Jobs · Analyst · Indiana

Clinical Research Coordinator II - VANGUARD (TAMC)

On-siteAnalyst$61k–$75k/yrFull-time

Responsibilities

  • Screens patients for eligibility in participation of research protocol(s).
  • Reviews patient medical records; assists with participant identification, recruitment and enrollment.
  • Obtains informed consent and provides education about the research study, roles, and other vital information.
  • Interviews participants regarding medical history and collects questionnaire data based on self-report and medical record review.
  • Collections, processes and ships blood specimens according to established procedures.
  • Responsible for strict adherence to SOPs, research protocols and policies for all assigned research projects.
  • Aids in regulatory submissions and actions as needed.
  • Performs data entry for research projects ensuring that data is entered for analysis in a timely, efficient, and accurate manner.
  • Maintains confidentiality and security of data.
  • Maintains laboratory standards and inventories in accordance with good laboratory practices.
  • Interfaces with various clinic providers and administrative personnel.
  • Adheres to legal, professional, and ethical codes with respect to confidentiality and privacy.
  • Affirms that protocol requirements are achieved within good clinical practices.
  • Aids in monitoring audits/visits for protocols.
  • Participates in routine (weekly/monthly) update calls with MCC and site PI.
  • Oversees the maintenance of supplies, procurement, and shipping of study-related materials.

Qualifications

  • Bachelor's Degree, preferably in Life Science and/or Chemistry.
  • Minimum of 3-5 years experience required.
  • 3 years experience working in a clinical setting.

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