Cancer Clinical Research Coordinator 2 - Melanoma (Hybrid)

Stanford University

Stanford, CA

JOB DETAILS
SALARY
$86,248–$101,158 Per Year
SKILLS
Adverse Events, Best Practices, Budget Management, Budgeting, Cancer, Clinical Laboratory, Clinical Research, Clinical Trial, Corrective Action, Customer Relationship Management (CRM), Data Analysis, Data Collection, Data Management, Detail Oriented, FDA (Food and Drug Administration), Hazardous Materials/Substances, Healthcare, IRB/IEC (Institutional Review Board/Independent Ethics Committee), Infectious Diseases, Interpersonal Skills, Investigational New Drug (IND), Investigator INDs, Laboratory Techniques, Leadership, Legal, Lift/Move 40 Pounds, Maintain Compliance, Material Moving, Medical Terminology, Medical Treatment, Medicine, Mentoring, Microsoft Office, Operational Audit, Organizational Skills, Patient Care, Pediatrics, Performance Analysis, Performance Reviews, Physical Demands, Policy Development, Policy Implementation, Recruiting Strategy, Regulatory Compliance, Research Laboratory, Research Skills, Risk, Safety/Work Safety, Schedule Development, Society of Clinical Research Associates (SoCRA), Staff Policies, Standards of Care, Systems Administration/Management, Team Lead/Manager, University/School Policies
LOCATION
Stanford, CA
POSTED
30+ days ago

Cancer Clinical Research Coordinator 2 - Melanoma Hybrid

The Stanford Cancer Institute (SCI) is one of an elite number of National Cancer Institute-Designated Comprehensive Cancer Centers in the country and is a prominent dynamic growing and complex Institute within the Stanford University School of Medicine. The SCI actively works to build synergies and collaborations among faculty with cancer-relevant expertise from four Schools and over 30 departments across Stanford University. We seek a Clinical Research Coordinator 2 to help us enact our mission to reduce cancer mortality through comprehensive cancer research treatment education and outreach.

Given the SCIs mission breadth and depth, it employs over 320 staff members in a fast-paced team-oriented and forward-thinking environment with tremendous opportunities for personal and professional growth. The Clinical Trial Office (CTO) is an integral component of the Stanford Cancer Institute. The vital work performed there enables our adult and pediatric cancer centers to translate research from the laboratory into the clinical setting.

You will be working with an unparalleled leading-edge community of faculty and staff who are fundamentally changing the world of healthcare in the cancer arena. Reporting to the Clinical Research Manager (CRM), the CRC2 will be conversant in the goals, mission, and priorities of the Institute and utilize this knowledge to ensure the safety and well-being of trial participants. We are seeking candidates with excellent interpersonal skills and attention to detail.

Our staff run toward challenges, and you will have a demonstrated history of doing the same with a high degree of professionalism, initiative, and flexibility.

Job Summary

Stanford University is seeking a Clinical Research Coordinator 2 to conduct clinical research and work independently on progressively more complex projects/assignments for our Melanoma Clinical Research Group (CRG).

Key Responsibilities

  • Independently manage significant and key aspects of a large study or all aspects of one or more small research studies.
  • This includes managing Tumor-Infiltrating Lymphocyte studies that include inpatient stays with complex treatment.
  • 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, 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 (IRB) submissions and respond to requests and questions. • Collaborate with principal investigators and study sponsors to monitor and report serious adverse events and resolve study queries. • Provide leadership in determining recommending and implementing improvements to policies and 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 documents to ensure ongoing regulatory compliance. • Work with principal investigator to ensure Investigational New Drug (IND) applications are submitted to the FDA when applicable. • Ensure IRB renewals are completed.

Requirements

  • 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

  • Strong interpersonal skills.
  • Proficiency with Microsoft Office and database applications.
  • Experience with research protocols and regulatory or governing bodies, including 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.

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.

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

  • 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 (http://adminguide.stanford.edu).

Salary and Benefits

The expected pay range for this position is $86,248 to $101,158 per annum. Stanford University provides pay ranges representing its good faith estimate of the salary or hourly wage the university reasonably expects to pay for a position upon hire. 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 (http://cardinalatwork.stanford.edu/benefits-rewards) 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.

About the Company

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Stanford University