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Clinical Research Intern II
Clinical Research Intern IIThe Center for Orthopedic and Research E • Phoenix, AZ, US
Clinical Research Intern II

Clinical Research Intern II

The Center for Orthopedic and Research E • Phoenix, AZ, US
2 days ago
Job type
  • Full-time
Job description

Job Description

Job Description

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.

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