Start Date
Immediate
Expiry Date
16 Nov, 25
Salary
33.1
Posted On
16 Aug, 25
Experience
3 year(s) or above
Remote Job
Yes
Telecommute
Yes
Sponsor Visa
No
Skills
Spreadsheets, Confidentiality, Medical Terminology, Databases, Communication Skills, Medical Records
Industry
Pharmaceuticals
POSITION SUMMARY
This position is responsible for handling key functions for research studies, such as participant consenting, screening, enrollment, registrations, and compiling and submitting data related to participants engaged in applicable research studies. Monitors study compliance and maintains a system for effective data flow associated with research protocols.
MINIMUM QUALIFICATIONS
Possession of basic knowledge as normally obtained by the completion of an Associate’s degree.
Knowledge of basic laboratory procedures as normally obtained through the completion of three to five years experience in a health care setting, preferably in a research environment. Extensive knowledge and understanding of medical terminology in order to read, identify, and extract pertinent data from medical records and information. Ability to multi-task and re-prioritize duties as needed. Ability to maintain confidentiality. Excellent human relations, organizational and communication skills.
Must be knowledgeable of data entry and computer programs associated with maintaining databases, spreadsheets, etc.
PREFERRED QUALIFICATIONS
Prior experience in phlebotomy and laboratory specimen processing. Bachelor’s Degree and/or Certified Research Certification
Additional related education and/or experience preferred.
Please refer the Job description for details