Assistant Clinical Research Coordinator

at  Stanford University

The Division of Cardiovascular Medicine, in the Department of Medicine, is a dynamic and innovative center dedicated to excellence in research, medical education, and clinical care. Our division is driven by over 80 faculty, clinician educators and instructors who are the pillar of strength in the Division’s ongoing efforts in the prevention and treatment of cardiovascular disease.
Under the supervision of the Clinical Research Manager and the Principal Investigator, the incumbent is responsible for coordinating clinical trials in the Interventional Cardiology Department. The incumbent is responsible for the timely and accurate collection and coordination of data submission to study sponsors ensuring quality control and leading to timely milestone payments. This includes responsibility for the compilation and transcription of research patient data and study-related information into case report forms (CRFs) into sponsor specific electronic data capture systems (EDC). S/he will work with the clinical research team to manage and collect accurate data and assist Principal Investigators and study coordinators for all data management aspects of their clinical trials. The incumbent is also responsible for maintaining communication with all elements of a multi-level research network, interacting with sponsoring agencies and compliance and regulatory groups such as the Institutional Review Board (IRB), Food and Drug Administration (FDA), and sponsor monitors. In addition, this individual must accurately maintain clinical trial information in the clinical trial management system (OnCore) and adhere to institutional policies.
As an Assistant Clinical Research Coordinator, you’ll play a key role in supporting the management and coordination of clinical trials and research studies. Working closely with senior team members, you’ll help organize tasks, meet deadlines, and ensure compliance with study protocols and regulations. This position offers hands-on experience in a dynamic research environment where your contributions will directly impact the success of clinical projects.

DESIRED QUALIFICATIONS:

• Experience with clinical research. Knowledge with various types of human subject clinical trials i.e., Industrial, and Investigator-authored.
• Experience with clinical trial management systems, electronic data capture and OnCore.

EDUCATION & EXPERIENCE (REQUIRED):

• Two-year college degree and one year of relevant experience or an equivalent combination of experience, education, and training.

KNOWLEDGE, SKILLS AND ABILITIES (REQUIRED):

• General knowledge of medical terminology.

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.

DUTIES INCLUDE:

• Schedule and/or call subjects for appointments; contact participants with reminders or other requirements.
• Prepare, distribute, and process questionnaires.
• Perform clerical duties in the preparation of regulatory documents. Maintain all forms and documents, including consent forms and master subject logs. File all appropriate correspondence.
• Assist with the screening, recruiting, and obtaining consent of study participants. Review medical records and/or perform telephone or in-person interviews to gather data, as needed.
• Administer standard study questionnaires and tests, score test measurements and questionnaires, and code data for computer entry. Perform quantitative review of forms, tests, and other measurements for completeness and accuracy.
• Extract data from source documents for research studies as directed. Collect data and complete case report forms.
• Perform basic measurements and tests on patients according to protocol, such as obtaining vital signs and performing phlebotomy and EKG, after appropriate training/certification. Collect study specimens according to protocol.
• Prepare, process, and ship specimens/samples accurately under well-defined requirements.
• Order and maintain equipment and supplies.
• Process study compensation payments and thank you letters to subjects upon completion of trial activities. Assist with post-study activities, as needed.

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://cardinalatwork.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.