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Clinical Research Coordinator

Medix™

This is a Full-Time position in Nashville, TN posted January 24, 2023.

We’re looking for career minded, team players who want to grow along with us and create an excellent patient experience for those enrolled in our clinical trials in Nashville, TN! We are open to those looking to relocate to Tennessee. If you’re a Clinical Research professional ready to take the next step in their career and live in the Music City! This onsite Coordinator will work in oncology trials in a fast paced environment.

HIRING IMMEDIATELY – CANCER TRIALS – 401K

GREAT PAY – TUITION ASSISTANCE – BENEFITS –GROWTH

Key Responsibilities:

  • Prepares, processes and manages new research proposals, amendments, continuing review applications, adverse event reports, budgets, and D&H accounts
  • Prepares and maintains documents required to be maintained internally and available for regulatory authorities and/or the sponsor prior to, during and after the conduct of a clinical trial
  • Participates in periodic site visits from sponsor, regulatory authorities and others to review research, source documentation and research procedures
  • Participates in data quality assurance reviews
  • Participates in the determination of eligibility and recruits candidates for study participation
  • Records data from source documentation and/or participant interaction onto case report forms (either paper or electronic) with awareness and attention to the requirements for accuracy, completeness and timeliness
  • Monitors, detects and reports adverse events meeting requirements of regulatory bodies
  • Performs packaging and ships study specimens (blood, urine, etc.) to the sponsor or laboratory in accordance with sponsor and shipping guidelines and regulations, maintaining appropriate documentation
  • Responsible for study completion processes including study closeout, reporting and archiving of study files, ensuring completeness and continuity of all study data, performing ongoing checks of clinical data that has been entered on the case report forms (paper or electronic) or in reports and assuring archival of appropriate/required documentation
  • Participates in the ongoing screening and informed consent process
  • Develops recruitment and retention strategies to improve study performance

Must Have:

  • Minimum 3 years of clinical research experience
  • Bachelor’s degree preferred
  • Full time, In-person: Monday- Friday 8am- 5pm (some flex hours)

Benefits

  • Full benefits: medical, dental, vision insurance
  • 401k with employer match
  • 14 days of PTO plus paid federal holidays
  • Tuition Assistance, Adoption Assistance, and FSA and more!

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