Outcomes Coordinator Jobs

Excellent organizational and time-management skills; proven ability to independently plan, organize, and implement team-based projects with minimal oversight.

Familiarity with the research pipeline and the process of conducting research. Experience with claims data or clinical/medical knowledge a plus.

Deep understanding and experience with propensity-score matching, inferential and causal statistics, and study design.

Advanced, applied knowledge in programming in SAS and SQL required.

Experience with MS Office tools, especially with PowerPoint.

Experience with reporting, analysis, and data visualization tools (e.g., Python, R, STATA, Tableau, etc.)

Exceptional time management, communication, and organizational skills.

Post-graduate qualification in a related field (e.g. MSc, PhD/DPhil, Clinical) OR substantial equivalent experience.

Demonstrable experience of desk-based and qualitative and/or quantitative research and related technical skills.

Skilled at working in a remote environment and able to take ownership for seeing tasks and deliverables through to completion.

Demonstrable experience of psychometrics and related technical skills, including use of statistical software such as R or SAS.

Demonstrable experience in research related to patient reported outcomes, patient centered outcomes and clinical outcome assessments.

Excellent organizational, time management, and multi-tasking skills

Lead medical account management and planning with associated medical affairs functions for assigned national accounts

Serve as a technical resource for questions raised by Key Account Management and staff on Intercept products

Ability to work with individuals from diverse experiences, backgrounds, and levels of knowledge

Proactively share customer insights to help inform, advance, and support medical brand strategies, customer educational needs, health outcomes, and research priorities

Attend and support scientific, managed care, and medical meetings; prepare planned post-meeting deliverables

Minimum of 5 years of clinical orthotics and prosthetics experience

CPO, CP, or CO certification

Strong knowledge in clinical outcomes

Possess strong written and verbal communication skills

Strong knowledge of MS Office suite programs, expectation of routinely developing PowerPoint presentations

Develop and implement outcome-based programs

Knowledge of practical research implementation (IRB process, data collection and management) and qualitative and quantitative analysis

Fluency in English both orally and in writing, with excellent interpersonal skills.

Experience in a related field in academic or industry environment

Well-developed written and oral communication skills, including fluent English, both written and spoken

Perform background and targeted literature reviews as well as critiques of studies

Reviews or develops drafts of protocols and initial drafts of interview guides with limited direction

Database Entry And/or Management Experience, Preferred

Computer And Internet Skills And Experience, Required

Notifies appropriate institutional officials of external audits by FDA and sponsors.

Reviews and comprehends study protocols, Award Acceptance (contract Terms & Conditions).

Reviews and develops a familiarity with the protocol, e.g., study proceedings and timelines, inclusion and exclusion criteria, confidentiality, privacy protections.

Develops study timelines and implementation.