
Clinical Trials Manager | School of Medicine - Pediatrics
- Atlanta, GA
- Permanent
- Full-time
- 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.
- 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.
- 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.