Clinical Research Scientist - Neuropsychology

PAVIR•Stanford, CA

4d•Onsite

About The Position

Palo Alto Veterans Institute for Research (PAVIR) is seeking a part-time Clinical Research Scientist. The position is for a Clinical Research Scientist to provide training and mentorship of study staff. The Research Scientist will also participate in manuscript preparation and dissemination (e.g., presentation) of research findings. This is a part-time, 10 hours/week, position, located in Palo Alto, CA.

Requirements

Master's or Ph.D
Valid Driver License required
1 year or more of neuropsychological assessment experience
Good understanding of clinical terminology and procedures gained through experience
Experience with research protocols and regulatory or governing bodies, which include HIPAA and FDA regulations, Institutional Review Board requirements, and Good Clinical Practices
Ability to read and understand study/trial protocol
Ability to prioritize and organize a high-volume workload and adapt to changing priorities
Demonstrated ability to work independently and cooperatively
Demonstrated ability to work and communicate effectively with study subjects
Proven track record towards meeting goals and deadlines
Strong interpersonal skills
Proficiency with Microsoft Office and database applications

Nice To Haves

Degree in a related field.
Previous experience in a clinical and research environment
Experience with grants and contract's function, clinical trial and research data management
Knowledge of VA and its health care system regarding clinical research trials and understanding of VA procedures and safety regulations
Knowledge of and experience working in orthopedic research
Knowledge of medical terminology.

Responsibilities

Responsible to the local Site Investigator of the research trial.
Works directly with site investigator(s), study coordinator and other facility staff. Responsible for mentorship and training of pertaining to the administration and scoring of clinical intakes and study-related assessments
Maintains a high level of knowledge and understanding of the study protocol, including all requirements for patient visits, obtaining informed consent, patient visit schedules, test procedures
Prepares and disseminates training materials for study staff pertaining to the administration and scoring of clinical intakes and study-related assessments
Requires knowledge of good clinical practices as well as the ability to work independently.
Fosters collaborative research relationships using excellent communication and interpersonal skills with investigators and participants.
Interact with Site Investigator as needed to ensure patients receive appropriate medical and psychiatric evaluation and care when needed, and alerts Site Investigator of adverse events when appropriate
Other tasks as assigned.