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Posted: Tuesday, February 6, 2018 9:00 PM

Clinical Research Coordinator (CRC) I, Los Angeles, CA

As a Clinical Research Coordinator (CRC I), you will work with patients to screen / assess patient eligibility for the clinical study. This position will involve working between our Clinical Research Support (CRS) and hospital site, both of which are on our campus.

Summary: The Clinical and Translational Science Institute (CTSI) is establishing a centralized Clinical Research Support (CRS) Office for research teams conducting non-cancer clinical studies. The CRS Clinical Research Coordinator will join a team of coordinators, serving clinical researchers across our campus. This role will have the opportunity to work on studies of varying disease types and provide a range of study-related services, ranging from regulatory document preparation, participant recruitment, data collection, and study monitoring. Assist investigators or other staff with aspects of sponsor initiated and investigator-initiated research studies.

Key Responsibilities:
  • Assists with organizing and scheduling assessments/tests/activities to meet research objectives and study protocol compliance. Communicates with study team personnel to ensure study procedures are followed and research is performed as described in protocol. Serves as contact for subjects, study personnel, Institutional Review Board (IRB) and study sponsor.
  • Participates in assessing patient eligibility. Assists in coordinating study participant activities including recruitment, screening, orientation and correspondence. Schedules subject appointments, tests, and procedures coordinating with external providers as needed. Produces reports and other materials, as directed.
  • Assists with data collection for research studies following established data collection and management procedures. Collects, records, enters and prepares data for analysis. Performs preliminary study analysis under the direction of the Principal Investigator or senior coordinators. Collects pertinent information from study participants through interviews, administration of tests or surveys or questionnaires, medical records review, or other collection procedures.
  • Maintains accurate, complete and timely records, including source documents, consent forms, case report forms, protocol documents, and regulatory documents, as required by sponsor and institutional guidelines.
  • Assists in organization and preparation of grant proposals. Gathers documentation such as annual reports and detailed budgets for inclusion in proposal. Assists investigators in developing research proposals. Interfaces with funding and regulatory agencies to exchange information.
  • Assists with submission of timely, accurate, and complete study continuing review, amendments, and reportable events to IRB.
  • Ensures consent process is performed and documented in compliance with FDA, GCP, IRB, HIPAA, SOPs, sponsor and institutional regulations and policies.
  • Provides ongoing education to study subjects about clinical trials and provides significant new information that may affect a subjects willingness to participate in a study, when needed. Evaluates subject compliance and promotes compliance through education.
  • Assists in the preparation of site for monitor visit and external/internal audits. Provides timely response to queries from sponsor and/or auditors.
  • Collaborates with pharmacist or materials management personnel to maintain accurate accountability of investigational products and specimens.
  • Assists with sample collection, processing and shipment for each study.
  • Updates automated databases and other records for reporting and compliance purposes. Generates reports and analysis of data according to project schedules or on an ad hoc basis.
  • Assists by arranging and attending meetings, seminars, symposia and other events related to project efforts. Participates in educational opportunities to increase knowledge about clinical trials and regulations. Remains current with federal, state, and institutional regulations and best practices.
  • Orders supplies and equipment. Researches and develops recommendations for new equipment purchases.
  • Completes Research Order Form (ROF) for each subject visit and submits subject enrollment documentation as required
  • Performs other related duties as assigned or requested. The university reserves the right to add or change duties at any time.

Job Requirements:
  • Bachelor's degree. Combined experience/education as substitute for minimum education
  • 1 year of relevant experience as a CRC
  • Certified Clinical Research Coordinator.
  • Knowledge and understanding of federal, state, and institutional research regulations as well as Good Clinical Practices (GCP) and HIPPA regulations.
  • Proficient with MS Office applications. Demonstrated effective communication and writing skills.
  • Knowledge of medical environment and terminology.
  • Ability to multi-task.
  • Demonstrated ability to work as part of a team as well as independently.
  • Experience in an Academic Setting is a plus.
  • Bilingual, English / Spanish-speaking

For immediate consideration or questions, please contact Shardae at 714-###-#### now!

Why Kelly ?

With Kelly, you'll have access to some of the world's highest-regarded scientific organizations-providing you with opportunities to work on today's most challenging, research-intensive, and relevant projects. Our connections can lead you to innovative scientific pursuits you'll be proud to help advance. We work with 95 of the Fortune 100 companies, and found opportunities for more than 11,000 scientific professionals last year.
You pursued a career in science to fuel your quest for knowledge and your desire to make the world a better place. Let Kelly fuel your career-connect with us today.

About Kelly Services

As a workforce advocate for over 70 years, we are proud to directly employ nearly 500,000 people around the world and have a role in connecting thousands more with work through our global network of talent suppliers and partners. Revenue in 2016 was $5.3 billion. Visit kellyservices.com and connect with us on Facebook , LinkedIn and Twitter .
Kelly Services is an equal opportunity employer including, but not limited to, Minorities, Females, Individuals with Disabilities, Protected Veterans, Sexual Orientation, Gender Identity and is committed to employing a diverse workforce. Equal Employment Opportunity is The Law.

Kelly complies with the requirements of the Fair Chance Initiative. A conviction record does not automatically bar individuals from employment.


Associated topics: clinical, clinical development, clinical informatics, clinical trial, coordinator, lab, laboratory, research, research coordinator

Source: http://www.jobs2careers.com/click.php?id=4811490583.96


• Location: Los Angeles

• Post ID: 160687777 losangeles
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