Job description

Requirements

  • Entry level
  • No Education
  • Salary to negotiate
  • CALIFORNIA US

Description

Clinical Research Coordinator Associate�School of Medicine, Stanford, California, United StatesNew�Research�1 day ago Post Date�85378 Requisition #The Clinical Research Coordinator Associate is responsible for the overall implementation of an assigned set of research protocols assuring efficiency and regulatory compliance. These studies will be conducted at the Stanford Hospital and Clinics. The CRCA will work as part of a clinical trials research team and report to the Clinical Research Manager and various Principal Investigators conducting clinical research within the Stanford Stroke Center’s Stroke Recovery Program. The primary responsibilities will include administration of neuropsychological tests and processing of study specimens. Other significant responsibilities will include recruiting, screening, acquiring informed consent and enrolling subjects in accordance with good clinical practice guidelines; collect, record and maintain complete data files using good clinical practice in accordance with HIPAA regulations. He/she participates in data retrieval, reporting, and preparation of files and Case Report Forms for the various studies. The successful candidate will feel comfortable interacting, recruiting, and completing study procedures with study participants the hospital and/or clinical setting.

Duties include:

- Significant time will be spent administering neuropsychological testing and processing study specimens (primarily blood).
- Determine eligibility of and gather consent from study participants according to protocol. Assist in active recruitment or study participants and continued developing recruitment strategies.
- Coordinate and schedule study visits.
- Serve as primary contact with research participants, sponsors, and regulatory agencies. Coordinate studies from startup through close-out.
- 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, prepare regulatory submissions and institutional Review Board renewals.
- Assemble study kits for study visits, prepare study documents for data collection
- 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.

* - Other duties may also be assigned
DESIRED QUALIFICATIONS:

- 1+ years of Clinical Research Coordinator experience.
- Extensive experience with patient recruitment in a clinical setting.
- Experience with administering neuropsychological tests.
- Experience with longitudinal studies and/or investigator-initiated studies.
- Fluency in Spanish is desirable but not a requirement.

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, http://adminguide.stanford.edu.

Additional Information
- Schedule: Full-time
- Job Code: 4924
- Employee Status: Regular
- Grade: F
- Department URL: http://med.stanford.edu/neurology/
- Requisition ID: 85378

  • education
  • ms project
  • protocol
  • recruitment
  • spanish