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Clinical Research Associate - Data Entry


Precision Clinical Research
Headquarters: Lauderdale Lakes, FL
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Clinical Research Associates are responsible for collecting information about patients’ medical histories and clinical trials. Associates will work with computerized patient records and clinical trial data to ensure it is precisely sorted and recorded within the CTMS. In addition to inputting data, associates may be asked to perform a number of duties including but not limited to marketing (social media posts, creation of flyers, etc.), filing, light accounting, assisting coordinators and other team members.
Clinical Research Associate – Data Entry must have:
  • Experience in clinical research trials and medical knowledge of multiple conditions
  • General Knowledge of HIPAA compliance and Federal Regulations on human Subjects Research and Good Clinical Practice guidelines
  • Ability to comprehend clinical research protocols
  • Effective communication skills (written and verbal) with good customer service skills
  • Familiar with Social Media and other marketing / advertising methods
  • Proven ability to meet timelines and manage work independently
  • Proficient in Microsoft Office Suite (Word, Excel, Outlook) and CTMS such as Clinical Conductor
  • Detail oriented with superior organization and documentation skills
  • Proven ability to work unilaterally or within diverse teams
  • Ability to establish and maintain successful relationships with a variety of people
  • Bilingual a plus
Job Type: Full-time or Part-time
Required Experience: Research – 2 Years
Required Education: GED or equivalent

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