Top 21 Clinical research manager Jobs in Duluth, Ga

Clinical Research Manager
GI Care For Kids —Sandy Springs, GA
- Microsoft Excel
- Microsoft Outlook
- Inventory management
Quick Apply
6d
Manager- Clinical Research Operations
Northside Hospital Inc. —Atlanta, GA
- Full-time
- 5 years
- Analysis skills
- Bachelor's degree
Clinical Research Engagement Lead - South Region (Atlanta, GA)
Genentech —Atlanta, GA
- $108,800 - $202,000 a year
- Online Application
- Bachelor of Science
- Bachelor's degree
- Doctor of Philosophy
Clinical Trials Manager - School of Medicine, Nephrology
Emory University —Atlanta, GA
- Full-time
- Hybrid work
- Master's degree
- Bachelor's degree
- Data entry
- Work from home
Clinical Research Manager
United Digestive —Atlanta, GA
- Full-time
- Nursing
- 5 years
- Pass drug screening
Quick Apply
6d
Research Project Coordinator Supervisor- School of Medicine, Emergency Medicine
Emory University —Decatur, GA
- Full-time
- Hybrid work
- Nursing
- Management
- Mid-level
- Work from home
Project Lead - RUA92307
IQVIA —Atlanta, GA
- $200,000 - $225,000 a year
- Full-time
- Nursing
- Driver's License
- Travel
12d
Clinical Trial Material Manager (2nd Shift)
IQVIA —Marietta, GA
- $77,700 - $161,800 a year
- Overtime
- Microsoft Outlook
- Office
- Bachelor's degree
Research Project Manager - Rollins School of Public Health
Emory University —Atlanta, GA
- Full-time
- Hybrid work
- Mid-level
- University
- Team management
- Work from home
Senior Laboratory Project Services Manager
IQVIA —Marietta, GA
- $83,000 - $173,000 a year
- Full-time
- Remote
- Computer literacy
- Laboratory experience
- English
- Work from home
19h
Principal Field Clinical Lead - Atlanta, GA
Abbott Laboratories —Atlanta, GA
- $99,300 - $198,700 a year
- Weekends as needed
- Nursing
- Up to 50% travel
- 5 years
- Health insurance
- Tuition reimbursement
Clinical Project Lead, Oncology
IQVIA —Atlanta, GA
- $68,400 - $232,800 a year
- Full-time
- Remote
- 3 years
- Bachelor's degree
- Senior level
- Work from home
Associate Clinical Site Lead - Atlanta
Abbott Laboratories —Atlanta, GA
- $50,700 - $101,300 a year
- Full-time
- Nursing
- Engineering
- Mid-level
- Health insurance
- Tuition reimbursement
Senior Project Manager, LV & eCOA
IQVIA —Atlanta, GA
- $78,700 - $196,800 a year
- Full-time
- Remote
- Customer service
- 5 years
- Bachelor's degree
- Work from home
1d
Research Project Manager
CORPORATE TEMPS —Winder, GA
- $21 - $23 an hour
- Part-time
- Supervising experience
- Organizational skills
- In-person
Quick Apply
2d
Sr. Manager, Medical Field
Taiho Oncology, Inc. —Atlanta, GA
- $178,500 - $210,000 a year
- Full-time
- Medicine
- Writing skills
- English
- Paid time off
- Parental leave
Quick Apply
Clinical Domain Project Manager (PBM)
Briljent —Atlanta, GA
- Urgently hiring
- Remote
- Background check
- 7 years
- Continuous improvement
- AD&D insurance
- Disability insurance
Quick Apply
7d
Team Lead Research Coordinator- General Hematology & Hemostasis and Thrombosis
Children's Healthcare of Atlanta —Brookhaven, GA
- Full-time
- Mid-level
- Bachelor's degree
- Children
- On-the-job training
Quick Apply

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Research Project Manager
CORPORATE TEMPS —Winder, GA
Strong knowledge of data collection methods, statistical analysis for research purposes, and research data management tools such as Microsoft Office Suite.
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As a Commercial Project Manager, you will be an integral part of the project management team supporting strategic initiatives and operational excellence.
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Clinical Research Manager

GI Care For Kids -
Sandy Springs, GA

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Job Details

6 days ago

Qualifications

Managing projects

Full Job Description

GI Care for Kids is hiring a Clinical Research Manager.
The Clinical Research Manager is responsible for supporting the needs of the clinical research department and the investigators. The Clinical Research Manager ensures that research conducted at the site is performed and conducted with highest ethical standards and adheres to all GCP and FDA standards. Along with managing the Clinical Research department, the Clinical Research Manager is expected to be able to conduct duties of a clinical research coordinator.

Essential Duties

The Clinical Research Manager is the main point of contact with sponsors, CRO’s, and Laboratories.
Reviews and completes Budget negotiations with sponsors and CRO’s for upcoming and active studies at the site.
Coordinates with sponsors, CRO’s and GI Care for Kids’ legal team to ensure that clinical trial agreements are completed and executed in a timely fashion.
Completes regulatory submission for study start up.
Enters studies and budgets into the clinical trial management system.
Coordinates with the practice bookkeeper that financials for the research department are ac-curate and ensures payment receipts.
Coordinates with all departments of the practice to ensure that the Research Department follows and abides by the SOPs of the Practice.
Creates and updates SOPs for the Clinical Research Department as needed.
Communicates with physicians and staff on a regular basis regarding current research studies.
Ensures all participating physicians’ trainings and certifications for research are current and up to date.
Creates relationships with nearby physician practices and vendors for requirements of study protocols.
Analyzes and reads protocols to determine if the protocols are suitable for the practice.
Completes feasibility questionnaires for upcoming studies.
Works with the physicians in the practice to determine interests in studies.
Works with the coordinators and research staff to ensure that study enrollment goals are met according to contracts.
Implements recruitment procedures to ensure enrollment goals are met per contract.
Creates and sends invoices to sponsors.
Ensures vendors for research projects are compensated.
Schedules and coordinates site initiation visits with sponsors and PI.
Ensuring all equipment for studies are calibrated and maintained.
Serves as a back-up to coordinators.
Coordinates with Principal Investigator and department to help ensure that clinical research and related activities are performed in accordance with ICH and GCP guidelines.
Assists the in development of materials and tools necessary to appropriately train individuals involved in the conduct of the study around issues related to (but not limited to) protocol re-quirements, schedule of visits, execution of research plan. Maintains documentation of train-ing.
Assists Principal Investigator to assure that all key personnel or persons ‘engaged’ in the re-search project have met training requirements.
Coordinates and facilitates monitoring and auditing visits.
Collaborates with PI and institution to respond to any audit findings and implement approved recommendations.
Reviews and comprehends the protocol.
Attends investigator meetings as required or requested.
Prepares and submits any IRB and any other regulatory submission documents as required by the protocol.
Prepares other study materials as required. These study materials include, but are not limited to, the informed consent document, case report forms (CRFs), enrollment logs, and drug/device accountability logs.
Establishes and organizes study files, including but not limited to, regulatory binders, study specific source documentation and other materials.
Reviews and develops a familiarity with the protocol, e.g., study proceedings and timelines, inclusion and exclusion criteria, confidentiality, privacy protections.
Assists PI in communication of study requirements to all individuals involved in the study. Pro-vides appropriate training and tools for study team members. Documents date of training and signatures of study personnel trained on study specific training log.
Works with other members of the research staff to develop and implement recruitment strategies in accordance with IRB requirements and approvals.
Screens subjects for eligibility using protocol specific inclusion and exclusion criteria, documenting each potential participant’s eligibility or exclusion.
Coordinates research subjects’ tests and procedures.
Collects data as required by the protocol. Assures timely completion of Case Report Forms.
Maintains study timelines.
Maintains adequate inventory of study supplies.
Completes study documentation and maintains study files in accordance with sponsor and regulatory requirements.
Retains all study records in accordance with sponsor and regulatory requirements.
Maintains effective and ongoing communication with sponsor, research participants and PI during the course of the study.
Process and collect lab samples according to IATA guidelines.
Adheres to GCP and ICH guidelines at all times.

Supervisory Guidelines

Supervises clinical research coordinators and research assistants
Guides and trains Clinical Research staff
Ensures staff are completing study visits within windows and data entry is being completed with CTA windows
Training of New employees
Conducting regular meetings with staff to ensure departments needs and requirements are met.
Completing annual evaluations of research staff
Ensuring staff are using payroll system to maintain accurate records of time worked
Making sure that the research staff are maintaining a clean and safe work environment
Ensuring staff are following IATA in the processing and shipping of Biologic
Ensuring staff Certifications are up to date and current

Education, Experience, KSAs

Bachelor’s Degree or higher
Excellent verbal and written communication skills.
Proficient in Microsoft Office suite—Word, Excel, PowerPoint, Outlook and Visio.
Professional appearance and demeanor.
Versatility, flexibility, and a willingness to work with enthusiasm within constantly changing priorities.
Acute attention to detail.
Commitment to excellence and high standards.
Ability to work on complex projects with general direction and minimal guidance.
Ability to deal effectively with a diversity of individuals at all organizational levels.
Good judgement with the ability to make timely and sound decisions
Creative, flexible, and innovative team player
Strong organizational, problem-solving, and analytical skills; able to manage priorities and workflow.
Ability to work independently and as a member of a team.
Demonstrated ability to plan and organize projects.

Competencies

Ethics - Treats people with respect; keeps commitments; inspires the trust of others; works with integrity and ethically; upholds organizational values.
Adaptability - Adapts to changes in the work environment; manages competing demands; changes ap-proach or method to best fit the situation; able to deal with frequent change, delays, or unexpected events.
Customer Service - Manages difficult sponsors; responds promptly to sponsor needs; responds to re-quests for service and assistance; meets commitments.
Interpersonal Skills - focuses on solving conflict, not blaming; maintains confidentiality; listens to others without interrupting; keeps emotions under control; remains open to others' ideas and tries new things.
Organizational Support- Follows policies and procedures; completes research tasks correctly and on time; supports organization's goals and values; benefits organization through outside activities; sup-ports affirmative action and respects diversity.
Teamwork - Balances team and individual responsibilities; exhibits objectivity and openness to others' views; gives and welcomes feedback; contributes to building a positive team spirit; puts success of team above own interests; able to build morale and group commitments to goals and objectives; sup-ports everyone's efforts to succeed.

Physical Demands and Work Environment

Frequent sitting, standing, walking, grasping, carrying and speaking
Occasional reaching, bending and stooping
Lifting, carrying, pushing and pulling up to 50 pounds, with assistance if needed.
Frequent use of computer, keyboard, copy/fax machine, and phone
Possible exposure to infectious specimens (blood or bodily fluids or airborne pathogens).
May be required to wear Personal Protective Equipment (PPE).
While performing the duties of this job, the noise level in the work environment is usually quiet to moderate.
Fast paced environment with occasional high pressure or emergent situations.
Work hours subject to office needs to ensure coverage during all hours of operation.

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clinical research manager jobs in duluth, ga

Clinical Research Manager

Manager- Clinical Research Operations

Clinical Research Engagement Lead - South Region (Atlanta, GA)

Clinical Trials Manager - School of Medicine, Nephrology

Clinical Research Manager

Research Project Coordinator Supervisor- School of Medicine, Emergency Medicine

Project Lead - RUA92307

Clinical Trial Material Manager (2nd Shift)

Research Project Manager - Rollins School of Public Health

Senior Laboratory Project Services Manager

Principal Field Clinical Lead - Atlanta, GA

Clinical Project Lead, Oncology

Associate Clinical Site Lead - Atlanta

Senior Project Manager, LV & eCOA

Research Project Manager

Sr. Manager, Medical Field

Clinical Domain Project Manager (PBM)

Team Lead Research Coordinator- General Hematology & Hemostasis and Thrombosis

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