Research Assistant Jobs

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Clinical Research Assistant Division of Emergency Medicine Part Time

Children's Hospital of Philadelphia•Philadelphia, PA
•$21 - $26•Onsite

About The Position

The Division of Emergency Medicine at Children’s Hospital of Philadelphia is seeking a part-time Clinical Research Assistant to join a research team conducting clinical research at its Philadelphia location. The team focuses on social, biological, and environmental determinants of children’s health across the continuum of emergency care, from prevention to recovery. Under the supervision of the Program Manager and Associate Director of Research Operations, the assistant coordinates clinical research activities within specific study protocols and under the guidance of the study principal investigator and Program Manager. Duties include recruiting and enrolling participants, entering data, and following up with participants as required by study protocols. The role may also involve human-subject research activities such as data and sample collection and support for regulatory submissions.

Requirements

  • High school diploma or GED.
  • Previous relevant clinical research experience.
  • Familiarity with IRB processes and human-subject protection.

Nice To Haves

  • Bachelor's degree.
  • At least one year of relevant clinical research experience.

Responsibilities

  • Provide technical and administrative support in conducting clinical research.
  • Schedule patients or research participants.
  • Screen participants for inclusion and exclusion criteria or obtain case history.
  • Collect, enter, and manage data.
  • Process laboratory samples.
  • Perform clinical research study procedures or administer questionnaires.
  • Organize research records and study-related documentation.
  • Adhere to IRB-approved protocols, HIPAA requirements, and practices for handling confidential materials.
  • Comply with institutional policies, standard operating procedures, guidelines, and federal, state, and sponsor policies.
  • Recruit and enroll research participants and follow up with them as required by study protocols.
  • With appropriate authorization and training, obtain participant consent.
  • Document and report adverse events.
  • Maintain study source documents and complete case report forms or other study documentation using paper or electronic data capture.
  • Assist with IRB and regulatory submissions.
  • Provide follow-up care.
  • Order materials and supplies.
  • Schedule research meetings.

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