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

  • Interest in and knowledge of specific study indications
  • Excellent computer skills
  • Advanced knowledge of electronic equipment (i.e., e-mail, computer, fax machine, copier, etc)
  • Skill in organization and record maintenance
  • Skill in developing and maintaining effective working relationships with supervisors and co-workers
  • Strong personal initiative
  • 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 clearly communicate both orally and verbally

Duties

DUTIES INCLUDE, BUT ARE NOT LIMITED TO:

  • Creating and maintaining screen books and patient charts for all assigned studies
  • Preparing participant visits based on CRCs schedule, ensuring all source documents, assessments, lab kits and other visit materials are available and accurate. Filing of lab results, EKG results, and other communication in designated patient charts
  • Maintaining inventory of study specific supplies including lab kits, assessments and participant facing materials
  • Timely completion of data entry and query resolution for all CRFs, based on sponsor specific timelines and deadlines established in contract or other communication
  • Assisting Coordinators in assessments, including but not limited to, blood pressure, urine collection
  • Communicating with study participants, caregivers, third party vendors and laboratories as needed
  • 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
  • Other duties as assigned

Qualifications

  • BA/BS preferred
  • One (1) year experience in clinical research preferred but not required
Apply for this job

ACMR uses cookies to collect information on how visitors behave on our website. The information we collect will not be linked with a visitor's identity.
By continuing to use our website, you agree to our use of cookies.