Clinical Research Intern II

Healthcare Outcomes Performance Company

Job Location:

Phoenix, NM - USA

Monthly Salary: Not Disclosed

Posted on: 30-10-2025

Vacancies: 1 Vacancy

Job Summary

ESSENTIAL FUNCTIONS

Assist in the design data collection and organization of ongoing retrospective and prospective orthopaedic clinical studies.
Support manuscript writing literature review and reference management for ongoing and new publications in arthroplasty sports medicine spine and other musculoskeletal disciplines.
Collaborate with multidisciplinary teams including data scientists research coordinators and principal investigators.
Conduct basic data analysis prepare summary tables and figures and assist with IRB submissions or protocol amendments as appropriate.
Participate in regular research team meetings and contribute to abstract and presentation preparation for national orthopaedic meetings.

EDUCATION

MD or equivalent degree in medicine with training or background in orthopaedic surgery.

EXPERIENCE

Demonstrated interest in clinical research and scholarly publication.
Strong written and verbal communication skills in English.
Proficiency in Microsoft Office (Word Excel PowerPoint); familiarity with REDCap EndNote or statistical software (e.g. JMP SPSS R) preferred but not required.
Ability to work both independently and collaboratively in a fast-paced research environment

REQUIREMENTS

Eligibility to participate in a visiting research internship or observership in the U.S.
Demonstrated academic interest in orthopaedic outcomes research musculoskeletal innovation or related fields.
Excellent written and spoken English communication skills.

KNOWLEDGE

Foundational understanding of clinical study design including retrospective chart review and prospective registry-based studies.
Awareness of orthopaedic surgical terminology procedures and outcomes measures (e.g. PROMs complications revisions).
Basic knowledge of data management and ethics in human subjects research (HIPAA IRB GCP).
Familiarity with academic publishing standards reference citation tools (e.g. EndNote Zotero) and manuscript formatting.
Understanding of Microsoft Office applications and online collaboration platforms (e.g. Box SharePoint or Google Workspace).

SKILLS

Strong scientific writing and editing skills with attention to accuracy clarity and structure.
Excellent data organization and analytical abilities including interpretation of clinical outcomes and research metrics.
Proficiency in conducting literature searches and managing references using EndNote Mendeley or similar tools.
Effective communication and interpersonal skills to collaborate with multidisciplinary research teams.
Strong time management and project coordination skills to meet deadlines across multiple studies

ABILITIES

Ability to apply critical thinking and problem-solving skills to clinical research questions.
Ability to maintain strict confidentiality when handling protected health information (PHI) and study data.
Ability to work independently with minimal supervision while maintaining responsiveness to team feedback.
Ability to adapt to shifting priorities and manage multiple concurrent projects.
Ability to present findings in oral or written form including contributions to manuscripts and conference abstracts.

ENVIRONMENTAL WORKING CONDITIONS

Work performed primarily in an office or research setting with occasional time spent in clinical environments (e.g. orthopaedic clinics operating rooms) for data collection or observation.
Exposure to standard office equipment (computers printers scanners etc.) and secure electronic data systems.
Minimal exposure to patient care areas; no direct clinical responsibilities.
Work hours typically follow a standard weekday schedule though flexibility may be required for meetings or deadlines across time zones.
Collaboration with remote team members through secure digital platforms (Box REDCap Microsoft Teams Zoom etc.).

PHYSICAL/MENTAL DEMANDS

Prolonged periods of sitting and computer use required for data entry writing and virtual meetings.
Occasional walking or standing when conducting chart reviews or collecting clinical data onsite.
High level of mental focus and attention to detail required for data accuracy and literature review.
Ability to manage competing priorities and adhere to project deadlines.
Strong commitment to academic integrity professionalism and continuous learning.

ORGANIZATIONAL REQUIREMENTS

HOPCo Mission Vision and Values must be acknowledged and adhered to
Completion of Human Subjects Ethics in Research (i.e. CITI training) and other assigned learning modules prior to independent study participation.

This description is intended to provide only basic guidelines for meeting job requirements. Responsibilities knowledge skills abilities and working conditions may change as needs evolve.

Required Experience:

Intern

ESSENTIAL FUNCTIONSAssist in the design data collection and organization of ongoing retrospective and prospective orthopaedic clinical studies.Support manuscript writing literature review and reference management for ongoing and new publications in arthroplasty sports medicine spine and other muscul...