Clinical Research Coordinator 2

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profile Job Location:

Redwood City, CA - USA

profile Yearly Salary: $ 86248 - 100158
Posted on: Yesterday
Vacancies: 1 Vacancy

Job Summary

The Department of Orthopaedic Surgery is seeking a Clinical Research Coordinator 2 (CRC2) to conduct clinical research and manage the clinical research studies with Trauma Services which specializes in orthopaedic trauma surgery and treating all aspects of fractures of the upper extremity (except the hand) lower extremity and pelvis as well as nonunions and malunions. This position independently assigns trial workload and manages performance through coaching and supervision of Clinical Research Coordinator Associate Med. Students Med scholars Residents Fellows and Post-docs. The CRC2 for Trauma reports to the Chief of Orthopaedic Trauma and serves as the resourcing lead and supervisor to assure project needs are adequately met and assigns adequate coverage for workload trials. The desired candidate is detail-oriented and conscientious with excellent written and oral communication and interpersonal skills. To learn more about the department please visit us at: .

Duties include*:

  • Oversee subject recruitment and study enrollment goals. Determine effective strategies for promoting/recruiting research participants and retaining participants in long-term clinical trials.
  • Oversee data management for research projects. Develop and manage systems to organize collect report and monitor data collection. Extract analyze and interpret data.
  • Develop project schedules targets measurements and accountabilities as assigned. Lead team meetings and prepare/approve minutes.
  • Formally supervise train and/or mentor new staff or students as assigned potentially including hiring preparing or assisting with the preparation of performance evaluations and performing related duties in addition to instruction on project work.
  • Audit operations including laboratory procedures to ensure compliance with applicable regulations; provide leadership in identifying and implementing corrective actions/processes. Monitor Institutional Review Board submissions and respond to requests and questions.
  • Collaborate with principal investigators and study sponsors monitor and report serious adverse events and resolve study queries.
  • Provide leadership in determining recommending and implementing improvements to policies/processes; define best practices.
  • Develop study budget with staff and principal investigator identifying standard of care versus study procedures. Track patient and study specific milestones and invoice sponsors according to study contract.
  • Ensure regulatory compliance. Regularly inspect study document to ensure ongoing regulatory compliance.
  • Work with principal investigator to ensure Investigational New Drug applications are submitted to the FDA when applicable. Ensure Institutional Review Board renewals are completed.

* - Other duties may also be assigned.

EDUCATION & EXPERIENCE (REQUIRED):

Bachelors degree in a related field and two years of experience in clinical research or an equivalent combination of education and relevant experience.

KNOWLEDGE SKILLS AND ABILITIES (REQUIRED):

  • Strong interpersonal skills.
  • Proficiency with Microsoft Office and database applications.
  • Experience with research protocols and regulatory or governing bodies which include HIPAA and FDA regulations Institutional Review Board requirements and Good Clinical Practices.
  • Knowledge of medical terminology.

CERTIFICATIONS & LICENSES:

  • Society of Clinical Research Associates or Association of Clinical Research Professionals certification is preferred.
  • Must possess and maintain a valid California non-commercial Class C Drivers License.

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.
  • Ability to drive day or night.

* - 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 diseases and infections.
  • May require extended or unusual work hours based on research requirements and business needs.

WORK STANDARDS:

  • When conducting university business must comply with California Vehicle Code and Stanford University driving requirements.
  • 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 Universitys Administrative Guide .

The expected pay range for this position is $86248 to $100158 per annum.

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 Stanfords extensive range of benefits and rewards offered to employees. Specifics about the rewards package for this position may be discussed during the hiring process.

Consistent with its obligations under the law the University will provide reasonable accommodations to applicants and employees with disabilities. Applicants requiring a reasonable accommodation for any part of the application or hiring process should contact Stanford University Human Resources by submitting a contact form.

Stanford is an equal employment opportunity and affirmative action employer. All qualified applicants will receive consideration for employment without regard to race color religion sex sexual orientation gender identity national origin disability protected veteran status or any other characteristic protected by law.

The job duties listed are typical examples of work performed by positions in this job classification and are not designed to contain or be interpreted as a comprehensive inventory of all duties tasks and responsibilities. Specific duties and responsibilities may vary depending on department or program needs without changing the general nature and scope of the job or level of responsibility. Employees may also perform other duties as assigned.

Additional Information

Required Experience:

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The Department of Orthopaedic Surgery is seeking a Clinical Research Coordinator 2 (CRC2) to conduct clinical research and manage the clinical research studies with Trauma Services which specializes in orthopaedic trauma surgery and treating all aspects of fractures of the upper extremity (except th...
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The Department of Orthopaedic Surgery is seeking a Clinical Research Coordinator 2 (CRC2) to conduct clinical research and manage the clinical...

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