Jobs
>
Stanford

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

    Stanford University
    Stanford University Stanford, United States

    1 day ago

    Default job background
    Description
    The Greicius Lab at Stanford University invites applications for a Clinical Research Coordinator.

    This will be a joint position in which applicants will have the opportunity to work alongside another Clinical Research Coordinator to gain research experience in genetics.

    Successful applicants will gain first-hand experience in data collection, processing, and analysis in a diverse laboratory setting. The Greicius Lab seeks to investigate neurodegenerative disorders with an emphasis on Alzheimer's Disease.

    We use genetics and neuroimaging methodologies to search for genetic variants that protect older healthy controls from developing Alzheimer's Disease or variants that increase the risk of developing Alzheimer's Disease in younger cases.

    We now have a dataset of 400+ long-read sequencing (LRS) genomes and are processing 500+ new African-ancestry long-read genomes, hoping to discover novel structural variants related to Alzheimer's Disease.

    The ideal candidate will have an interest in a variety of topics including genetics, biology, and different neurodegenerative diseases (i.e. Parkinson's Disease, Lewy Body Dementia).

    The Clinical Research Coordinator position entails the management of administrative responsibilities as well as hands-on involvement in research projects with a potential to contribute to publications.

    This position requires high attention to detail, excellent communication skills, and organizational prowess. Experience with data management, especially using REDCap, is strongly preferred. Knowledge of basic programming (i.e. Python, R) and the UNIX environment is ideal but not required. Bachelor's degree in Biomedical Engineering, Biology, Computer Science, Statistics, Physics, Neuroscience, Cognitive Neuroscience, Psychology, or related field is desirable. A minimum commitment of two years is highly desired.

    Interested candidates should email a cover letter and CV to Ilaria Stewart ), with "CRC Application" as the subject. Applicants should also be prepared to send in two letters of recommendation upon request.


    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 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.
    • Assemble study kits for study visits, monitor scheduling of procedures and charges, coordinate documents, and attend monitoring meetings with sponsors, acting as primary contact.
    • Monitor expenditures and adherence to 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.
    • Participate in monitor visits and regulatory audits.
    * - Other duties may also be assigned

    This is a fully on-site position.


    DESIRED QUALIFICATIONS:

    • Experience with data management, especially using RedCap is strongly preferred.
    • Knowledge of basic programming in Python and/or R and the UNIX environment is ideal but not required.
    • Bachelor's degree in Biomedical Engineering, Biology, Computer Science, Statistics, Physics, Neuroscience, Cognitive Neuroscience, Psychology, or related field desirable.

    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.

    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:
    Occasional evening and weekend hours.


    WORK STANDARDS:

    • Interpersonal Skills: Demonstrates the ability to work well with Stanford colleagues and clients and with external organizations.
    • Promote Culture of Safety: Demonstrates commitment to personal responsibility and value for safety; communicates safety concerns; uses and promotes safe behaviors based on training and lessons learned.
    • Subject to and expected to comply with all applicable University policies and procedures, including but not limited to the personnel policies and other policies found in the University's Administrative Guide,
    The expected pay range for this position is $27.88 to $36.54 per hour.


    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.

    At Stanford University, base pay represents only one aspect of the comprehensive rewards package. The Cardinal at Work website ) provides detailed information on Stanford's extensive range of benefits and rewards offered to employees. Specifics about the rewards package for this position may be discussed during the hiring process.

    Additional Information


    • Schedule: Full-time
    Job Code: 1013


    • Employee Status: Regular
    • Grade: F
    • Requisition ID: 102071
    • Work Arrangement : On Site


  • 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 ...


  • 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 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 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. 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

    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 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 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 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

    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

    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

    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 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 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

    Stanford University Clinical and Translational Research Program in the Heart Center at Lucille Packard Children's Hospital is seeking a Clinical Research Coordinator Associate (CRCA) to perform duties related to the coordination of clinical studies. The CRCA will coordinate moder ...


  • 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

    This is an exciting opportunity to join the Neuroscience Clinical Trials Team in Neurology & Neurosurgery. This team runs clinical trials for a wide range of disease areas including: Epilepsy, Neuorimmunology/Multiple Sclerosis, Alzheimers, Autonomic Disorders, Device Neurosurger ...


  • Stanford University Stanford, United States

    The Immune Behavioral Health (IBH) Research Program within the Division of Allergy, Immunology, Rheumatology in the Department of Pediatrics at Stanford University is seeking a Clinical Research Coordinator Associate (CRCA) to be appointed at 30 hours (.75% FTE) per week. Our pro ...