Skip Navigation

Search all jobs

Let’s change the world together!

USC is a leading private research university located in Los Angeles – a global center for arts, technology and international business. As the city’s largest private employer, responsible for more than $5 billion annually in economic activity in the region, we offer the opportunity to work in a dynamic and diverse environment, in careers that span a broad spectrum of talents and skills across a variety of academic schools and units. As a USC employee, you will enjoy excellent benefits and perks, and you will be a member of the Trojan Family - the faculty, staff, students and alumni who make USC a great place to work. Think you’ve got what it takes to join us? We invite you to search our open positions and apply!

Program Administrator - Medical Monitor

USC Alzheimer's Therapeutic Research Institute San Diego, California

The USC Keck School of Medicine - Alzheimer Therapeutic Research Institute (ATRI), located in San Diego, California is an academic institute comprised of an expert panel of scientific collaborators committed to advancing the development of new treatments for Alzheimer’s Disease (AD) through innovative clinical trials.

Incumbent will provide oversight to the progress of clinical trials at study sites, and ensure that they are conducted, recorded, and reported in accordance with the protocol, Standard Operation Procedures (SOPs), Good Clinical Practice (GCP), and the applicable regulatory requirements(s).  Duties will include but are not limited to:

  • Supports study design, generation of study protocol, CRF, informed consent, and other study material.
  • Provides continuous medical monitoring during study conduct, answers site questions on inclusion/exclusion criteria or other protocol questions, evaluates and assesses SAEs and AEs, reviews laboratory and other safety parameters, reviews patient profiles, reviews coded terms for medical history, concomitant medications, adverse events, and provides medical expertise to project teams during course of study.
  • Provides therapeutic training relevant to specific study to the project team.
  • Attends and/or presents at investigator, internal and external project team meetings.
  • Defines criteria for protocols, assesses and evaluates protocol deviations and recommends on actions to be taken.
  • Provides medical insight on ethical, e.g. medical, aspects of study.
  • Contributes to discussions with investigators, opinion leaders, internal and external clients.
  • Provides benefit/risk evaluations and drug safety expertise for drugs.
  • Contributes to and reviews Safety Management Plans, Medical Monitoring Plans, Pharmacovigilance Plans, Risk Management Plans including design and conduct of safety studies.
  • Evaluates spontaneous reports and literature cases.
  • Communicates with reporting site investigators and site staff regarding medical and safety issues.
  • Evaluates safety issues in protocols and provides feedback to sites and study teams.

Location:  San Diego, CA

Salary is dependent on education and experience.

Minimum Education: Bachelor's degree, Combined experience/education as substitute for minimum education

Minimum Experience: 3 years

Minimum Field of Expertise: Directly related professional experience in area of program specialization.

REQ20052973 Posted Date: 11/09/2017 - Thru date - 12/31/2017

Job matching

With just one click and a connection to LinkedIn, we can connect you with jobs that match your work experience.

Start matching

Stay connected with University of Southern California

Sign up to receive job alerts

Select interests

Recently added jobs