Public Administration Analyst

Hi

Hope you are doing great.

I am Pradeep Singh with SDK (Siri Info Solutions). Siri Info Solutions is a staffing firm with a heritage of over 16 years partnership with Fortune 500 clients globally.

We have an immediate opening for a position of Public Administration Analyst in Los Angeles CA with one of our premium clients. If you are available and interested please send me your updated resume and if you have any further questions please feel free to reach me at .

Job Title: Public Administration Analyst

Location: Los Angeles CA

Assignment: 4month assignment with possible extension

Shift: 8:00 am to 5:00 pm with break times

Note: Specialized position that will be able to hit the ground running with previous experiences in clinical trial coordination

Experience:

• Study Coordinator Clinical Manager Clinical Research Associate Clinical Research Associate Clinical Research Regulatory

Skills:

• Attention to detail analytical organized interpersonal communication multitasking.

Location:

• Currently oncampus (Westwood CA) and travel as needed.

Schedule:

• MondayFriday. 8 am 5 pm.

Job Duties

The Department of Medicine Clinical Trial Program is seeking a skilled Clinical Research Associate to oversee manage and participate in research activities. Providing oversight of clinical research sites compliance with ICH/Good Clinical Practices (GCP) governing SOPs (standard operating procedures) and clinical study protocols. This includes responsibility for research assessment and patient intervention under the supervision of the Principal Investigator. Responsible for regulatory coordination of clinical research studies preparation submission and maintenance of regulatory files to fulfill research requirements. Additional responsibilities include regulatory compliance patient recruitment and enrollment data collection research chart documentation quality assurance report preparation and protocol information dissemination to healthcare professionals patients and their family members. Work may be assigned by Senior Management and assignments may be changed on an asneeded basis in order to ensure that studies and patient care needs are handled appropriately and in a timely manner. Travel to other locations may be required.

Qualifications

• A multitasked individual with a minimum 2 years of experience in a clinical research coordinator role.
• College degree in medicine science health or equivalent.
• Performs management of research activities to ensure the collection of accurate clinical data within given timeline.
• Knowledge of ICG GCP guidelines and expertise to review evaluate medical data and all applicable local laws and regulations.
• Demonstrated knowledge of all components of the research process as it pertains to clinical trials and studies i.e. IRB procedures and processes data management etc
• Experience in selection and management of vendors/CROs (Central Lab IVRS EDC)
• Track progress of clinical studies with regard to budget study milestones and deadlines.
• Recruiting & enrolment of patients who meet eligibility criteria scheduling completing CRFs.
• Able to solve complex problems prioritize multiple tasks plan proactively and accomplish goals within project in a dynamic team environment
• Participate in study audits as applicable