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    Clinical Research Coordinator - Philadelphia, United States - Proclinical

    Proclinical
    Proclinical Philadelphia, United States

    2 weeks ago

    Default job background
    Permanent Pharmaceutical / Bio-tech
    Description

    Clinical Research Coordinator - Philadelphia, PA - Permanent

    Proclinical is seeking a dedicated and enthusiastic Clinical Research Coordinator who is passionate about clinical-translational research in the field of head and neck cancer. This is a permanent position located in Philadelphia, PA.

    Primary Responsibilities:

    This role is ideal for someone interested in a career in science or medicine. The role will focus on three main areas: human biospecimen collection for research, updating a list of clinical trials relevant to head and neck malignancy, and serving other projects and infrastructure needs at the interface of clinical practice with head and neck cancer research.

    Skills & Requirements:

  • Bachelor of Science and relevant experience in clinical research compliance or auditing.
  • Excellent interpersonal, writing, and analytical skills.
  • Detail-oriented with excellent organizational and multitasking skills.
  • Ability to work independently and as part of a team.
  • Experience in oncology, REDCAP databases, specimen collection, and EPIC EMRs is desirable.The Clinical Research Coordinator will:
  • Support all aspects of human biospecimen collection for research from head and neck cancer patients.
  • Create and continuously update a list of clinical trials relevant to head and neck malignancy.
  • Serve other discrete projects and infrastructure needs at the interface of clinical practice with head and neck cancer research.
  • Manage study activities including subject recruitment, data entry, subject visits and follow-up, and regulatory documentation.
  • Interact directly with Principal Investigators, other lab members, research staff, and patients.
  • Adhere to all University of Pennsylvania, GCP/ICH, and FDA guidelines.
  • Screen, recruit, and consent potential study participants as specified per protocol.
  • Collect blood and other specimens and coordinate specimen storage and processing with various labs.
  • Complete CRFs and data entry to study databases, sample process and shipping, patient reimbursement, research billing review, etc.
  • Coordinate the administration of the investigational product and study related medications.
  • Maintain all study-related documents.
  • Prepare and participate in the conduct of audits by the study sponsors, CROs, the FDA, and other entities as required. If you are having difficulty in applying or if you have any questions, please contact Janelle Jones at (+1) or

    Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

    Proclinical Staffing is an equal opportunity employer.

    INDCR

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