Full-Time

Clinical Trials Manager

School of Medicine, Emergency Medicine

Deadline 3/4/27
Emory University

Emory University

No salary listed

Atlanta, GA, USA

In Person

In-person at Emory; occasional remote days may be granted at department discretion.

Category
Medical, Clinical & Veterinary (1)
Required Skills
Ruby
Google Cloud Platform
Requirements
  • A bachelor's degree in a related field and seven (7) years experience in clinical trials, two of which are in the clinical area.
  • A master's degree and four years of experience in clinical trials, one of which is in the clinical area will be considered equivalent.
Responsibilities
  • Manages the financial, regulatory, patient management, and human resources functions associated with conducting clinical trials.
  • Typically supervises a staff of 2 - 5 employees.
  • Trains new clinical trials staff.
  • Tracks enrollment, sponsor payments, and salary.
  • Provides leadership in business development.
  • Assists residents in preparing research projects by facilitating IRB submissions and protocol writing.
  • Responsible for preparing NIH proposals and routing through the system.
  • Assists in creating and maintaining Standard Operating Procedures.
  • Performs related responsibilities as required.
  • Provides leadership and oversight of significant clinical research project(s) with an emphasis on managing, evaluating and training research staff.
  • Recruits, orients, and typically manages a research and administrative staff of eight to fifteen employees.
  • Plans protocol, develops policies and establishes standards for the research unit.
  • Develops and writes proposals for grants to conduct research.
  • Manages research studies and related protocols.
  • Acts as a resource person for the medical staff and community outreach.
  • Develops and provides educational information and expertise in research protocol and research driven treatment modalities.
  • Collaborates with others to develop and oversee effective internal quality assurance and control procedures.
  • Demonstrates a knowledge of and competency in all regulatory requirements (FDA, GCP, ICH and HIC).
Desired Qualifications
  • Six years clinical trials research experience which includes previous project management or leadership experience.
  • Two years of supervisory or managerial experience.
  • Certified Research Administrator (CRA) or Clinical Research Coordinator (CRC).
  • Previous grant writing experience. Knowledgeable and proficient in the use of various computer applications/systems.
  • May be required to work with, take specific precautions against and/or be immunized against potentially hazardous agents.

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