Lead Clinical Research Coordinator (2 Years Fixed Term)

🔍 School of Medicine, Stanford, California, United States

New

📁: Research

📅   : 1 day ago Post Date

📅   : 108854 Requisition #

Be at the Heart of Innovation.

Are you a clinical research professional looking for more than just a job? Do you thrive in an environment that feels like family but operates at the cutting edge of science? We are seeking a high-energy, experienced Lead Clinical Research Coordinator to join our Otolaryngology – Head and Neck Surgery (OHNS) department.

In this role, you won’t just manage protocols—you will be the central point of contact for a visionary team, bridging the gap between novel research and world-class patient care.

Why You’ll Love It Here

A "Big Picture" Opportunity: You will be at the forefront of novel research projects that span multiple divisions within OHNS. This is your chance to contribute to breakthroughs that change lives.
Family-Oriented Culture: We are a well-respected team that values the human side of medicine. We treat our staff like family, fostering a supportive, collaborative, and inclusive environment.
Empowered Leadership: As the center point of contact, you will exercise significant leadership skills, providing vital guidance to researchers and junior staff while ensuring the integrity of our most complex trials.

Your Impact

Central Liaison: Act as the primary coordinator and advisor for multidisciplinary research teams across various OHNS divisions.
Project Leadership: Provide expert guidance to researchers on protocol development, regulatory compliance (FDA/IRB), and study execution.
Advanced Coordination: Oversee the lifecycle of diverse, high-impact clinical trials, from initial setup and recruitment to data integrity and closure.
Mentorship: Serve as a leader and mentor, helping to train and develop the next generation of clinical research assistants and coordinators.

Your 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.

Please submit Cover Letter, Resume, and Letters of Reference (s), as applicable.

DESIRED QUALIFICATIONS:

Have a track record of successfully managing complex projects with many stakeholders.
Prior experience in clinical research working with Government and Industry Grants.
Deep understanding of ethical standards for human subject research.
Emotional intelligence to navigate a close-knit, family-oriented work culture while maintaining professional excellence.
A Bachelor of Science degree in biology, microbiology, health sciences, or nursing is desired.

EDUCATION & EXPERIENCE (REQUIRED):

Bachelor's 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.
May require a valid California Driver’s License.
Must possess and maintain a valid California non-commercial Class C Driver’s 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:

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.
When conducting university business, must comply with California Vehicle Code and Stanford University driving requirements.

The expected pay range for this position is $86,248 to $100,158 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 (https://cardinalatwork.stanford.edu/benefits-rewards) provides detailed information on Stanfordʼs 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