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  • ID
    #50624173
  • Job type
    Full-time
  • Salary
    $27.88 USD per hour
  • Source
    California
  • Date
    2023-12-01
  • Deadline
    2024-01-30

Research Associate

California, San francisco bay area 00000 San francisco bay area USA
 
Full-time

Vacancy expired!

Description

Heluna Health invites applications for the full-time position of Research Associate in the Center on Substance Use and Health (CSUH) at the San Francisco Department of Public Health.

CSUH conducts pharmacologic and behavioral interventions, observational studies, and related activities to maximize the health outcomes of people who use alcohol, methamphetamine, opioids, cocaine, and other substances. We work with people who are actively using substances, and focus on meeting their goals related to their substance use, including reduction in use or harms, prevention or treatment of infectious diseases, or prevention of drug overdose. We conduct research in a community-based environment in downtown San Francisco, with the facilities and resources needed to perform complex clinical research studies. We are proud to treat people who use substances with respect and dignity and enjoy a close-knit culture of intellectual curiosity, collaboration, and fun.

Under the supervision of the Program Manager, the Research Associate will be responsible for a wide variety of duties and projects related to behavioral and pharmacologic studies in the fields of HIV prevention and substance use.

This is a temporary, grant-funded, full-time, benefitted position. Employment is provided by Heluna Health. This position has non-standard work hours (may require work during evening hours).

Pay range: $27.88-$30.05

If hired for this position, you will be required to provide proof that you are fully vaccinated for COVID-19 prior to your start date, or have a valid religious or medical reason qualifying you for an exemption (that may or may not require accommodation).

ESSENTIAL FUNCTIONS

Support the investigators of this close-knit research team in the conduct of research protocols within the guidelines of Good Clinical Practice.

Responsible for screening potential participants over the phone or in-office, obtaining informed consent, and proactively managing participant scheduling and conducting study visits.

Perform rapid STI/HIV tests and STI/HIV risk reduction counseling.

Conduct substance use and medication adherence counseling using principles of harm reduction.

Conduct retention efforts for participants over the course of study follow-up schedule.

Other duties include collecting, processing, and testing of blood and urine samples, accurately completing case report forms, setting participants up with computer-assisted questionnaires, and administering assessments.

Perform quality assurance checks of study documents, enter study data into databases such as REDCap, Access, Advantage eClinical, or Excel, and other administrative tasks related to studies.

Assist with other unit studies as needed, including: conducting in-depth interviews and surveys.

Support the development of study operations protocols (SOPS) in close collaboration with the Program Manager.

Other duties as assigned, including coverage for other staff and discrete projects related to ongoing studies within CSUH.

JOB QUALIFICATIONS

Minimum Qualifications

BA/BS in related field, or a combination of relevant experience and education

Knowledge of and sensitivity to diverse communities, particularly communities of substance using persons, people of color, and LGBTQIA+ individuals

High level of attention to detail and ability to handle a variety of tasks with a high degree of accuracy

Excellent writing and interpersonal communication skills

Familiarity with Microsoft Office

Desired Qualifications

Advanced degree in health/mental health or related field

Certified phlebotomist

Certified HIV test counselor

Counseling experience with substance users and/or counseling experience in reducing the risk of HIV acquisition or transmission

Interest and ability to learn a wide array of techniques and technologies and to cross-train to support the duties of other staff members

Experience with clinical trials research and/or healthcare settings

Experience working with challenging participants, or participants with multiple diagnoses

Knowledge of regulations, policies and procedures related to the protection of human subjects and confidentiality

Any other knowledge and skills useful to this research group is considered a plus (software skills, presentation experience, database knowledge, basic website maintenance, etc.)

PHYSICAL DEMANDS

Stand Frequently

Walk Frequently

Sit Frequently

Handling / Fingering Occasionally

Reach Outward Occasionally Reach Above Shoulder Occasionally Climb, Crawl, Kneel, Bend Occasionally

Lift / Carry Occasionally - Up to 50 lbs

Push/Pull Occasionally - Up to 50 lbs

See Constantly

Taste/ Smell Not Applicable

Not Applicable Not required for essential functions

Occasionally (0 - 2 hrs/day)

Frequently (2 - 5 hrs/day)

Constantly (5+ hrs/day)

WORK ENVIRONMENT

General Office Setting, Indoors Temperature Controlled

Heluna Health is an Affirmative Action, Equal Opportunity Employer that encourages minorities, women, veterans, and disabled to apply.

All qualified applicants will be considered for this position in accordance with the San Francisco Fair Chance Ordinance

EEOC STATEMENT

It is the policy of Heluna Health to provide equal employment opportunities without regard to race, color, religion, sex, national origin, age, disability, marital status, veteran status, sexual orientation, genetic information or any other protected characteristic under applicable law.

Please include your resume and cover letter with the application.

Apply here: https://recruiting2.ultipro.com/PUB1001PUBH/JobBoard/6705aa07-0bcb-4660-ad1b-2fda952becc7/OpportunityDetail?opportunityId=91f0e3ca-850c-4587-8597-9cf4b7f493ad

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