Atlanta Center for Medical Research

Scope

GENERAL SUMMARY OF DUTIES

Provides direct support to Clinical Research Coordinators in the completion of protocol-specific study goals while observing strict adherence to ICH, GCP, protocol, and ACMR guidelines, regulations, and policies.

KNOWLEDGE, SKILLS & ABILITIES

  • Knowledge of electronic equipment (i.e, e-mail, computer, fax machine, copier, etc)
  • Knowledge of medical equipment and instruments to administer study subject care
  • Skill in organization and record maintenance
  • Skill in developing and maintaining effective working relationships with supervisors and co-workers
  • Ability to complete paperwork with precision and attention to detail
  • Ability to react calmly and effectively in emergency situations
  • Ability to interpret, adapt and apply guidelines and procedures
  • Ability to work independently as well as functioning as part of a team
  • Ability to clearly communicate both orally and verbally

Duties

DUTIES INCLUDE, BUT ARE NOT LIMITED TO:

  • Creating and maintaining screen books and charts for all assigned studies
  • Preparing visits for the next day, ensuring accuracy of source documents and assessments
  • Filing of lab results, EKG results, and other communication in designated charts
  • Timely completion of data entry for all eCRFs, as well as paper CRF completion and transmission
  • Completion of headers
  • Assisting Coordinators in assessments, including but not limited to, blood pressure and urine drug screens
  • Assisting Coordinators with scheduling, copying, faxing, and other clerical tasks
  • Aiding Coordinators in the facilitation of study monitoring visits
  • Completion of daily responsibilities delegated by CRC as they pertain to the study and/or participants

Qualifications

  • BA/BS in science disciplines is mandatory
  • One (1) year experience in clinical research preferred
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