Senior Clinical Research Coordinator

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  • Full Time
  • Anywhere

Job Description


An individual who, under the direction and ongoing supervision of the Principal Investigator, aids in the daily function of clinical research programs being performed by Hope Clinical Research.


  • Responsibilities may include, but are not limited to the following:
  • Communicates effectively and courteously with study patients
  • Demonstrates a caring attitude toward patients and their families
  • Acknowledges study patients’ needs and tends to them appropriately
  • Collects patient medical history and conditions
  • Obtain Informed Consent
  • Study drug dispense and accountability
  • Collect and evaluate concomitant medication
  • Collect and evaluate medical records for compliance
  • Conduct A/E and SAE assessments
  • Perform EKG, vital signs and protocol specific procedures
  • Collect and process blood, urine and tissue samples
  • Evaluate clinical blood lab reports
  • Maintains office site regulatory files
  • Verify accuracy of data collected
  • Document temperatures for IP stored on-site
  • Recruit study patients by calling subjects from database
  • Participate in offsite recruitment events as directed by Hope Clinical
  • Developing study e-source documents to comply with study protocol
  • Manage all required study startup documentation, training, and timelines on assigned study protocols
  • Assist in staff/office management
  • Train new staff
  • Other tasks and responsibilities as requested by Hope Clinical to facilitate business needs

QUALIFICATIONS AND SKILLS (May include, but are not limited to):

  • Comprehensive knowledge of FDA, GCP and HIPAA as applied to clinical research
  • Knowledge of current studies being conducted
  • Comprehensive knowledge of company’s SOPs, policies and Confidentiality agreements
  • Knowledge of safety hazards and procedures that establish a safe work environment
  • Skilled in computer and data collection software
  • Phlebotomy, EKG, and other technical skills as required per protocol.

CERTIFICATES, LICENSES, REGISTRATION (May include, but are not limited to):

  • Accredited medical degree and/or certification program and/or two years research experience
  • CPR and first aid certification
  • IATA and/or Safe-T-Pak certification for shipment lab specimens and/or dry ice
  • GCP and protection of Human Subject Participants


  • Strong written and verbal skills
  • Proficient with Microsoft Office, Visio, and Project


  • Certified Medical Assistant and/or phlebotomy
  • Microsoft SharePoint experience
  • Prior knowledge of medical terminology
  • Ability to operate with limited direction
  • Good customer service skills
  • Conflict resolution
  • Problem solver
  • Quick learner
  • Multi-task
  • Management skill

Job Type: Full-time

Salary: $18.00 to $25.00 /hour plus bonus, health insurance and paid time off/vacations

Job Type: Full-time

Salary: $18.00 to $25.00 /hour


  • Clinical Research Coordinator: 3 years (Required)
  • Clinical Research: 3 years (Required)


  • Medical Assistant or Phlebotomist (Preferred)


Work authorization:


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