AVAILABLE POSITIONS

HIV/AIDS Clinical Consultant

SUMMARY

GSSHealth is seeking an HIV/AIDS Clinical consultant to provide strategic direction and technical support for an HIV clinical care strengthening program in 6 countries in sub-Saharan Africa. This consultancy will be based in Baltimore and is contingent upon available funding. If the program is funded, expected start date is September 2021.

 

ESSENTIAL FUNCTIONS

  • Provide strategic direction for program planning to support clinicians who offer HIV/AIDS services in 6 countries

  • Offer technical support on best practices for HIV prevention, care and treatment, in alignment with current international guidance and

  • Provide direction on the implementation of sound HIV prevention, care and treatment processes

  • Troubleshoot barriers and help provide solutions to programmatic barriers

  • Build positive relationships within the team and with external parties

  • Participate in teleconferences and communicate with local stakeholders

  • Evaluate available data and make process improvements or corrections as needed

QUALIFICATIONS

  • Medical degree with experience in HIV OR MPH or Master’s degree in related field with demonstrated experience of 5+ years in HIV/AIDS clinical programs.

  • Excellent verbal and written communications skills.

  • Proficiency in French is desirable.

  • Ability to guide and facilitate stakeholder collaboration

  • Ability to work with diverse teams; experience in resource-limited settings is desirable.

HIV Program Coordinator

SUMMARY

GSSHealth is seeking a full-time Program Coordinator to manage an HIV care strengthening program in 6 countries in sub-Saharan Africa. This position will be based in Baltimore and is contingent upon available funding. If the program is funded, expected start date would be around September 2021.

ESSENTIAL FUNCTIONS

  • Facilitate the planning, initiation and execution of a new HIV program

  • Ensure the implementation of policies and program deliverables

  • Build positive relationships within the team and with external parties

  • Schedule and lead teleconferences, take minutes and follow-up on action items

  • Keep updated activity records and create reports as needed

  • Evaluate available data and make process improvements or corrections as needed

QUALIFICATIONS

  • Bachelor’s degree in public health or a related subject and 2-3 years of related experience, OR Master’s degree in public health or a related field.

  • Excellent verbal and written communications skills.

  • Fluency in French  

  • Ability to guide and facilitate stakeholder collaboration

  • Ability to work independently with minimal supervision.

  • Ability to work with diverse teams; experience in resource-limited settings is desirable.

  • Proficiency with Microsoft Office programs.

  • Attention to detail and ability to grasp technical concepts.

Clinical Research Associate

SUMMARY

GSSHealth will be seeking a full-time Clinical Research Coordinator / Senior Clinical Research Coordinator in the coming months to establish, coordinate and monitor research studies at sites in / across multiple countries. This position will be based in Baltimore and is contingent upon available funding.

ESSENTIAL FUNCTIONS

  • Provide input on study protocols

  • Manage study protocol compliance

  • Maintain appropriate study files and records

  • Participate in study teleconferences with sponsor and study staff; follow-up on communications

  • Support site feasibility assessments and site checklists

  • Compile information for reporting purposes

  • Develop and harmonize study plans and SOPs across study sites for compliance with study protocol

  • Co-develop standard study SOPs for testing, sample collection, storage, shipment for different sample types

  • Support development of QA/QC processes for lab testing required for the study, conduct QC checks

  • Support and organize study trainings

  • Assist with specifications for procurement of study laboratory reagents and supplies

QUALIFICATIONS

  • Bachelor’s degree in life science of health-related discipline and 2-3 years of experience in clinical research monitoring OR Master’s degree in related field.

  • Previous job experience as a CRA

  • Demonstrated knowledge of GCLP, ICH, Human Subject Protection.

  • Excellent verbal and written communications skills.

  • Ability to work independently with minimal supervision.

  • Ability to work with diverse teams; experience in resource-limited settings is desirable.

  • Proficiency with Microsoft Office programs.

  • Attention to detail and ability to grasp technical concepts.

As an equal opportunity employer, we do not discriminate on the basis of race, color, religion, national origin, gender, gender expression, pregnancy, age, disability, marital status, sexual orientation, or genetic information, in any of our activities or operations.

Applicants must be authorized to work in the US.

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