Site CRC 1 - OK - QTLSJP00005849 in Oklahoma City, OK at Apex Life Sciences

Date Posted: 1/29/2018

Job Snapshot

  • Employee Type:
    Full-Time
  • Job Type:
    Other
  • Experience:
    At least 1 year(s)
  • Date Posted:
    1/29/2018
  • Job ID:
    817512

Job Description


PURPOSE:

  • To work as an integral member of partner/investigator site staff maintaining the day-to-day relationship with a partner site/s involving planning, coordinating and, as appropriate, execution of clinical studies in accordance with the protocol, contracted scope of work, ICH/GCP, Sponsor/IQVIA SOP's and any relevant local guidelines and regulations.

RESPONSIBILITIES:

  • Work directly at patient/subject interface at investigator sites to deliver high quality patient data in accordance with local regulations, agreed scope of work and as required by protocol.
  • Assist with screening and enrollment of subjects into an in depth Schizophrenia clinical trial.
  • Support subjects on trials to encourage maximum retention and future recruitment.
  • Assist with the establishment of a recruitment and contingency plan for each study.
  • Perform functions necessary for successful completion of all protocol required visits/procedures such as vital signs, phlebotomy, diagnostic tests, dispensing of investigational product, scheduling, drug accountability/reconciliation and organizational tasks, where appropriate and as delegated by the investigator, in accordance with local country requirements.
  • Accurately complete source documents and case report forms in both paper and electronic format.
  • Assist investigator with recording and reporting of adverse events as per local regulatory authority guidelines.
  • Perform other duties as assigned per protocol, IQVIA and / or investigator.

REQUIRED KNOWLEDGE, SKILLS AND ABILITIES:

  • Good knowledge of medical terminology.
  • Above average interpersonal and organizational skills.
  • Proficient in the use of Microsoft Office.
  • Fluent in local language, spoken and written.
  • Fluent in written English language.
  • Ability to work independently, prioritize actively, seek input, problem solve and work in a team environment.
  • Ability to maintain confidentiality.
  • Ability to establish and maintain effective working relationships with coworkers, managers and clients.

MINIMUM REQUIRED EDUCATION AND EXPERIENCE:

  • Registered nurse, medical physician or appropriate educational qualification and minimum 1 years' experience being a Clinical Research Coordinator.
  • Experience in Schizophrenia or Psychology based clinical studies is a strong preference.

EEO Employer

Apex is an Equal Employment Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, age, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other characteristic protected by law. Apex will consider qualified applicants with criminal histories in a manner consistent with the requirements of applicable law. If you have visited our website in search of information on employment opportunities or to apply for a position, and you require an accommodation in using our website for a search or application, please contact our Employee Services Department at employeeservices@apexsystemsinc.com or 844-463-6178.