Jobs
>
Stanford

    Clinical Research Coordinator Associate - Stanford, United States - Stanford University

    Stanford University
    Stanford University Stanford, United States

    3 weeks ago

    Default job background
    Description

    The Department of Pediatrics, Division of Endocrinology is seeking a Clinical Research Coordinator Associate to perform duties related to the coordination of clinical studies.

    Coordinate moderately complex aspects of one or more clinical studies. Work under close direction of the principal investigator and/or study coordinator/supervisor.


    Duties include:

    • Serve as primary contact with research participants, sponsors, and regulatory agencies. Coordinate studies from startup through close-out.
    • Determine eligibility of and gather consent from study participants according to protocol. Assist in developing and implementing a variety of recruitment strategies.
    • Coordinate collection of study specimens and processing.
    • Collect and manage patient and laboratory data for clinical research projects. Manage research project databases, develop flow sheets and other study related documents, and complete study documents/case report forms.
    • Ensure compliance with research protocols, and review and audit case report forms for completion and accuracy with source documents. Prepare regulatory submissions and ensure institutional Review Board renewals are completed.
    • Conduct study visits and semi-structured interviews, monitor scheduling of procedures and charges, coordinate documents, and attend monitoring meetings with sponsors, acting as primary contact.
    • Assist in coding qualitative interviews, data-cleaning, and participating in the coding process.
    • Monitor expenditures and adherence to
    • Participate in monitor visits and regulatory study budgets and resolve billing issues in collaboration with finance and/or management staff.
    • Interact with the principal investigator regularly, ensuring patient safety and adherence to proper study conduct.
    • Ensure essential documentation and recording of patient and research data in appropriate files per institutional and regulatory requirements.
    * audits.
    * - Other duties may also be assigned


    Stanford University provides pay ranges representing its good faith estimate of what the University reasonably expects to pay for a position.

    The pay offered to a selected candidate will be determined based on factors such as (but not limited to) the scope and responsibilities of the position, the qualifications of the selected candidate, departmental budget availability, internal equity, geographic location and external market pay for comparable jobs.

    The hourly range for this position working in the California Bay area is between $31.73 to $36.54 based on commensurate experience and background.


    DESIRED QUALIFICATIONS:

    • Stanford IRB Knowledge
    • Assistant Clinical Research Coordinator experience

    EDUCATION & EXPERIENCE (REQUIRED):


    Two-year college degree and two years related work experience or a Bachelor's degree in a related field or an equivalent combination of related education and relevant experience.


    KNOWLEDGE, SKILLS AND ABILITIES (REQUIRED):

    • Strong interpersonal skills.
    • Proficiency with Microsoft Office.
    • Knowledge of medical terminology.
    • Previous use of RedCap (preferred not required)

    CERTIFICATIONS & LICENSES:
    Society of Clinical Research Associates or Association of Clinical Research Professionals certification is preferred.


    PHYSICAL REQUIREMENTS*:

    • Frequently stand, walk, twist, bend, stoop, squat and use fine light/fine grasping.
    • Occasionally sit, reach above shoulders, perform desk-based computer tasks, use a telephone and write by hand, lift, carry, push, and pull objects that weigh up to 40 pounds.
    • Rarely kneel, crawl, climb ladders, grasp forcefully, sort and file paperwork or parts, rarely lift, carry, push, and pull objects that weigh 40 pounds or more.
    * - Consistent with its obligations under the law, the University will provide reasonable accommodation to any employee with a disability who requires accommodation to perform the essential functions of his or her job.


    WORKING CONDITIONS:

    • Position may at times require the employee to work with or be in areas where hazardous materials and/or exposure to chemicals, blood, body fluid or tissues and risk of exposure to contagious disease and infections.
    • May require extended or unusual work hours based on research requirements and business needs.
    • Spanish speaking is preferred, as there will be monolingual Spanish participants in our studies.
    ~ All members of the Department of Pediatrics are engaged in continuous learning and improvement to foster a culture where diversity, equity, inclusion, and justice are central to all aspects of our work. The Department collectively and publicly commits to continuously promoting anti-racism and equity through its policies, programs, and practices at all levels. ~

    Additional Information


    • Schedule: Full-time
    Job Code: 1013


    • Employee Status: Fixed-Term
    • Grade: F
    • Department

    URL:

    • Requisition ID: 103036
    • Work Arrangement : Hybrid Eligible


  • Astranis San Francisco, United States

    Astranis is on a mission to bridge the digital divide by connecting the four billion people worldwide who currently lack internet access. We're doing this by building the next generation of smaller, more cost-effective spacecraft to bring the world online. · As a team, we've laun ...


  • Michaels Stores, Inc. San Mateo, United States

    Store - BAY-SAN MATEO, CA · Plan, coordinate, and facilitate events (including kids birthday parties) within a Michaels store to provide a stress-free, fun, and engaging experience for guests. Deliver friendly customer service by helping customers shop at our store and find what ...


  • Stanford University Stanford, United States

    Serve as primary contact with research participants, sponsors, and regulatory agencies. Coordinate studies from start-up through close-out. Determine eligibility of and gather consent from study participants according to protocol. Assist in developin Clinical Research, Research C ...


  • Stanford University Stanford, United States

    Serve as primary contact with research participants, sponsors, and regulatory agencies. Coordinate studies from start-up through close-out. Determine eligibility of and gather consent from study participants according to protocol. Assist in developin Research Coordinator, Clinica ...


  • Stanford University Stanford, United States

    Serve as primary contact with research participants, sponsors, and regulatory agencies. Coordinate studies from start-up through close-out. Determine eligibility of and gather consent from study participants according to protocol. Assist in developin Research Coordinator, Clinica ...


  • Stanford University Stanford, United States

    Serve as primary contact with research participants, sponsors, and regulatory agencies. Coordinate studies from startup through close-out. Determine eligibility of and gather consent from study participants according to protocol. Assist in developing Clinical Research, Research C ...


  • Stanford University Stanford, United States

    The Stanford Alzheimer's Disease Research Center (ADRC) recruits and follows older normal adults; older adults with mild cognitive impairment; and patients with Alzheimer's disease, Parkinson's disease, and related disorders. These studies collect in Clinical Research, Research C ...


  • Stanford University Stanford, United States

    Serve as primary contact with research participants, sponsors, and regulatory agencies. Coordinate studies from startup through close-out. Determine eligibility of and gather consent from study participants according to protocol. Assist in developing Clinical, Research, Associate ...


  • Stanford University Stanford, United States

    Serve as primary contact with research participants, sponsors, and regulatory agencies. Coordinate studies from start-up through close-out. Identify and implement changes to recruitment strategies when necessary. Determine eligibility of and gather c Clinical Research, Research C ...


  • Stanford University Stanford, United States

    Serve as primary contact with research participants, sponsors, and regulatory agencies. Coordinate studies from start-up through close-out. Determine eligibility of and gather consent from study participants according to protocol. Assist in developin Clinical Research, Research C ...


  • Stanford University Stanford, United States

    Serve as primary contact with research participants, sponsors, and regulatory agencies. Coordinate studies from startup through close-out. Determine eligibility of and gather consent from study participants according to protocol. Assist in developing Research Coordinator, Clinica ...


  • Stanford University Stanford, United States

    The Byers Eye Institute at Stanford University School of Medicine is seeking a Clinical Research Coordinator Associate to perform duties related to the coordination of clinical studies under the direction of Dr. Andrea Kossler, Associate Professor of Ophthalmology. Duties include ...


  • Stanford University Stanford, United States

    Clinical Research Coordinator for Cognitive Aging Studies Do you want to help Stanford University develop world-leading research to better diagnose and treat people suffering from Parkinson's disease and Alzheimer's disease? If you... Enjoy working d Clinical Research, Clinical, ...


  • Stanford University Stanford, United States

    Serve as the primary contact with research participants, sponsor, and regulatory agencies. Assist with the screening, recruiting, and obtaining consent of study participants. Review medical records and/or perform telephone or in-person interviews to Clinical Research, Research Co ...


  • Stanford University Stanford, United States

    The Department of Pediatrics, Division of Endocrinology is seeking a Clinical Research Coordinator Associate to perform duties related to the coordination of clinical studies. Coordinate moderately complex aspects of one or more clinical studies. Work under close direction of the ...


  • Stanford University Stanford, United States

    Serve as primary contact with research participants, sponsors, and regulatory agencies. Coordinate studies from start-up through close-out. Determine eligibility of and gather consent from study participants according to protocol. Assist in developin Research Coordinator, Clinica ...


  • Stanford University Stanford, United States

    Clinical Research Coordinator for Cognitive Aging, Dementia, and Parkinson's disease Do you want to help Stanford University develop world-leading research to better diagnose and treat people suffering from Parkinson's disease, Dementia with Lewy Bod Clinical Research, Research C ...


  • Stanford University Stanford, United States

    Duties include: · Serve as primary contact with research participants, sponsors, and regulatory agencies. Coordinate studies from startup through close-out. · Determine eligibility of and gather consent from study participants according to protocol. Assist in developing and imple ...


  • Stanford University STANFORD, United States

    The Byers Eye Institute at Stanford University School of Medicine is seeking a Clinical Research Coordinator Associate to perform duties related to the coordination of clinical studies under the direction of Dr. Andrea Kossler, Associate Professor of Ophthalmology. Duties include ...


  • Stanford University Stanford, CA, United States

    The Department of Anesthesiology, Perioperative, and Pain Medicine, at Stanford University's School of Medicine, is a world-leading department that offers comprehensive training and perioperative patient care, pain management, and critical care medicine as well as cutting-edge re ...