment counselors in Springfield, Holyoke, and Worcester.
This position seeks a candidate with a willingness to take on new challenges and possessing excellent organizational and critical thinking skills. This position will be primarily responsible for recruitment of study subjects (women in recovery with children age 0-5 years) during in-person visits to substance use treatment clinics in Worcester, Holyoke, and Springfield approximately 4 days per week. In addition, the position requires video/phone follow-up for data collection. This position will also support data analysis activities and require some administrative duties including: meeting coordination and other administrative tasks as needed throughout the course of employment. This position is grant funded for the next 4+ years.
Job Responsibilities:1) Assists with moderately complex study tasks in accordance with protocol guidelines.
2) Performs Level I responsibilities with a higher level of problem resolution, analytical ability and self-direction.
3) May have other responsibilities including maintenance of inventory/ordering of study supplies, scheduling of study meetings, budget tracking, etc.
4) Contributes to preparation, submission, and maintenance of regulatory documents.
5) Performs actual study tasks as directed.
6) Accurately compiles information and data.
7) May assist with sponsor/CRO visits.
8) Adheres to protocol, IRB, HIPAA, and regulatory requirements.
9) Under the direction of the study coordinator or principal investigator, assist in enrolling patients in research studies. Contact patients as required after initial contact to obtain additional information.
10) Order and maintain a log of stipend checks and/or gift certificates to be distributed to study participants.
Required Work Experience:1) Bachelors, in basic sciences, public health, psychology, sociology, etc.
Preferred Work Experience:1) 2+ years clinical research experience
Skills and Competencies:Seeks/completes additional research education and training.
Human Subjects Protection training (CITI) and any additional training as specified by the IRB prior to beginning any actual work on research protocols.
Knowledge of data utilization, complex problem solving, critical thinking, resource management, and writing skills.
Solid Computer Skills, including Databases.
A basic understanding of data collection and research principles is preferred.
May possess working knowledge of State & Federal Regulations as they relate to research.
Highly detail-oriented individual with excellent interpersonal and time management skills.
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At Baystate Health we know that treating one another with dignity and equity is what elevates respect for our patients and staff. It makes us not just an organization, but also a community where you belong. It is how we advance the care and enhance the lives of all people.
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Education:
Bachelors Degree (Required)
Certifications:
Human Subjects Research – CITI ProgramCITI Program
Equal Employment Opportunity Employer
Baystate Health is an Equal Opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, marital status, national origin, ancestry, age, genetic information, disability, or protected veteran status.
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