About the role

  • Clinical Research Coordinator providing assistance on clinical research studies including recruiting and organizing data. Supporting patient consent and clinical tests within a hybrid work setting.

Responsibilities

  • Provides assistance on clinical research studies, including recruiting, evaluating, and consenting patients for studies
  • Collecting and organizing patient data
  • Scheduling patients for study visits
  • Performing clinical tests such as phlebotomy, EKGs, etc.
  • Maintaining and updating data generated by the study
  • Reviewing proposals for compliance with sponsor and organizational guidelines
  • Verifying that all sponsor requirements are met
  • Conducting phone interviews to recruit patients for clinical trials
  • Verifying the accuracy of study forms and updating them per protocol
  • Preparing data for analysis and data entry
  • Documenting patient visits and procedures
  • Assisting with regulatory binders and QA/QC Procedures
  • Assisting with interviewing study subjects
  • Assisting with study regulator submissions

Requirements

  • Bachelor's Degree Related Field of Study required
  • Some relevant research project work 0-1 year preferred
  • Careful attention to detail and good organizational skills
  • Ability to follow directions
  • Good interpersonal and communication skills
  • Computer literacy
  • Working knowledge of clinical research protocols.

Benefits

  • competitive base pay
  • comprehensive benefits
  • career advancement opportunities
  • differentials
  • premiums
  • bonuses as applicable
  • recognition programs designed to celebrate your contributions and support your professional growth

Job title

Clinical Research Coordinator I

Job type

Experience level

Junior

Salary

$20 - $28 per hour

Degree requirement

Bachelor's Degree

Location requirements

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