Supv Clinical Research

Baylor Scott & White Health•Dallas, TX

About The Position

The Clinical Research Supervisor oversees the daily supervision of Clinical Research staff. The role develops, negotiates, and monitors budgets for funded research projects, facilitates implementation of clinical research projects, and ensures their quality and timely completion. The supervisor supports clinical trials and regulatory submissions, coordinates staff training and project assignments, and helps establish the financial and clinical feasibility of research.

Requirements

  • Bachelor's degree or four years of work experience above the minimum qualification.
  • Two years of experience.
  • Basic Life Support (BLS), per department requirements.
  • Proven written and oral communication skills.
  • Proven computer skills, including Microsoft Office, Excel, and PowerPoint.
  • Ability to manage time-sensitive projects and meet deadlines.
  • Ability to establish and maintain effective working relationships.
  • Excellent leadership skills.

Nice To Haves

  • Research certification or other certifications per specialty area preferred.

Responsibilities

  • Writes and assists in developing departmental proposals, grants, contracts, and budgets.
  • Assists in developing new protocols and materials from study sponsors, and provides input to Principal Investigators and management on clinical and research issues to establish financial and clinical feasibility.
  • Assists various Principal Investigators, through delegated authority, in conducting clinical trials in accordance with federal, state, and institutional guidelines.
  • Prepares initial project submissions, amendment notifications, SAE reports, continuing review reports, and other IRB reports; reviews staff-prepared submissions to ensure they meet established standards.
  • Oversees staff completion of case report forms for all studies and assists in coordinating audits by study sponsor monitors.
  • Monitors assigned Clinical Research funds.
  • Orients, trains, supervises, and evaluates Clinical Research staff; encourages growth through complex responsibilities and education programs; and coordinates project assignments.
  • Establishes and maintains good relations with the public, patients, and staff, and promotes the department's research programs.
  • Monitors communication with the IRB, FDA, and other applicable regulatory agencies.

Benefits

  • Immediate eligibility for health and welfare benefits
  • 401(k) savings plan with dollar-for-dollar match up to 5%
  • Tuition reimbursement
  • PTO accrual beginning Day 1
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