Regulatory Affairs Associate

Heluna Health invites applications for the full-time position of Regulatory Affairs Associate. Bridge HIV is a grant-funded research unit affiliated with the San Francisco Department of Public Health and the University of California San Francisco. Under the direction of Susan Buchbinder MD Bridge HIV has been conducting HIV and STI preventive vaccine studies HIV pre-exposure prophylaxis (PrEP) studies (including oral and injectable medications) and other studies of biomedical HIV prevention strategies since the early days of the epidemic. The Bridge HIV Investigators are global leaders in HIV vaccine and prevention science epidemiology of HIV infection HIV medication adherence combination HIV prevention strategies and HIV research training methods. For more information please see .

Under the direct supervision of the Medical Director the Regulatory Affairs Associate will be part of a dynamic team conducting biomedical intervention studies (HIV vaccines pre-exposure prophylaxis and STI prevention).

This is a temporary grant-funded full-time benefitted position. Employment is provided by Heluna Health. This position is onsite Monday-Friday.

Interested individuals should submit a cover letter and resume for consideration.

ESSENTIAL FUNCTIONS
Submit and track Institutional Review Board (IRB) applications for initial review modification renewal and protocol deviations for study protocols
Maintain all study administration documentation (IRB communications sponsor communications licensure study initiation agreements) on-site storage archiving and destruction
Draft Standard Operating Procedures (SOP) and ensure document version control and dissemination for all SOPs consents protocols and amendments
Communicate and collaborate with key study personnel on upcoming projects protocols and operational implementation
Provide guidance to site staff on current research guidelines regulatory and institutional policies
Serve as liaison among study sites DPH and other regulatory entities.
Quality Management System planning and implementation - includes conducting quarterly audits preparing quarterly and annual reports and creating corrective and preventative action plans
Lead and manage the Regulatory Working Group a cross-team collaborative group which meets monthly to revise and develop site SOPs address organization-wide regulatory issues and establish standard practices for reporting and documentation.
Track and ensure staff compliance with mandatory institutional and regulatory training requirements - Includes HSP GCP GLP and SOPs.
Draft review submit and track Corrective and Preventative Action (CAPAs) plans for study protocol deviations in collaboration with study coordinators.

JOB QUALIFICATIONS

Education/Experience
Demonstrates strong commitment to anti-racism and health equity
Degree in biological or social sciences survey research public health law demography or a related field or combination of relevant experience and education
Experience coordinating monitoring or auditing clinical trials
Experience with developing IRB and/or grant applications
Experience creating and implementing quality assurance measures related to clinical and behavioral research

Other Skills Knowledge and Abilities
Detail and deadline oriented. Ability to manage multiple assignments under tight deadlines. Proven skills in setting priorities coupled with demonstrated ability to be flexible
Ability to work independently to use discretion and judgment to make informed decisions and carry out action plans
Ability to implement policies and procedures regarding confidentiality and security
Ability to develop training materials and conduct training workshops or in-services
Ability to use Word Excel PowerPoint Access and project management tools such as Trello
Ability to interpret and follow policy and maintain a high level of confidentiality in performance of duties
Ability to gather synthesize and evaluate information and convey ideas clearly about policies procedures facts and records pertinent to routine and unusual situations
Strong interpersonal skills to establish and maintain cooperative and productive working relationships
Skill in reading and writing and editing standard English text directives business correspondence presentations and technical documents
Knowledge of federal and state laws regulations policies and procedures related to the protection of human subjects
Knowledge of confidentiality issues state and federal laws regulations and policies governing health data privacy including HIPAA
Knowledge of and sensitivity to diverse communities particularly communities of color and gay/ lesbian/ bisexual/ transgender communities

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 to all employees and applicants without regard to age (40 and over) national origin or ancestry race color religion sex gender sexual orientation pregnancy or perceived pregnancy reproductive health decision making physical or mental disability medical condition (including cancer or a record or history of cancer) AIDS or HIV genetic information or characteristics veteran status or military service.

Required Experience:

IC