Under the direction of the Administrative Director of the Clinical Research Unit and in consultation with the Principal Investigator, the Data Manager will assist in the coordination of all research activities related primarily to the Neuro-Oncology Program at UCLA. You are responsible for ensuring that protocol procedures have been completed accurately, safely, and in a timely manner. This includes but is not limited to: responsibility for data collection, researching chart documentation, maintaining quality assurance, maintaining drug records, reporting preparation protocol information and disseminating to health care professionals, patients, and their family members.QualificationsREQUIRED
Clinical research experience with
in-depth knowledge of clinical oncology.
Working knowledge of good clinical practices for clinical research.
Ability to work efficiently and complete tasks with a high degree of accuracy.
Ability to organize and solve problems for efficiency and cost effectiveness.
Ability to work and solve problems with minimal supervision.
Ability to multi-task and prioritize effectively.
Ability to be flexible in handling work delegated by more than one individual.
Strong interpersonal communication skills to effectively and diplomatically
interact with others.
Strong written communication skills.
Experience in patient-related policies and procedures in university-wide, state
and federal regulatory management of clinical trials.
Skill in organizing and maintaining accurate, up-to-date files and records for
audits and other follow up activities.
Ability to lift up to 25 lbs
A Bachelor's Degree in the
biological/health sciences or related field from an accredited university
UCLA is an Equal Opportunity/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, or protected Veteran status.[Register to View] />