Clinical Research Coordinator

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profile Job Location:

Fairfield, OH - USA

profile Monthly Salary: Not Disclosed
Posted on: Yesterday
Vacancies: 1 Vacancy

Job Summary

Job Description

Contact: Alexandra Spink -
No 3rd party candidates


Clinical Research Coordinator

The Clinical Research Coordinator is responsible for supporting and overseeing the successful execution of clinical trials while ensuring compliance with regulatory and ethical standards. This role manages research operations data integrity participant engagement and coordination with internal and external stakeholders.

Key responsibilities include:

  • Oversee the smooth and efficient operation of clinical trials
  • Collect code and analyze data obtained from research activities
  • Manage research budgets and track study-related expenditures
  • Inform research participants of study objectives procedures and expectations
  • Administer questionnaires and other research instruments
  • Monitor research participants to ensure adherence to study protocols and rules
  • Ensure compliance with all applicable research regulatory standards
  • Adhere to established ethical guidelines throughout all phases of research
  • Maintain detailed and accurate study records in accordance with FDA guidelines including drug dispensation documentation
  • Liaise with laboratories regarding test results and research findings
  • Participate in subject recruitment initiatives and enrollment efforts
  • Ensure all required study supplies and equipment are available maintained and in proper working order
  • Engage with research subjects to address questions concerns and overall study experience
  • Collaborate with internal teams and external partners to support study success

Required Skills and Qualifications

  • Associates degree in Nursing or a science-related field
  • Minimum of two (2) years of experience in healthcare clinical research management or data collection
  • Strong analytical mindset with attention to detail
  • Proven problem-solving abilities
  • Experience writing technical or scientific papers
  • Exceptional interpersonal skills with the ability to engage effectively with participants and team members
  • Outstanding written and verbal communication skills
  • Excellent organizational and time management skills
  • Willingness and ability to continually self-educate and stay current with research practices
  • Some experience managing or supporting other team members and interns

Required Experience:

IC

Job Description Contact: Alexandra Spink - No 3rd party candidatesClinical Research CoordinatorThe Clinical Research Coordinator is responsible for supporting and overseeing the successful execution of clinical trials while ensuring compliance with regulatory and e...
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