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Axle Informatics is a bioscience and information technology company that offers advancements in translational research, biomedical informatics, and data science applications to research centers and healthcare organizations around the globe. With experts in biomedical science, software engineering, and program management, we focus on developing and applying research tools and techniques to empower decision-making and accelerate research discoveries. We work with some of the top research organizations and facilities in the country including multiple institutes at the National Institutes of Health (NIH).
Benefits: 100% Medical, Dental & Vision Coverage for Employees Paid Time Off (Including Holidays) Employee Referral Bonus 401K Match Tuition reimbursement and professional development opportunities Flexible Spending Accounts:
Healthcare (FSA) Parking Reimbursement Account (PRK) Dependent Care Assistant Program (DCAP) Transportation Reimbursement Account (TRN) Overview Axle is looking to add a driven, flexible, organized, and meticulous Clinical Protocol Coordinator to our dynamic team. The Contractor(s) shall provide services in support of the overall functions of the Office of the Director (OD), Division of Clinical Research (DCR). Technical Requirements: Assist with facilitation of the PREVAC retention study implementation, analysis, and manuscript writing process with the key objective of building capacity, developing infrastructure and providing support to advance the study through its completion
Work closely with the PREVAC retention study principal investigators, site PIs and study teams to improve protocol implementation to achieve the study objectives
Assist with and participate in conducting regular meetings with site managers, PIs, study teams, and others to review and advance progress of the PREVAC retention study
When appropriate, involve the appropriate governance committees to provide direction to study teams to resolve issues, obstacles to enhance the achievement of study goals
Assist with prioritization of needs and provide solutions to overcome gaps or obstacles to study completion
Assist with facilitation of sharing of best practices across the multiple teams and sites participating in the study, creating efficiencies and leveraging processes improvements
Support and assist PREVAC study site medical and community engagement teams in all aspects of the PREVAC retention study analysis and data interpretation
Assist in understanding and delineating how the engagement between the site medical/scientific staff, and the community engagement/social mobilization staff, with study participants, took place, particularly the approaches and methods utilized for participant retention
Assist with review of participant interview and site staff focus group transcriptions and translations to help assure quality and cultural contextual fidelity
Assist with organization of qualitative analysis training and participate in training of site staff as required to advance and complete the retention study
Support and assist with coding of participant interview and focus group discussion transcripts, by in-country investigators, in collaborative qualitative analysis
Assist with teaching the Atlas.ti system for qualitative analysis coding, and serve as a back-up coder, as needed, for qualitative interview and focus group data, to assure the timely and full completion of study data preparation and coding
Assist in coordinating the use of the Atlas.ti-generated retention study database, by site PIs and colleagues, and assuring that investigators have the skills and capacity to complete the analysis
Support and facilitate writing and review of material for reports, publications in peer-review journals, and presentations by site PIs and staff as part of both study-wide and country-specific analyses and outputs
Specific Qualifications: Bachelor's degree in a related field is required.
Demonstrate adequate education, training and experience to conduct the clinical investigation.
Able to communicate effectively with all levels of clinical staff, render recommendations and policy interpretation, independently identify problems and effectively offer solutions.
Experience in clinical research setting with protocols and clinical trials.
Excellent writing skills in English and French.
The diversity of Axle's employees is a tremendous asset. We are firmly committed to providing equal opportunity in all aspects of employment and will not tolerate any illegal discrimination or harassment-based age, race, gender, religion, national origin, disability, marital status, covered veteran status, sexual orientation, status with respect to public assistance, and other characteristics protected under state, federal, or local law and to deter those who aid, abet, or induce discrimination or coerce others to discriminate.
Accessibility: If you need an accommodation as part of the employment process please contact: ******** Disclaimer: The above description is meant to illustrate the general nature of work and level of effort being performed by individual's assigned to this position or job description. This is not restricted as a complete list of all skills, responsibilities, duties, and/or assignments required. Individuals may be required to perform duties outside of their position, job description or responsibilities as needed.
This role has a market-competitive salary with an anticipated base compensation range listed below. Actual salaries will vary depending on a candidate's experience, qualifications, skills, and location.
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Salary Range
$75,000—$80,000 USD