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Clinical Research Manager (68740)
Job Location:
Job Location:
Atlanta, GA - USA
Monthly Salary:
Not provided by the employer
Monthly Salary:
Posted:
13 August 2026 (30+ days ago)
Posted:
Application Deadline:
10 November 2026
Application Deadline:
Vacancies:
1 Vacancy
Vacancies:
Job Summary
Description
GENERAL SUMMARY OF DUTIES:Leads day-to-day multi-site clinical research operations staff and study execution from feasibility through closeout in alignment with the Directors strategy.
Exceptional candidates with experience beyond the posted level are encouraged to apply. Based on qualifications experience and organizational needs consideration may be given to placement at a higher level.
RESPONSIBILITIES:
Duties include but are not limited to:
Duties include but are not limited to:
- Supervise and provide leadership to Clinical Research Coordinators and Research Assistants/Interns
- Lead day-to-day multi-site clinical research operations and promote consistent efficient study execution
- Manage the study lifecycle from feasibility and startup through conduct monitoring and closeout
- Track enrollment timelines milestones compliance and data quality; resolve issues and escalate significant risks
- Serve as the operational liaison among investigators sponsors CROs vendors staff and centralized support teams
- Ensure regulatory documentation and study activities meet FDA ICH-GCP HIPAA IRB sponsor and organizational requirements
- Conduct quality reviews implement SOPs and CAPAs and maintain audit and inspection readiness
- Recruit onboard train mentor evaluate and allocate research staff based on study and site priorities
- Support research systems standardized workflows and practical process improvements across sites
EDUCATION SKILLS & EXPERIENCE:
- Required:
- Bachelors degree in nursing life sciences public health healthcare administration or a related field
- At least five years of clinical research experience including study coordination or site management and direct supervision of research personnel.
- Demonstrated experience managing study startup site activation conduct monitoring closeout and multi-site operational workflows
- Knowledge of FDA regulations ICH-GCP HIPAA and IRB requirements with strong project management people-leadership communication and organizational skills
- Preferred:
- Masters degree in clinical research healthcare administration public health nursing or a related field
- Clinical research certification and experience with research systems and process improvement
WORK ENVIRONMENT:
Requires sitting and standing associated with a normal office environment. Travel required as business needs dictate.
Requires sitting and standing associated with a normal office environment. Travel required as business needs dictate.
DRUG FREE WORKPLACE:
United Digestive is a drug-free workplace. All offers of employment are contingent upon passing a pre-employment drug screening.
United Digestive is a drug-free workplace. All offers of employment are contingent upon passing a pre-employment drug screening.
EQUAL OPPORTUNITY EMPLOYER:
United Digestive is an equal opportunity employer and will not tolerate discrimination in employment on the basis of race color age sex sexual orientation gender identity or expression religion disability ethnicity national origin marital status veteran status genetic information or any other legally protected classification or status.
United Digestive is an equal opportunity employer and will not tolerate discrimination in employment on the basis of race color age sex sexual orientation gender identity or expression religion disability ethnicity national origin marital status veteran status genetic information or any other legally protected classification or status.
IND123
Required Experience:
Manager
