Job Information
Stanford University Clinical Research Coordinator Associate in Stanford, California
Clinical Research Coordinator Associate
School of Medicine, Stanford, California, United States
New
Research
Post Date 2 days ago
Requisition # 103783
Clinical Research Coordinator with project management skills for research on healthy aging, Parkinson’s disease, and aging with HIV infection.
Do you want to help develop world-leading research to better diagnose and treat older adults with HIV infection, older adults with cognitive impairment, or adults with neurological impairment (e.g., Parkinson’s disease)?
If you…
Enjoy working directly with patients and their families.
Are exceptionally organized and can balance multiple projects at one time.
Love learning new skills, such as how to administer neuropsychological tests and motor exams, and how to assess sleep, as well as learning Magnetic Resonance Imaging (MRI) data acquisition skills.
Are a proven quick learner who doesn’t need handholding to get started.
Then we offer…
The opportunity to contribute to understanding aging and decline in HIV infection, Parkinson’s disease, and related disorders.
Challenging but positive environment where you will always learn new things.
Teamwork and camaraderie.
Competitive full-time salary.
Excellent Stanford benefits.
The Poston Lab recruits and follows older normal adults; older adults with mild cognitive impairment; and patients with Parkinson’s disease, Dementia with Lewy Bodies, and related disorders. We are looking for a Clinical Research Coordinator on a project that focusses on healthy aging, Parkinson’s disease, and aging with HIV infection. All these studies collect information on cognition, memory, and other mental abilities, which we link with brain imaging, sleep, brain imaging, and biochemical results. Research participants will have Parkinson’s disease, treated HIV infection, or another age-related neurodegenerative disorder; some participants will not have any impairment.
The Poston Lab seeks a full-time Clinical Research Coordinator Associate. The desired candidate has excellent project management skills and ability to coordinate between multiple teams, is self-motivated, detail-oriented, relatively independent, patient, punctual, and conscientious, with excellent interpersonal skills and excellent communication skills in English. Preference will be given to qualified candidates, who are also native/fluent in Spanish (written and verbal). Under the supervision of Dr. Poston and other study investigators, main duties include project management and coordination between interdisciplinary teams, in-person and telephone recruitment of research participants; obtaining informed consent; scheduling and coordination of research participant visits; maintaining longitudinal contact with participants by phone, email and other means; data collection (including psychometric data), scoring, and data entry. Training will be provided, for example, to administer research questionnaires, psychometric tests, and motor exams, and to acquire sleep assessments and MRI scans.
We like working with other smart, motivated, fun people looking to better the lives of our patients through scientific discovery. In addition to submitting your on-line resume, please include a cover letter describing your project management and/or clinical research experience and the top five attributes or experiences that make this the right job for you. For more information about our lab and research, please seehttp://neurology.stanford.edu/labs/postonlab/
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 with recruitment strategies.
Coordinate collection of study specimens and processing.
Collect and manage study participant, MRI, sleep, and laboratory data for 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.
Assemble study kits for study visits, monitor scheduling of procedures and charges, coordinate documents, and attend regular meetings with senior staff/principal investigator, acting as primary contact.
Monitor expenditures and adherence to study budgets and resolve billing issues in collaboration with finance and/or management staff.
Interact with the principal investigator regularly, ensuring patient safety and adherence to proper study conduct.
Ensure essential documentation and recording of participant and research data in appropriate files per institutional and regulatory requirements.
Participate in monitor visits and regulatory audits.
* - Other duties may also be assigned
This position is fully-onsite.
DESIRED QUALIFICATIONS:
Excellent verbal and written communication skills in English required.
Excellent verbal and written communication skills in Spanish desired.
Prior experience with patients or research subjects is desired. Preference given to applicants with previous experience, particularly clinical research experience with older adults who may be living with HIV infection, may have neurological impairment (e.g., Parkinson’s disease) or cognitive impairment (e.g., mild cognitive impairment, Alzheimer’s disease).
Ability to communicate clearly and empathetically with research participants and their families.
Strong interpersonal skills, including the ability to work easily with research participants and research team members.
Strong general computer skills and ability to quickly learn and master computer programs.
Strong analytical skills and experience with computer spreadsheets and database software, e.g., RedCap.
Proficiency with Microsoft Office and Excel.
Ability to work under deadlines with general guidance.
EDUCATION & EXPERIENCE (REQUIRED):
BA/BS required; major in neuroscience, psychology, or the biological sciences preferred (equivalent combination of skills, education, and experience will be considered.)
New graduates are encouraged to apply.
KNOWLEDGE, SKILLS AND ABILITIES (REQUIRED):
Strong interpersonal skills within a team environment and with study participants.
Experience in organizing and implementing multiple complex tasks.
Comfort with data collection using a variety of computer interfaces.
Attention to detail.
Experience with computer programs, such as Microsoft Office Word, Excel, REDCap, and/or other computer interfaces preferred.
An understanding of the principles of sound research design and data collection is an advantage.
Knowledge of medical terminology.
CERTIFICATIONS & LICENSES:
None required. 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.
The expected pay range for this position is $31.73 to $36.54 per hour.
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 (https:/lcardinalatwork.stanford.edu/benefits-rewards) provides detailed information on Stanford's 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 at
stanfordelr@stanford.edu. For all other inquiries, please submit acontact 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
Schedule: Full-time
Job Code: 1013
Employee Status: Regular
Grade: F
Requisition ID: 103783
Work Arrangement : On Site