Manages the financial, regulatory, patient management, and human resources functions associated with conducting clinical trials. * Typically supervises a staff of 2 - 5 employees/students.
Manages the financial, regulatory, patient management, and human resources functions associated with conducting clinical trials. * Typically supervises a staff of 2 - 5 employees/students.
Manages the financial, regulatory, patient management, and human resources functions associated with conducting clinical trials. * Typically supervises a staff of 2 - 5 employees/students.
Manages the financial, regulatory, patient management, and human resources functions associated with conducting clinical trials. * Typically supervises a staff of 2 - 5 employees/students.
Manages the financial, regulatory, patient management, and human resources functions associated with conducting clinical trials. * Typically supervises a staff of 2 - 5 employees/students.
Manages the financial, regulatory, patient management, and human resources functions associated with conducting clinical trials. * Typically supervises a staff of 2 - 5 employees/students.
We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers ... What the Project Management department does at Worldwide Worldwide Clinical Trials Project ...
We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers ... What the Project Management department does at Worldwide Worldwide Clinical Trials Project ...
Litigation Associate
Atlanta, GA · On-site
Participate in depositions, hearings, mediations, and trials * Manage cases focused on product liability, premises liability, general liability, and automobile/trucking litigation Qualifications:
Litigation Associate
Atlanta, GA · On-site
Participate in depositions, hearings, mediations, and trials * Manage cases focused on product liability, premises liability, general liability, and automobile/trucking litigation Qualifications:
Manages post-award activities for an assigned portfolio of clinical trials within a Research Administration Services (RAS) unit using knowledge of grant, contract, and clinical trial management rules ...
Manages post-award activities for an assigned portfolio of clinical trials within a Research Administration Services (RAS) unit using knowledge of grant, contract, and clinical trial management rules ...
Manages post-award activities for an assigned portfolio of clinical trials within a Research Administration Services (RAS) unit using knowledge of grant, contract, and clinical trial management rules ...
Manages post-award activities for an assigned portfolio of clinical trials within a Research Administration Services (RAS) unit using knowledge of grant, contract, and clinical trial management rules ...
Manages post-award activities for an assigned portfolio of clinical trials within a Research Administration Services (RAS) unit using knowledge of grant, contract, and clinical trial management rules ...
Manages post-award activities for an assigned portfolio of clinical trials within a Research Administration Services (RAS) unit using knowledge of grant, contract, and clinical trial management rules ...
ITSS-Product Owner
Atlanta, GA · On-site
May be responsible for feasibility studies, field trials management, identifying product gaps, defining product requirements and engaging with customers to understand market needs and trends.
ITSS-Product Owner
Atlanta, GA · On-site
May be responsible for feasibility studies, field trials management, identifying product gaps, defining product requirements and engaging with customers to understand market needs and trends.
Responsibilities involve patient registration, data management, adverse event reporting, maintenance of a Clinical Trials Management System, and other activities related to research. The RDS works ...
Responsibilities involve patient registration, data management, adverse event reporting, maintenance of a Clinical Trials Management System, and other activities related to research. The RDS works ...
Clinical Trials Operations (CTO) Director - Clinical & Operational Implementation
Atlanta, GA · On-site
Financial Management & Billing Compliance (Operational Execution) • Build/manage study budgets ... Clinical Trials staff
Clinical Trials Operations (CTO) Director - Clinical & Operational Implementation
Atlanta, GA · On-site
Financial Management & Billing Compliance (Operational Execution) • Build/manage study budgets ... Clinical Trials staff
Responsibilities involve patient registration, data management, adverse event reporting, maintenance of a Clinical Trials Management System, and other activities related to research. The RDS works ...
Responsibilities involve patient registration, data management, adverse event reporting, maintenance of a Clinical Trials Management System, and other activities related to research. The RDS works ...
Responsibilities involve patient registration, data management, adverse event reporting, maintenance of a Clinical Trials Management System, and other activities related to research. The RDS works ...
Responsibilities involve patient registration, data management, adverse event reporting, maintenance of a Clinical Trials Management System, and other activities related to research. The RDS works ...
Responsibilities involve patient registration, data management, adverse event reporting, maintenance of a Clinical Trials Management System, and other activities related to research. The RDS works ...
Responsibilities involve patient registration, data management, adverse event reporting, maintenance of a Clinical Trials Management System, and other activities related to research. The RDS works ...
Responsibilities involve patient registration, data management, adverse event reporting, maintenance of a Clinical Trials Management System, and other activities related to research. The RDS works ...
Responsibilities involve patient registration, data management, adverse event reporting, maintenance of a Clinical Trials Management System, and other activities related to research. The RDS works ...
Responsibilities involve patient registration, data management, adverse event reporting, maintenance of a Clinical Trials Management System, and other activities related to research. The RDS works ...
Responsibilities involve patient registration, data management, adverse event reporting, maintenance of a Clinical Trials Management System, and other activities related to research. The RDS works ...
Responsibilities involve patient registration, data management, adverse event reporting, maintenance of a Clinical Trials Management System, and other activities related to research. The RDS works ...
Responsibilities involve patient registration, data management, adverse event reporting, maintenance of a Clinical Trials Management System, and other activities related to research. The RDS works ...
Responsibilities involve patient registration, data management, adverse event reporting, maintenance of a Clinical Trials Management System, and other activities related to research. The RDS works ...
Responsibilities involve patient registration, data management, adverse event reporting, maintenance of a Clinical Trials Management System, and other activities related to research. The RDS works ...
Responsibilities involve patient registration, data management, adverse event reporting, maintenance of a Clinical Trials Management System, and other activities related to research. The RDS works ...
Responsibilities involve patient registration, data management, adverse event reporting, maintenance of a Clinical Trials Management System, and other activities related to research. The RDS works ...
Responsibilities involve patient registration, data management, adverse event reporting, maintenance of a Clinical Trials Management System, and other activities related to research. The RDS works ...
Responsibilities involve patient registration, data management, adverse event reporting, maintenance of a Clinical Trials Management System, and other activities related to research. The RDS works ...
Trials Manager information
What are the key skills and qualifications needed to thrive as a Trials Manager, and why are they important?
To thrive as a Trials Manager, you need a solid background in clinical research, project management, and regulatory compliance, typically supported by a relevant scientific degree and experience in clinical trials. Familiarity with clinical trial management systems (CTMS), Good Clinical Practice (GCP) guidelines, and often certifications like ACRP or SOCRA are highly valuable. Strong leadership, organization, and communication skills help manage multidisciplinary teams and ensure protocol adherence. These competencies are crucial for delivering safe, efficient, and compliant clinical trials that advance medical research.
What are Trials Managers?
Trials Managers are professionals responsible for overseeing and coordinating clinical trials or research studies. They manage all aspects of the trial process, including planning, organizing, and ensuring that studies are conducted in accordance with regulatory guidelines and protocols. Their role often involves liaising with sponsors, investigators, and regulatory authorities, as well as monitoring progress and reporting results. Trials Managers play a key role in ensuring that trials are completed on time, within budget, and to the required quality standards.
What are the main challenges a Trials Manager faces when coordinating multi-site clinical trials?
As a Trials Manager, one of the primary challenges when overseeing multi-site clinical trials is ensuring consistent protocol adherence and data quality across all locations. This involves frequent communication with site staff, troubleshooting logistical issues, and monitoring regulatory compliance. Additionally, balancing timelines and resources while managing diverse teams can be demanding. Successful Trials Managers proactively address these challenges through robust planning, regular site visits, and clear documentation to keep studies on track.
What is the difference between Trials Manager vs Clinical Research Coordinator?
| Criteria | Trials Manager | Clinical Research Coordinator |
|---|---|---|
| Required Credentials | Bachelor's degree, experience in trial management, knowledge of regulations | Bachelor's degree, clinical research experience, regulatory knowledge |
| Work Environment | Oversees multiple trials, manages teams, coordinates with sponsors | Handles daily trial activities, patient interactions, data collection |
| Employer & Industry Usage | Pharmaceutical companies, CROs, biotech firms | Hospitals, clinics, research institutions |
The Trials Manager focuses on overseeing entire clinical trials, managing teams, and ensuring compliance across multiple studies. In contrast, the Clinical Research Coordinator handles the day-to-day activities at trial sites, working directly with patients and collecting data. Both roles require similar educational backgrounds and regulatory knowledge but differ in scope and responsibilities.
What are popular job titles related to Trials Manager jobs in Georgia? For Trials Manager jobs in Georgia, the most frequently searched job titles are:
What job categories do people searching Trials Manager jobs in Georgia look for? The top searched job categories for Trials Manager jobs in Georgia are:
What cities in Georgia are hiring for Trials Manager jobs? Cities in Georgia with the most Trials Manager job openings:
Full-time
Re-posted 10 days ago
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Job description
Discover Your Career at Emory University
Emory University is a leading research university that fosters excellence and attracts world-class talent to innovate today and prepare leaders for the future. We welcome candidates who can contribute to the excellence of our academic community.
DescriptionJOB DESCRIPTION
- Manages the financial, regulatory, patient management, and human resources functions associated with conducting clinical trials.
- Typically supervises a staff of 2 - 5 employees/students.
- Coordinate with cross-functional teams to ensure the smooth execution of trials.
- Supervise site selection and initiation activities.
- Manage relationships with clinical sites and investigators.
- Participates in recruitment (multiple trials) and selection of study participants by interviewing and documenting medical history to determine compliance with eligibility requirements.
- Oversee data collection, analysis, and EDC data entry, trains new clinical trials staff.
- Tracks enrollment/targets across all trials, sponsor payments, and salary.
- Provides leadership in business development.
- Responsible for preparing and routing all proposals and routing through the various Emory systems.
- Assists in creating and maintaining Standard Operating Procedures.
- Performs related responsibilities as required.
MINIMUM QUALIFICATIONS:
- A bachelor's degree in a related field and seven (7) years experience in clinical trials, two of which are in the clinical area.
- OR a master's degree and four years of experience in clinical trials, one of which is in the clinical area will be considered equivalent.
- Strong understanding of ICH-GCP guidelines, Certified Clinical Research Professional (CCRP) or equivalent (preferred).
NOTE: This role will be granted the opportunity to work from home regularly but must be able to commute to Emory University on a flexible weekly schedule based upon business needs. Schedule is based on agreed upon guidelines of department. This role requires residency in the state of GA. Emory reserves the right to change remote work status with notice to employee.
Additional DetailsEmory is an equal opportunity employer, and qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, protected veteran status or other characteristics protected by state or federal law. Emory University does not discriminate in admissions, educational programs, or employment, including recruitment, hiring, promotions, transfers, discipline, terminations, wage and salary administration, benefits, and training. Students, faculty, and staff are assured of participation in university programs and in the use of facilities without such discrimination. Emory University complies with Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veteran's Readjustment Assistance Act, and applicable executive orders, federal and state regulations regarding nondiscrimination, equal opportunity, and affirmative action (for protected veterans and individuals with disabilities). Inquiries regarding this policy should be directed to the Emory University Department of Equity and Civil Rights Compliance, 201 Dowman Drive, Administration Building, Atlanta, GA 30322. Telephone: 404-727-9867 (V) | 404-712-2049 (TDD).
Emory University is committed to ensuring equal access and providing reasonable accommodations to qualified individuals with disabilities upon request. To request this document in an alternate format or to seek a reasonable accommodation, please contact the Department of Accessibility Services at accessibility@emory.edu or call 404-727-9877 (Voice) | 404-712-2049 (TDD). We kindly ask that requests be made at least seven business days in advance to allow adequate time for coordination.
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Benefits
Hours and flexibility
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About Emory Health
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Hospitals
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10,000+ Employees
Headquarters location
NE Atlanta, GA, US
Year founded
1905