Clinical Research Coordinator Associate

Position: Clinical Research Coordinator Associate (2 vacancies)

Clinical Research Coordinator with project management skills for Parkinson’s disease Studies

Do you want to help Stanford University develop world-leading research to better diagnose and treat people suffering from Parkinson’s disease and Dementia with Lewy Bodies?

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 neurological and memory tests.
• Are a proven quick learner who doesn’t need hand holding to get started

Then we offer…

• The opportunity to contribute to understanding Parkinson’s disease and Dementia with Lewy Bodies
• 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. These studies collect information on memory and other mental abilities, which we link with brain imaging, biochemical and genetic markers, and autopsy results. Most research participants will have Parkinson’s disease, Dementia with Lewy Bodies, or another 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 to administer research questionnaires and administer psychometric tests.

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 online 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 see (Use the "Apply for this Job" box below)./

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.
• Coordinate collection of study specimens and processing.
• Collect and manage patient and laboratory 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.
• Assemble study kits for study visits, monitor scheduling of procedures and charges, coordinate documents, and attend monitoring meetings with sponsors, 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 patient and research data in appropriate files per institutional and…