Top 25 Clinical trial manager Jobs in Georgia

Manager, Clinical Research Monitoring
Edwards Lifesciences —Georgia
- $126,000 - $178,000 a year
- Full-time
- Anatomy knowledge
- Analysis skills
- Bachelor's degree
Project Manager I PDC
Atrium Health —Macon, GA
- $30.70 - $46.05 an hour
- Full-time
- Construction site
- Hospital
- Ability to walk for extended periods
- Paid parental leave
- Disability insurance
9d
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
Manager- Clinical Research Operations
Northside Hospital Inc. —Atlanta, GA
- Full-time
- 5 years
- Analysis skills
- Bachelor's degree
Clinical Project Manager - Oncology (Client Dedicated/Remote)
サイネオス・ヘルス —Georgia
- $120,000 - $135,000 a year
- Remote
- Mid-level
- 3 years
- Bachelor's degree
- Employee stock purchase plan
- Health insurance
Senior Data Team Lead (Remote)
IQVIA —Atlanta, GA
- $86,800 - $217,100 a year
- Full-time
- Remote
- 7 years
- Bachelor's degree
- Continuous improvement
- Health insurance
- Dental insurance
Clinical Trials Manager - School of Medicine, Nephrology
Emory University —Atlanta, GA
- Full-time
- Hybrid work
- Master's degree
- University
- Bachelor's degree
- Work from home
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
10d
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
Research Project Coordinator Supervisor- School of Medicine, Emergency Medicine
Emory University —Decatur, GA
- Full-time
- Hybrid work
- Nursing
- Management
- Mid-level
- Work from home
6d
Project Lead - RUA92307
IQVIA —Atlanta, GA
- $200,000 - $225,000 a year
- Full-time
- Nursing
- Driver's License
- Travel
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
12d
Clinical Research Site - Office Manager
Global Research Associates —Stockbridge, GA
- $58,000 - $62,400 a year
- Full-time
- Mid-level
- 3 years
- Organizational skills
- Paid holidays
- Health insurance
Quick Apply
6d
Monitoring Oversight Lead (Lead CRA)
Artivion —Kennesaw, GA
- Remote
- Data entry
- Recruiting
- Senior level
Quick Apply
Clinical Research Nurse (RN) Manager - Atrium Health Navicent Trauma Services
Atrium Health —Macon, GA
- $47.50 - $71.25 an hour
- Full-time
- Nursing
- RN License
- Customer service
- Paid parental leave
- Disability insurance
Regional Research Manager
DAVITA —Columbus, GA
- Weekends as needed
- Bachelor of Science
- Mid-level
- Office
- Health insurance
- Dental insurance
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
Clinical Laboratory Supervisor - Atrium Health Baldwin - Evenings
Atrium Health —Milledgeville, GA
- $41.10 - $61.65 an hour
- Overnight shift
- Hospital
- Customer service
- 3 years
- Paid parental leave
- Disability insurance
Supervisor Laboratory Operations (Non-Clinical) - Atrium Health Peach
Atrium Health —Byron, GA
- $30.70 - $46.05 an hour
- Weekends as needed
- Hospital
- Customer service
- 3 years
- Paid parental leave
- Disability insurance
Research Manager - MCG Physiology
Augusta University —Augusta, GA
- $62,300 - $79,400 a year
- Full-time
- Background check
- Master's degree
- University
- Paid holidays
- Health insurance

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Manager, Clinical Research Monitoring

Edwards Lifesciences -
Georgia

Apply Now

Job Details

Full-time
$126,000 - $178,000 a year

Qualifications

Clinical audit and monitoring
Quality control management
Research regulatory compliance
Quality assurance experience within healthcare

Full Job Description

Imagine how your ideas and expertise can change a patient’s life. We generate extensive clinical evidence to demonstrate the effectiveness and safety of our innovations and how our products transform patients’ lives. As part of our Clinical Affairs team, you’ll hone your scientific curiosity and passion for evaluating data to increase access to pioneering technologies for patients in need. In close partnership with principal investigators, dedicated medical professionals, patient advocacy groups, and regulatory authorities, you will drive the evidence needed to optimize patient outcomes.

Aortic stenosis impacts millions of people globally, yet it often remains under-diagnosed and under-treated. Edwards’ groundbreaking work in transcatheter aortic heart valve replacement (TAVR) pioneered an innovative, life-changing solution for patients by offering heart valve replacement without the need for open heart surgery. Our Transcatheter Heart Valve (THV) business unit continues to partner with cardiologists and clinical teams to transform patient care with devices supported by clinical evidence. It’s our driving force to help patients live longer and healthier lives. Join us and be part of our inspiring journey.

How you will make an impact:

Providing input on strategic direction on field monitoring of studies and data collection for clinical trials with increased volume and complexity (e.g., KOL site), acting as a Core Team lead, assessing all data documentation, reports, records, transcripts, exam results for consistency with case report form, and determining if clinical trial/study subject documentation is within parameters of study hypothesis, as well as monitoring clinical trial/study safety, in keeping with protocols, GCP (Good Clinical Practices) and regulatory requirements.
Participating and contributing to the development of clinical protocols, informed consent forms, and case report forms.
Leading in the development of technical training on GCPs, protocols, database, compliance, device accountability, adverse event reporting, study investigation protocols, amendments, regulatory documentation requirements as well as training and proctoring new employees on trial and study related activities. Acting as a mentor to new or junior level employees.
Providing direction and guidance to execute project deliverables in collaboration with project managers.
Identifying and evaluating clinical process improvement opportunities.
Overseeing clinical trial conduct including management of metrics (e.g., dashboard), compliance, protocol deviations, and data entry cadence.
Participating in the development and validation of case report forms.
Reviewing monitoring visit reports.
Resolving complex trial/study data and regulatory documentation discrepancies escalated by junior level employees.
Reviewing and completing checklist on informed consent forms (ICF).

What you’ll need (Required):

Bachelor's Degree or equivalent in related field with 8 years of field monitoring, quality assurance/control and regulatory compliance experience or equivalent work experience based on Edwards criteria.

What else we look for (Preferred):

Experience working in a medical device or regulated industry
Clinical research certification (ACRP or SoCRA clinical coordinator / CRA certification)
Proven expertise in MS Office Suite, including Word, Excel, Adobe, and ability to operate general computer software and office machinery
Experience with electronic data capture
Excellent written and verbal communication skills including negotiating and relationship management skills with ability to drive achievement of objectives
Excellent problem-solving, organizational, analytical and critical thinking skills
Extensive knowledge and understanding of Edwards policies, procedures, and international and domestic medical device regulatory guidelines relevant to clinical studies
Extensive understanding of cardiovascular anatomy, pathology and physiology or Business Unit area of expertise
Strong leadership skills and ability to influence change
Ability to manage confidential information with discretion
Strict attention to detail
Ability to interact professionally with all organizational levels
Ability to manage competing priorities in a fast-paced environment
Must be able to work in a team environment, including serving as consultant to management
Ability to interact with suppliers, vendors and/or customers

Aligning our overall business objectives with performance, we offer competitive salaries, performance-based incentives, and a wide variety of benefits programs to address the diverse individual needs of our employees and their families.

The base pay range for this position is $126,000 to $178,000 (highly experienced).

The pay for the successful candidate will depend on various factors (e.g., qualifications, education, prior experience). Applications will be accepted while this position is posted on our Careers website.

E dwards is an Equal Opportunity/Affirmative Action employer including protected Veterans and individuals with disabilities.

COVID Vaccination Requirement

Edwards is committed to protecting our vulnerable patients and the healthcare providers who are treating them. As such, all patient-facing and in-hospital positions require COVID-19 vaccination. If hired into a covered role, as a condition of employment, you will be required to submit proof that you have been vaccinated for COVID-19, unless you request and are granted a medical or religious accommodation for exemption from the vaccination requirement. This vaccination requirement does not apply in locations where it is prohibited by law to impose vaccination.

Apply Now

Refine Your Search

clinical trial manager jobs in georgia

Manager, Clinical Research Monitoring

Project Manager I PDC

Associate Clinical Site Lead - Atlanta

Manager- Clinical Research Operations

Clinical Project Manager - Oncology (Client Dedicated/Remote)

Senior Data Team Lead (Remote)

Clinical Trials Manager - School of Medicine, Nephrology

Principal Field Clinical Lead - Atlanta, GA

Clinical Project Lead, Oncology

Research Project Coordinator Supervisor- School of Medicine, Emergency Medicine

Project Lead - RUA92307

Sr. Manager, Medical Field

Clinical Research Site - Office Manager

Monitoring Oversight Lead (Lead CRA)

Clinical Research Nurse (RN) Manager - Atrium Health Navicent Trauma Services

Regional Research Manager

Team Lead Research Coordinator- General Hematology & Hemostasis and Thrombosis

Clinical Laboratory Supervisor - Atrium Health Baldwin - Evenings

Supervisor Laboratory Operations (Non-Clinical) - Atrium Health Peach

Research Manager - MCG Physiology

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