Clinical Research Coordinator Associate (2-Year Fixed Term)

Stanford University

Stanford, CA

JOB DETAILS
SALARY
$34.56–$40.30 Per Hour
SKILLS
Budgeting, Cancer, Case Report Form (CRF), Clinical Research, Clinical Trial, Clinical Trial Management, Communication Skills, Computer Skills, Customer Support/Service, Data Management, Database Administration, Database Programming, Detail Oriented, Disability Accommodations, Documentation, Follow Through, Funding, Healthcare, IBM SPSS Statistical Package, IRB/IEC (Institutional Review Board/Independent Ethics Committee), Interpersonal Skills, Legal, Lift/Move 40 Pounds, Maintain Compliance, Material Moving, Medical Research, Medicine, Microsoft Office, Organizational Skills, Patient Safety, Physical Demands, Presentation/Verbal Skills, Project/Program Management, Psychiatry and Mental Health, Qualitative Research, Recruiting Strategy, Regulations, Regulatory Requirements, Regulatory Submissions, Society of Clinical Research Associates (SoCRA), Staff Policies, Startup, Strategic Planning, Writing Skills
LOCATION
Stanford, CA
POSTED
30+ days ago

The Department of Psychiatry and Behavioral Sciences at Stanford Universitys School of Medicine is looking for an organized and motivated individual to fill the role of Clinical Research Coordinator Associate (CRCA) to coordinate aspects of a study focusing on fertility and family building in young adult female cancer survivors. This role involves interacting with healthcare professionals, research participants, and study collaborators, so candidates must possess strong interpersonal skills. The CRCA will interact daily with the clinical research manager and the PI to ensure adherence to the project protocol and will attend weekly project meetings with the PI and senior staff. Work will be delegated amongst the research staff for efficiency so candidates must be able to work effectively independently and with others. This is a fixed-term appointment, with funding currently available through August 31, 2028 with a possibility of an extension.

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.

Collect and manage patient 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.

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
    • 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.

DESIRED QUALIFICATIONS:

Bachelors Degree in a related field.

Experience with recruitment of research participants for clinical studies.

Qualitative research experience preferred.

Ability to follow through and complete assigned tasks.

Strong organizational skills and attention to detail.

Strong verbal and written communication skills.

Excellent customer service and interpersonal skills.

Basic computer skills and demonstrated experience with office software and email applications.

Familiarity with REDCap is a plus (but not a requirement).

Familiarity with SPSS is a plus (but not a requirement).

Familiarity with EPIC is a plus (but not a requirement).

EDUCATION & EXPERIENCE (REQUIRED):

Two-year college degree and two years related work experience or a Bachelors 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 and research 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.

This work arrangement will be primarily remote; however, the Clinical Research Coordinator Associate will be required to be onsite once a week for in-person meetings.

This role is open to candidates anywhere in the United States. The compensation for this position will be based on the location of the successful candidate.

The expected pay range for this position is $34.56 to $40.30 per hour.

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 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.

WORK STANDARDS (from JDL)

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.

    • 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.

Additional Information

  • Schedule: Full-time
  • Job Code: 1013
  • Employee Status: Fixed-Term
  • Grade: F
  • Requisition ID: 109169
  • Work Arrangement : Remote Eligible

About the Company

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Stanford University