A Research Assistant I position is currently available in Dr. Kent Kiehl’s laboratory at The Mind Research Network in Albuquerque, New Mexico. Duties include working with a research team on several grant funded studies grant-funded studies designed to evaluate neurobehavioral characteristics of incarcerated criminal offenders with antisocial (e.g., psychopathic) traits, substance use disorders, and/or past traumatic events (including traumatic brain injury). Our studies also investigate the impact of treatment (e.g., mindfulness, cognitive skills training) as well long-term outcomes post-release from incarceration. The RAI will assist with recruiting, scheduling, and screening study participants, file scanning, data entry, and various data management projects (coding, scoring, etc). Depending on interests and experience, training may also be provided in in the administration and scoring of clinical interviews and neuropsychological tests, and/or collecting/analyzing brain imaging (e.g., functional magnetic resonance imaging (fMRI)) data. All candidates should possess strong interest in research with incarcerated populations.

Qualifications

Requires a high school diploma or equivalent and 2 years of relevant experience; or an equivalent combination of education, training and/or experience from which comparable knowledge, skills and abilities have been attained. Individuals with a bachelor’s degree in psychology, or pursuing a degree in a related field are preferred. Those with experience and interest in neuroscience, clinical psychology, and/or neuroimaging are strongly encouraged to apply. 

Requires strong interpersonal and communication skills. 

The Mind Research Network is division of Lovelace dedicated to advancing the diagnosis and treatment of mental illness and brain injury.

Headquartered in Albuquerque, New Mexico, MRN consists of an interdisciplinary association of scientists located at universities, national laboratories and research centers around the world and is focused on imaging technology and its emergence as an integral element of neuroscience investigation.

With an extended community of academicians, researchers, graduate students and technicians, the MRN is uniquely positioned with its national infrastructure to link the brightest minds in neuroscience with some of the most cutting-edge neuroimaging capabilities in the world today.

The Department of Emergency Medicine at is looking for a full-time Research Coordinator. As a Research Coordinator onsite at one of our primary care clinics, the role will be to coordinate several study tasks related to adolescent substance use prevention and brief intervention activities. The Research Coordinator will report to Drs. Deepa Camenga and Uche Aneni and also work closely with research collaborators at Partnership to End Addiction.

This position is funded by PCORI (Patient-Centered Outcome Research Institute) through September 2028. Duration of employment is limited to the duration of the grant. Those with a background in social science research and/or an interest in applying to graduate school in medical or behavioral sciences are encouraged to apply.

Principal Responsibilities: Recruit and consent adolescents and caregivers in pediatric primary care (PC) waiting areas by pitching a brief introduction to the study. Coordinate research activities with families, pediatricians, and other PC staff. Participate in provider training and fidelity monitoring activities, including on-site practice of study interventions. Communicate with study families, provide technical support as needed, and assist with additional tasks related to consenting participants and collecting data. Track study families to administer follow-up assessments. Attend research training and consultation meetings for PC staff. Participate in multi-site/multi-team meetings virtually and in person. Manage REDCap project database and track online study data. Coordinate collection of research data submitted by study families and pediatricians on hand-held tablets. Assist with cleaning and coordinating study data for data analysis.

The DREAM and REAL-TIME research labs at the University of Central Florida (UCF) are seeking a full-time postdoctoral scholar to lead research projects focused on substance use and the utilization of advanced technology. This position is part of an NIH-funded project testing a mobile application-based intervention for improving alcohol treatment outcomes.

About the Position

The postdoctoral scholar will work closely with Dr. Lidia Meshesha and Dr. Robert Dvorak on clinical research for substance use disorders. The appointment is for 2 years, applications will be reviewed until position is filled. Current research projects concentrate on:

• Testing mobile application-based interventions for substance use disorders
• Increasing rewarding and substance-free activities to improve alcohol treatment outcomes
• Utilizing advanced technology in addiction research and treatment

Responsibilities

The postdoctoral scholar will:

• Contribute to project coordination for NIH-funded research
• Supervise participant recruitment, assessments, and research assistants
• Oversee data management and analysis
• Participate in manuscript preparation and conference presentations
• Engage in grant writing and submissions
• Have opportunities to develop independent research projects
• Participate in teaching and mentoring activities

We are seeking a research coordinator for a NIDA funded study on drug use disorders among underserved groups. This Research Coordinator will be conducting a multi-site data (Jefferson County and Fayette County) collection project focused on drug use disorders. The Research Coordinator in this position will direct all day-to-day operations of a large federally funded, multi-site research project that will need to recruit and interview adults across the lifespan. The Research Coordinator will directly supervise interviewers working in the field. Frequent travel to downtown Louisville (Jefferson County) will be a requirement for this position.

Rutgers, The State University of New Jersey is seeking a Research Project Assistant for the Center of Alcohol & Substance Use Studies.

Among the key duties of the position are the following:

• Participates in several federally funded addiction and trauma research projects.
• Handles subject recruitment, community engagement, and coordination of study visits.
• Assists the principal investigator in preparing regulatory documentation for the institutional review board and funding agencies.
• Trains new research staff and students.
• Provides general administrative support (e.g., ordering supplies, record keeping).
• Handles data management and analysis.
• Performs literature reviews.
• Assists with preparation of grant proposals and research dissemination.

This is an exciting opportunity for someone to contribute to a National Institute for Health Research (NIHR) funded Randomised Controlled Trial in the area of managing drug dependence. The trial is being led by Professor Catriona Matheson at the Centre for Healthcare and Community Research (CHeCR) at the University of Stirling, in close collaboration with The Centre for Healthcare Randomised Trials (CHaRT), University of Aberdeen. This project aims to reduce the use of high-risk street benzodiazepines, which contribute to drug related deaths in people who are also enrolled in Opiate Agonist Treatment (OAT) e.g. methadone. The trial includes at least six sites across Scotland and England with a built-in pilot study, process evaluation and toxicology surveillance study. The research assistant will work closely with the trial’s senior researcher across the needs of the study, with a particular focus on the toxicology study including drug surveillance and scanning and supporting project meetings. They will also contribute to literature reviewing, quantitative data analysis, ongoing communication, report writing and dissemination of outputs. This is a rare opportunity to join an excellent multidisciplinary team from across the UK. Details on the trial team can be found here: https://www.fundingawards.nihr.ac.uk/award/NIHR163461

There may be potential to undertake a PhD study linked to the project. The post holder will be expected to work from the University campus at least two days per week.

Informal enquiries to: Dr Karen Berry karen [dot] berry [at] stir [dot] ac [dot] uk (karen[dot]berry[at]stir[dot]ac[dot]uk)

Description of Duties:

• Undertake surveillance of data sources around new ‘street’ benzodiazepines
• Liaise with external organisations to identify emerging new ‘street’ benzodiazepines that emerge in the UK market over the course of the trial including Public Health Scotland (RADAR), The Specialist Police harm surveillance team, and the European Monitoring Centre for Drugs and Drug Addiction (EMCDDA)
• Review monthly testing results from specialist toxicology lab
• Scanning the academic literature for other relevant research
• Supporting project meetings
• Conducting quantitative analyses
• Participate in writing and disseminating outputs
• Support the Chief Investigator with communications

The University of New Mexico's Project ECHO is looking for a Senior Program Manager to join our ECHO Africa team based in Nairobi, Kenya. This position will play a key role in working with senior Ministry of Health officials, academic partners, the World Health Organization, Africa CDC, and local, regional and international non-governmental organizations in Africa to implement the ECHO virtual, case-based learning approach to support their health priorities. This is a full-time contractual position through the end of 2025 with the possibility of extension.

The objective of the ECHO Africa Senior Program Manager position is to work with senior level officials to design, implement and evaluate the ECHO learning approach as a digital learning tool to build capacity and address critical health priorities. Activities will include engaging in strategic planning, and providing focused training, support and guidance to incountry and regional partners to design and implement relevant ECHO programs. As a key member of the ECHO Africa team, the ECHO Africa Senior Program Manager will be responsible for managing the strategic and operational planning, establishment, execution, and evaluation of ECHO programs in multiple countries in Africa.

In alignment with UNM, Project ECHO, ECHO Africa, and the SILC initiative, the ECHO Africa Senior Program Manager will perform the following duties:

1. ECHO Advocacy

• Participate in the regular review of the ECHO Africa strategic plan in partnership with ECHO Africa Director and staff.
• Engage with senior MOH and other partners to explore how the ECHO virtual learning model can contribute to training and capacity building efforts to address critical health and education priorities.
• Work with partners to develop and implement a strategic plan for ECHO in their country/region.
• Work with team members to support ECHO fundraising efforts.

2. ECHO Coordination

• Provide strategic and technical guidance and training in the design and implementation of ECHO programs with in-country partners.
• Serve as a liaison between in-country partners and the UNM ECHO Institute, iECHO support teams, and other stakeholders.

3. ECHO Operations

• Support ECHO program teams with IT support, site assessments, iECHO on boarding, coordination of sessions, and M&E activities.
• Facilitate and enhance day-to-day working relations with ECHO program teams, partners and other stakeholders, as appropriate to the position.
• Prepare monthly and other reports as required.
• Perform other related duties, as required by the functional supervisor.
• Travel up to 30% or more may be required based on the program work plan and request for support from country partners.

4. ECHO Capacity Building and Technical Assistance

• Support ECHO Partner Launch Trainings for partners as needed.
• Provide ECHO capacity building and operational support as required to in-country ECHO program teams.
• Provide basic technical assistance as needed to ECHO program teams. Advanced technical support will be available from the ECHO Institute and ECHO India.

Montclair State University invites applications for a temporary Associate or Full Professor specializing in Harm Reduction. The successful candidate will hold a concurrent appointment as Director of the Center for Harm Reduction, a research-focused initiative serving as a statewide hub for research, education, and policy development addressing harm reduction strategies and substance use disorders. The Director will have expertise in harm reduction and community-based public health research responsible for shaping the Center’s vision, securing external funding, leading research initiatives, and fostering collaborations with policymakers, community organizations, and other stakeholders.

This temporary, full-time, 12-month faculty position seeks candidates with demonstrated excellence in scholarship, teaching, research, community engagement, and leadership. Primary responsibilities emphasize faculty research and teaching, complemented by administrative leadership of the Center.

Major responsibilities include:

• Teaching one course per semester during the academic year

• Develop and implement the Center’s strategic plan in alignment with the University’s mission.  

• Establish partnerships with academic institutions, government agencies, and community-based organizations to advance harm reduction efforts.  

• Lead and oversee interdisciplinary research projects focused on harm reduction, substance use disorder treatment, and related public health issues.  

• Securing and managing external funding from state, federal, and private sources to support and expand research initiatives.

• Collaborating with policymakers, academic institutions, and community organizations to translate research into actionable policy recommendations.

• Developing and disseminating policy briefs, evaluation frameworks, and evidence-based recommendations to state and federal stakeholders.

• Overseeing and managing the Center’s strategic vision, daily operations, budget, staffing, and compliance with university and grant requirements.

• Supervising and mentoring research staff, faculty affiliates, and program coordinators.

• Enhancing existing university harm reduction initiatives, including the Harm Reduction Certificate program and workforce training modules.

• Perform other duties as assigned.

• Management retains the right to add or change job duties at any time.

The Department of Psychology at the University of Houston (UH) seeks to hire a Research Assistant Professor for the Research on Emotions, Treatment Outcomes, and Health Equity (RESTORE) Lab to conduct research on funded grant projects. UH is a Carnegie-Designated Tier One Public Research University. The successful applicant will be asked to conduct research transdiagnostic processes in the context of addiction, mental and physical health conditions. Applicants should have a Ph.D. in Clinical Psychology, or equivalent, and an established track record in publishing peer reviewed articles on transdiagnostic processes with an emphasis on mental health (e.g., anxiety, depression, transdiagnostic factors) and physical health disorders (e.g., chronic pain) and contributions to grant activities. Experience in developing a line of research is preferred. Record of previous grant funding is also preferred. This position is for one year, beginning July 1, 2025 (anticipated), with the possibility of renewal.

All positions at the University of Houston-System are security sensitive and will require a criminal history check.

The University of Houston System and its universities are an Equal Opportunity Institution.

Description:

Assists the principal investigator with artificial intelligence/machine learning research.

1. Designs solutions and sets up experiments in hybrid research environment.
2. Researches artificial intelligence/machine learning algorithms, database design, deep learning, big data, and cloud computing.
3. Publishes research in peer review journals; presents research at conferences.
4. Writes technical reports and other project-related documents.
5. Performs other job-related duties as assigned.

MQ: Doctorate degree in computer science, electrical or computer engineering, or related field; and (3) years related experience

The primary purpose of this position is to undertake research on a 3-year NHMRC Ideas grant titled “Reducing alcohol consumption through the sober curious movement”. The Research Fellow will work with a research team from Torrens University Australia (Prof Paul Ward is leading the study), La Trobe University, Monash University, the University of Auckland and Columbia University New York, including Chief Investigators, other funded researchers and PhD students.  This is a 3-stage mixed-methods study: Stage 1 will include a social media analysis of alcohol-free marketing and interviews with producers; Stage 2 will include interviews with high alcohol consuming groups; Stage 3 will co-develop interventions for alcohol reduction. The study aims to understand the social worlds of drinking and the potential for sober curiosity in four 4 heavy drinking ‘case-study’ groups: 1) male construction workers, 2) hospitality sector workers, 3) LGBTQ+ women and 4) tertiary education students (university and TAFE) living in regional areas. This Research Fellow position at Torrens University will primarily be responsible for all stages of the study for ‘male construction workers’ and ‘LGBTQ+ women’ but will also be required to contribute to the other two case-study groups when required.

Day-to-day accountabilities: 

• Implement a research plan in line with the funded NHMRC research proposal (available on request) 

• Achieve required research outputs in line with the research budget available and as set for you by your manager and outlined in the research plan 

• Undertake data collection and analysis and prepare reports, presentations, communications, grant submissions and other correspondence  

• Manage appropriate administration related to research work  

• Deliver and coordinate research seminars related to individual research outputs as required  

• Maintain strong collaborative working partnership with all key working relationships

This is a 3-year Fixed term position. The primary Chief Investigator is in Adelaide, which would be the preferred location, but you could also be in Melbourne, Sydney or Brisbane (where Torrens University has campuses).

The primary purpose of this position is to undertake research on a 3-year ARC Discovery grant titled “From Oppression to Hope: Reducing Heavy-Drinking with Midlife Women”. The Research Fellow will work with a research team from Torrens University Australia (Prof Paul Ward is leading the study), La Trobe University, and the University of Adelaide, in addition to collaborators in universities in New Zealand, England, the US and Canada. The research fellow will be part of a research team which includes Chief Investigators, Partner Investigators, other funded researchers and PhD students.  The study will work out ways to support the following groups of midlife women to reduce their alcohol consumption (and their breast cancer risk): 1) women living in regional areas of Australia; 2) LGBTQ+ women; 3) women living in poverty; and 4) women working in the corporate sector. This is a 3-stage study: Stage 1 will include an ethnography, netnography, photo elicitation, social media analysis and qualitative interviews; Stage 2 will include deliberative dialogue groups to identify ‘systems level’ drivers of alcohol consumption; Stage 3 will co-develop and implement interventions aimed at increasing critical consciousness and hope for the case-study groups. This Research Fellow position at Torrens University will primarily be responsible for all stages of the study for ‘LGBTQ+ women’ and ‘women in the corporate sector’ but will also be required to contribute to the other two case-study groups when required.

Day-to-day accountabilities: 

• Implement a research plan in line with the funded ARC research proposal (available on request) 

• Achieve required research outputs in line with the research budget available and as set for you by your manager and outlined in the research plan 

• Undertake data collection and analysis and prepare reports, presentations, communications, grant submissions and other correspondence  

• Deliver and coordinate research seminars related to individual research outputs as required  

• Maintain strong collaborative working partnership with all key working relationships 

• Manage administration related to research work including but not limited to process invoices, payments and expenses related to research

​This is a 3-year Fixed term position. The location can be Sydney, Melbourne, Brisbane, Adelaide.

The Clinical and Social Research Team at Turning Point is seeking a Clinical Research Associate to support key addiction treatment trials, including major NHMRC and MRFF funded studies like MPATHY, which explores MDMA-assisted therapy for PTSD and Alcohol Use Disorder. This is a vital role in coordinating and delivering high-impact research within a growing program focused on advancing evidence-based addiction care.

The Clinical Research Associate will support key trial activities including site setup, staff training, data monitoring and regulatory submissions. The role is central to maintaining ethical compliance, audit readiness and smooth coordination across multiple sites through clear documentation and effective stakeholder engagement.

We are seeking someone with strong experience in clinical trial coordination, supported by relevant qualifications or equivalent training. Success in this role will require excellent project management skills, stakeholder engagement and a solid understanding of ethical and regulatory requirements.

If you are motivated by contributing to high-quality addiction research that has real-world impact, we encourage you to apply.

Monash University seeks applicants for this opportunity who are able to demonstrate present valid and current Australian work rights.

About Monash University

At Monash, work feels different. There’s a sense of belonging, from contributing to something ground-breaking – a place where great things happen.

We value difference and diversity, and welcome and celebrate everyone's contributions, lived experience and expertise. That’s why we champion an inclusive and respectful workplace culture where everyone is supported to succeed.

An exciting opportunity has arisen for a dynamic and innovative individual to join the Cwm Taf Morgannwg Local Public Health Team working as a Principal Public Health Practitioner.

This is a strategic role focusing on substance use, jointly funded by the Cwm Taf Morgannwg Area Planning Board (APB) and Cwm Taf Morgannwg University Health Board (CTMUHB) and hosted by the CTMUHB Public Health Team.

The role will work closely with the officers of the APB, and as a senior member of the CTMUHB Public Health Team. Alcohol and drugs are lead contributors to morbidity and mortality within our region, and there is an urgent need to build our strategic approach.

The post holder will be a member of the strategic group of the CTMUHB Public Health Team and provide public health expertise to the work of the APB, working in close partnership with the APB officers, who are hosted by Rhondda Cynon Taf County Borough Council.

We are committed to agile working and will involve home working alongside working in office sites across Cwm Taf Morgannwg, including co-locating with APB officers in Rhondda Cynon Taff.

Main duties of the job

The role will be responsible for:

• Raising the profile of the substance use agenda regionally and within CTMUHB.
• Providing local leadership and strengthening our strategic approach to reducing the harms from alcohol and drugs.
• Providing public health expertise to the commissioning cycle for substance use services in CTM.
• Connecting across the developing regional health protection system and harm reduction agenda.

There will be opportunities to work alongside colleagues at a national level as we advocate for stronger leadership and action on substance use in Wales. As a new post, there is an opportunity to develop the role as priorities emerge in collaboration with the APB and Public Health Consultant.

It will be essential to work with a range of partner agencies and within CTMUHB against the priorities of the APB, health board and national strategy as it develops. Experience of working in substance use or commissioning will be valued.

About us

Cwm Taf Morgannwg University Health Board is part of the NHS Wales family. Our Health Board provides primary, secondary and community health and wellbeing services to around 450,000 people living in three County Boroughs: Bridgend Merthyr Tydfil, and Rhondda Cynon Taf.

We live by our core values:

• We listen, learn and improve
• We treat everyone with respect
• We all work together as one tea

We are a proud local employer; around 80% of our 15000 workforce live within our region, making our staff not only our lifeblood of our organisation but of the diverse communities that we serve.

Background

This post will be funded by a multi-million pound award from Wellcome Leap programme awarded to the University of Birmingham to study Untangling Addiction. Our project, entitled “Predicting persistent opioid usage after surgery: Integrating multi-omics, neurobiology, and AI-interviews".

Our research programme aims to address persistent opioid usage by identifying molecular, neurobiological and cognitive signatures characterizing patients at risk of prolonged opioid use post-surgery.

Role Summary

This post-doctoral research will be conducted in collaboration with a multidisciplinary team of experts in the fields of neuroscience, immunology, pain, anaesthesia, and machine learning. 

Supervision will be provided by Prof. Ali Mazaheri, as well as Prof. Fang Gao Smith, and Prof. Helen McGettrick.

The successful candidate will have a strong background in psychology, cognitive science and multi-modal data integration. Experience, in particular in combining different modalities (longitudinal data, multi-omics, EEGs, NLP, etc.), is a clear advantage. 

In your online application please include detail on how you match the person specification.

Main Duties

The responsibilities may include some but not all of the responsibilities outlined below.

• Developing novel computer-based models, techniques and methods 
• Develop research objectives and proposals for own or joint research, with assistance of a mentor if required
• Contribute to writing bids for research funding
• Analyse and interpret data
• Apply knowledge in a way which develops new intellectual understanding
• Disseminate research findings for publication, research seminars etc
• Supervise students on research related work and provide guidance to PhD students where appropriate to the discipline
• Contribute to developing new models, techniques and methods
• Undertake management/administration arising from research
• Contribute to Departmental/School research-related activities and research-related administration
• Contribute to enterprise, business development and/or public engagement activities of manifest benefit to the College and the University, often under supervision of a project leader
• Collect research data; this may be through a variety of research methods, such as scientific experimentation, literature reviews, and research interviews 
• Present research outputs, including drafting academic publications or parts thereof, for example at seminars and as posters 
• Provide guidance, as required, to support staff and any students who may be assisting with the research 
• Deal with problems that may affect the achievement of research objectives and deadlines
• Promotes equality and values diversity acting as a role model and fostering an inclusive working culture.

We are seeking two full time research assistants on fixed-term contracts until 31/10/2029 with the NIHR Mental Health Research Groups-funded Centre for Addiction and Mental Health Research at the University of Hull. The successful candidates will become part of a larger interdisciplinary team of researchers investigating addiction and mental health conditions. Under the leadership of Professor Thomas Phillips, Professor of Nursing in Addiction and Professor Judith Cohen, Hull Health Trials Unit, the research team has secured a five-year award, supported by our partners at the University of York and King’s College London, to develop addiction and mental health research based at the University of Hull. The research targets national priorities and the mental health needs of our population with the aim of improving access to care and treatment that works. Working closely with health and social care providers as well as patients and the public, we have developed an ambitious programme of research across three themes:

Theme 1: Improving care pathways and outcomes for young people with substance use and mental health problems

Theme 2: Improving care pathways for adults with substance use disorder and mental health problems presenting to places of safety and emergency departments

Theme 3: Defining the needs of adults with alcohol-related cognitive impairment 

The posts will provide flexible support across the themes, with an initial focus on themes 2 and 3. The roles will be varied and will include supporting systematic and scoping reviews, assisting with the development of research protocols and study documents and seeking regulatory approvals, and supporting the delivery of research projects through the recruitment of participants and collection of data.

We are seeking exceptional graduates with experience of literature reviews, data collection and analysis and drafting research reports. The successful candidates will join a thriving community of researchers examining the impact of addiction and mental health problems on health, social care and criminal justice settings. The research assistants will support the research fellows, co-investigators and patient and public contributors to collate the evidence base and assist in the development and delivery of research projects.

The posts will be based in the award winning Allam Medical Building, University of Hull. The Centre for Addiction and Mental Health Research is part of the thriving academic community within the Faculty of Health Sciences including postgraduates studying PhDs. The research team provides outstanding methodological expertise in high-quality clinical and applied health research.

The ideal candidates will have excellent verbal and written communication skills, knowledge and skills in relation to conducting literature reviews, experience in delivering clinical research, and experience engaging with vulnerable people in clinical or research settings.  

An exciting opportunity has arisen to join an enthusiastic and dynamic team in Islington. 

This post is for 1.0 WTE Consultant Psychiatrist working within the Islington Better Lives Drug and Alcohol Service and has arisen from current postholders reducing their sessions and additional investment in the service from OHID.

The post is available from 1st October 2025 and is being offered as a substantive post pending approval by The Royal College of Psychiatrists.

The post-holder will be part of the multidisciplinary team which includes both statutory and voluntary sector roles and provides holistic care to patients. The service is primarily community based and is delivered from 3 community sites. The post holder will work across these sites with 1.3 other substantive Consultant Psychiatrists, locally employed GPs, core trainee and specialty doctor.

National terms and conditions apply to this post. Inner London Weighting applies.

Main duties of the job

This is a full time Substantive position for 10 Programmed Activities: 7.5 Direct Clinical Care and 2.5 Supporting Professional Activities.
The medical team is currently led by two part time Consultant Psychiatrists, who both cover the borough across all three sites. There is a part time GP with a special interest in substance misuse based at SSR one day a week. There is a core psychiatry trainee based predominately at SSR across the week with some offsite training commitments. There is another core trainee based at GIR who does a split post with the Islington Psychotherapy service and other off site training commitments.
The post holder will work with the medical team to ensure rapid access to treatment and can expect to offer 2-3 assessments/follow ups per clinic depending on demand. There is plenty of opportunity for service development in this dynamic, innovative service.
The primary record-keeping system for the service is RiO, general electronic patient record system of the Trust. Read only access to EMIS is available to senior clinicians to aid communication and integration with other primary care services.  

The post-holder will be provided with appropriate technology (laptop, mobile) in order to facilitate agile working across multiple sites. The team has office space at the Margarete Centre with dedicated admin support.

An exciting opportunity has arisen within the Housing Inclusion Service for a committed, enthusiastic individual who wants to make a real difference to the lives of some of our most vulnerable residents who are experiencing complex needs and are rough sleeping in the borough.

Reporting to the Rough Sleeping Coordinator, the successful applicant will work with a targeted group of clients who have no recourse to public funds, and who also have alcohol or substance misuse dependency, often alongside other complex needs. As a Housing Engagement worker, you will support these clients to access immigration advice, specialist treatment agencies and health providers, as well relevant Housing services.

You will work collaboratively with internal and external stakeholders to provide a holistic, targeted and effective programme of support which focuses on enabling people to secure and sustain settled accommodation.

For an informal discussion about this opportunity, please contactCharlie Uddin; Charlie [dot] Uddin [at] royalgreenwich [dot] gov [dot] uk (Charlie[dot]Uddin[at]royalgreenwich[dot]gov[dot]uk) .

The Center for Dissemination and Implementation Science (CDIS) led by Dr. Sara Becker is within the Institute for Public Health and Medicine (IPHAM) at the Feinberg School of Medicine. The central vision of CDIS is to bridge the gap between public health/medical knowledge (what we know) and public health/medical practice (what we do). D&I science is essential to realize the full impact of public health and medical research. Traditional, passive dissemination strategies such as publishing clinical recommendations, trials, or guidelines are insufficient for realizing practice change. Innovative, proactive strategies for increasing the implementation and sustainability of evidence-based interventions in community and clinical settings are essential for improving population health and driving health care innovation.

This Research Study Assistant (RSA) will support the Principal Investigator on an NIH-funded implementation initiative focused on promoting the uptake of contingency management (CM) within community-based organizations across Chicagoland. The research program involves implementation of CM, an intervention in which patients earn incentives for meeting treatment goals, and it is carried out in partnership with the Chicago Department of Public Health (CDPH). Activities include communicating with CDPH and partnering community-based organizations via phone/Zoom/email; assisting with CM trainings for organization staff; outreach to research participants for completion of study assessments at multiple timepoints following study protocols; and listening to role plays of treatment delivery to provide feedback on fidelity. The RSA is also expected to help with the organization and maintenance of project documents and files and assisting the Research Project Coordinator with the continual submission of IRB documents, annual grant progress reports, and data safety monitoring board reports. 

This RSA may have the opportunity to assist on other NIH-funded research programs, including (1)

a support center that helps projects funded through the National Institute on Drug Abuse to infuse implementation science methods, models, and measures into their work (RASC) and (2) a large pragmatic effectiveness randomized controlled trial evaluating whether a technology-assisted intervention can improve the outcomes of adolescents in residential treatment (Parent SMART). 

The RSA will complete all activities by strictly following Good Clinical Practices (GCP) & all relevant current local, state, & federal laws, regulations, guidance, policy & procedure developed by the NU Institutional Review Board (IRB), Food & Drug Administration (FDA) Code of Federal Regulations (CFR), & the International Conference on Harmonization (ICH).

Specific Responsibilities:

Technical

• Recruits study participants. 
• Reviews & obtains informed consent. 
• Schedules study visits with participants. 
• Conducts interviews. 
• Scores test results. 
• Collects survey data. 
• Facilitates communication with key personnel & participants to maintain project study flow. 

Administration

• Participate in, organize, and develop materials (e.g., agendas, minutes, summaries) for internal and external meetings and site-visits in collaboration with study team. 
• Maintains detailed records of results which may include collecting, extracting & entering data; &/or preparing basic charts & graphs. 
• Performs scientific literature searches in support of research. 

Finance

• Submit for reimbursements for participants.

Supervision

• May train other research staff to interview/test participants.

Miscellaneous

• Performs other duties as assigned.

This specific Research Assistant II (RA2) position will support the Vice Chair for Addiction Psychiatry, Dr. Amy Yule, on research projects within the Department of Psychiatry. The main project the RA2 will be involved with is a community-based clinical program targeted towards adolescents and young adults with frequent substance use and psychosis symptoms. The Research Assistant II duties will include, tracking patient participation in the program, administering baseline and follow-up questionnaires, entering and updating data, maintaining databases, running reports, providing meeting support, and performing other administrative tasks.

Position: Research Assistant II, Psychiatry Research

Location: Boston, MA       

Schedule: 40 hours per week, On-site

ABOUT BMC:

At Boston Medical Center (BMC), our diverse staff works together for one goal — to provide exceptional and equitable care to improve the health of the people of Boston. Our bold vision to transform health care is powered by our respect for our patients and our commitment to ensure everyone who comes through our doors has a positive experience.

You’ll find a supportive work environment at BMC, with rich opportunities throughout your career for training, development, and growth and where you’ll have the tools you need to take charge of your own practice environment.  

POSITION SUMMARY:

The RA2 will oversee the administrative aspects of the grant and interact with study subjects, clinical research coordinators, study investigators, work study students and other research staff.  Duties include assisting with patient recruitment, scheduling study visits, administering questionnaires, creating and filing case report forms, entering and updating data, maintaining databases, running reports, storing samples, and performing other administrative tasks. The RA2 maintains contact with the participating sites to insure complete and timely data collection, maintains patient profiles, assists with documenting financial and budgetary needs of the grant, and supports the research team with the preparation of data and reports.  Oversees work of Research Assistants, along with training and orientation. 

JOB RESPONSIBILITIES:

• Provides assistance in the development of reports, presentations, and data analysis. Assists in data collection and provides feedback on study’s progress.
• Recruits subjects to participate in the study by using approved methodologies. Makes independent judgements of suitability of potential participants for clinical trials. Develops and implements patent recruitment strategies.
• 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.
• Reviews the data collection forms for each enrollee for completion and quality; checks work of junior staff performing data entry to ensure timely and accurate entry.  Recommends changes to protocols and evaluates data.
• Assists Investigators with manuscript and presentation preparation and research. Conducts literature searches.
• Oversees work of research assistants. Provides technical guidance to junior staff.