Full-Time

Clinical Trials Manager

School of Medicine, Pediatrics

Posted on 9/13/2025

Deadline 11/4/26
Emory University

Emory University

No salary listed

Atlanta, GA, USA

Hybrid

In-person at Emory location; remote work from home days may be granted at department discretion.

Category
Medical, Clinical & Veterinary (3)
, ,
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.
  • In collaboration with principal investigator(s), oversee the implementation and supervision of multi-site clinical trials and surveillance funded by federal and industry sponsors.
  • Manage the contractual funding process with the sponsors and Emory financial team.
  • Coordinate with regulatory and clinical research teams at participating sites to facilitate effective study start-up, enrollment, and retention as outlined by study protocols.
  • Serve as a leadership hub, providing guidance to study teams across multiple sites.
  • Manage communications with stakeholders and assess progress toward study goals throughout the contractual period.
  • Collaborate with local site teams to assess personnel needs and provide supervision and support as required.
  • Develop clinical trial protocols and summary reports.
  • Lead internal projects as needed.
Desired Qualifications
  • 5–7 years of experience in clinical trial management, preferably in diverse roles across different studies.
  • Proven program management experience, particularly in multi-site, multi-department, or multi-organization collaborations.
  • Strong knowledge of clinical trial regulations, sponsor requirements, and compliance standards.
  • Experience in budgeting, financial oversight, and grant proposal preparation.
  • Postgraduate education demonstrating the ability to plan, organize, and execute research projects.
  • Excellent leadership, communication, and organizational skills.

Company Size

N/A

Company Stage

N/A

Total Funding

N/A

Headquarters

N/A

Founded

N/A

INACTIVE