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Clinical Research Coordinator Sr FSM/CC

at Northwestern University in Evanston, Illinois, United States

Job Description

Job Opening Id: 50448

Department: MED-Cancer Center
Salary/Grade: EXS/8
 

Job Summary: 

Manages all activities associated with biomedical &/or social-behavioral research studies considered very complex by the inclusion of several of the following: multiple investigators, teams, sites, sub-contracts, participants, longitudinal assessments/ interventions; &/or multi-million dollar budgets. Ensures completion of contract requirements & client specifications. Oversees day-to-day operations including identifying & securing needed resources. Creates, implement, monitors & updates project plans. Facilitates meetings with appropriate parties. Tracks tasks/deliverables to ensure timelines, milestones &/or goals are attained. Monitors & reports progress as appropriate. Resolves &/or escalates issues in a timely manner. Co-authors scientific papers for presentation & publication & coordinates writing, submission & administration of grants. Ensures that all study activities are completed by strictly following Good Clinical Practices (GCP) & all current local, state, & federal laws, regulations, guidance, policy & procedure developed by the NU Institutional Review Board (IRB), Food & Drug Administration (FDA) Code of Federal Regulations (CFR), & the International Conference on Harmonization (ICH). Please note: Supervisor provides objectives and deadlines. Work is reviewed for fulfillment of objective and deadlines and overall compliance with policy and procedures. EE completes some activities without direction, informing supervisor only of potentially controversial matters, and/or far-reaching implications.

 

Specific Responsibilities:

Technical

  • Provides complex scientific & technical leadership in determining research priorities & the plan, design & execution of research projects ensuring that programs of investigation meet specified objectives. 
  • Plans, develops & implements new processes & protocols to support research studies & maximize/extend study capabilities. 
  • Oversees completion of study activities per protocol. Collaborating with nursing staff and Principal Investigator (PI) ascertains pretreatment & eligibility requirements; interviews participants & obtains social & medical histories; based on results determines & registers participants with appropriate sponsors; completes informed consent; determines & organizes patient's treatment and test schedules. 
  • Ensures that study protocols are in compliance with appropriate rules & r
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Job Posting: 11968870

Posted On: Jun 11, 2024

Updated On: Jul 10, 2024

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