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Clinical Trial Jobs in Decatur, GA (NOW HIRING)

Wellstar Health System

RN Research Coordinator

Marietta, GA · On-site

$65K - $81K/yr

Coordinates all facets of patient involvement in clinical trials. - Conducts all aspects of clinical trial, including consenting, using Good Clinical Practice, FDA, and Institutional guidelines ...

YO AI Labs

Biostatistician Expert - Remote

Atlanta, GA · Remote

$60 - $70/hr

Analyze and validate clinical trial data. * Review and interpret Statistical Analysis Plans (SAPs). * Produce and quality-check Tables, Figures & Listings (TFLs). * Review Clinical Study Reports ...

YO AI Labs

Hematology Expert - Remote

Atlanta, GA · Remote

$150 - $200/hr

Analyze clinical study reports, safety reports, regulatory documents, and trial materials to assess medical accuracy. * Evaluate the clinical relevance of efficacy and safety conclusions, including ...

YO AI Labs

Oncology Expert - Remote

Atlanta, GA · Remote

$150 - $200/hr

Analyze clinical study reports, safety reports, regulatory documents, and trial materials to assess medical accuracy. * Evaluate the clinical relevance of efficacy and safety conclusions, including ...

Denali Health

Clinical Research Coordinator III

Atlanta, GA · On-site

$23.25 - $31/hr

Experience with EDC systems and clinical trial management software preferred. * CCRC/CCRP ... certification a plus. Why Join Denali Health: * Work with a mission-driven team advancing clinical ...

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All JobsClinical Trial JobsClinical Trial Jobs in Decatur, GA

Clinical Trial information

See Decatur, GA salary details

$28

$61

$93

How much do clinical trial jobs pay per hour?

As of Aug 21, 2026, the average hourly pay for clinical trial in Decatur, GA is $61.04, according to ZipRecruiter salary data. Most workers in this role earn between $49.52 and $68.75 per hour, depending on experience, location, and employer.

What are clinical trials?

Clinical trials are research studies that involve human participants and are designed to evaluate the safety and effectiveness of new medical treatments, drugs, or devices. These trials follow a carefully controlled protocol and are conducted in phases to systematically assess outcomes. Participants may include patients with specific medical conditions or healthy volunteers, depending on the study's goals. The results from clinical trials help inform medical decisions and regulatory approvals for new therapies.

What are the key skills and qualifications needed to thrive in a clinical trial role?

To thrive in a Clinical Trial role, you need a solid understanding of clinical research principles, regulatory compliance, and data management, usually supported by a degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) certification, and clinical trial management software is typically required. Strong attention to detail, organizational abilities, and effective communication skills help professionals coordinate complex processes and collaborate with interdisciplinary teams. These competencies are vital to ensure trials are conducted ethically, efficiently, and in compliance with regulatory standards.

What are some common challenges faced by professionals working in clinical trial management, and how can they be addressed?

Professionals in clinical trial management often encounter challenges such as adhering to strict regulatory requirements, managing complex timelines, and ensuring effective communication among multidisciplinary teams. Overcoming these challenges typically involves thorough planning, continuous training on regulatory updates, and the use of project management tools to track progress and coordinate tasks. Building strong relationships with investigators and fostering open communication can also help address issues quickly and maintain trial integrity.

How to get into a clinical trial career?

A career in clinical trials typically requires a background in healthcare, life sciences, or related fields, along with knowledge of Good Clinical Practice (GCP) guidelines. Entry-level roles often require a bachelor's degree, and certifications such as Certified Clinical Research Professional (CCRP) can enhance job prospects. Gaining experience through internships or entry-level positions in research settings is also beneficial.

What jobs are there in clinical trials?

Jobs in clinical trials include clinical research coordinators, clinical research associates, data managers, regulatory affairs specialists, and study nurses. These roles involve tasks such as patient recruitment, data collection, monitoring trial progress, and ensuring compliance with regulations, often requiring knowledge of Good Clinical Practice (GCP) and relevant certifications. The work environment is typically in hospitals, research centers, or pharmaceutical companies.

What are the most commonly searched types of Clinical Trial jobs in Decatur, GA?

The most popular types of Clinical Trial jobs in Decatur, GA are:

What are popular job titles related to Clinical Trial jobs in Decatur, GA?

For Clinical Trial jobs in Decatur, GA, the most frequently searched job titles are:

What job categories do people searching Clinical Trial jobs in Decatur, GA look for?

The top searched job categories for Clinical Trial jobs in Decatur, GA are:

What cities near Decatur, GA are hiring for Clinical Trial jobs?

Cities near Decatur, GA with the most Clinical Trial job openings:

Clinical Trial jobs near you
Infographic showing various Clinical Trial job openings in Decatur, GA as of August 2026, with employment types broken down into 67% Full Time, and 33% Part Time. Highlights an 74% In-person, and 26% Remote job distribution, with an average salary of $126,957 per year, or $61 per hour.

Principal Field Clinical Lead - Atlanta, GA

Abbott

Atlanta, GA • On-site

Full-time

Medical, Retirement

This job post has expired today. Applications are no longer accepted.

Abbott rating

7.8

Company rating: 7.8 out of 10

Based on 138 frontline employees who took The Breakroom Quiz

175th of 543 rated manufacturers

Job description

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 115,000 colleagues serve people in more than 160 countries.
JOB DESCRIPTION:
Principal Field Clinical Lead
Working at Abbott
At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life. You'll also have access to:
  • Career development with an international company where you can grow the career you dream of.
  • Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year.
  • An excellent retirement savings plan with a high employer contribution
  • Tuition reimbursement, the Freedom 2 Save student debt program, and FreeU education benefit - an affordable and convenient path to getting a bachelor's degree.
  • A company recognized as a great place to work in dozens of countries worldwide and named one of the most admired companies in the world by Fortune.
  • A company that is recognized as one of the best big companies to work for as well as the best place to work for diversity, working mothers, female executives, and scientists.

The Opportunity
Within Abbott's Structural Heart business, our mission is to restore health and improve quality of life through innovative solutions for the treatment of structural heart disease. We are committed to developing technologies that improve patient outcomes, advance clinical practice, and provide meaningful benefits for physicians, healthcare systems, and the patients they serve.
As a global leader in transcatheter heart valve technologies, Abbott continues to invest in clinical research, physician education, and next-generation therapies that shape the future of structural heart interventions.
Abbott Structural Heart is seeking a highly experienced Principal Field Clinical Lead (FCL) to support pre-market and post-market Transcatheter Aortic Valve Implantation (TAVI) clinical studies within an assigned territory.
In this senior clinical role, the Principal FCL serves as a key partner to physicians, study investigators, research coordinators, and internal stakeholders to ensure successful clinical trial execution, exceptional patient outcomes, and high-quality clinical data.
The Principal FCSL functions as a clinical and procedural expert, providing physician education, procedural support, site management, enrollment strategy, and clinical trial leadership. This individual will also contribute to the development of future TAVI technologies by partnering with Clinical Affairs, Research & Development, Engineering, and Commercial teams to advance Abbott's structural heart portfolio.
Success in this role requires a deep understanding of structural heart disease, transcatheter valve therapies, clinical research operations, and physician training within Cath Lab and Hybrid Operating Room environments.
What You'll Work On
Clinical Trial Leadership & Site Management
  • Manage and develop strategic relationships with assigned clinical trial sites, investigators, and research teams.
  • Support all phases of clinical trial execution, including site identification, qualification, activation, enrollment, monitoring, and study closeout activities.
  • Collaborate with investigators and site personnel to maximize patient screening opportunities and achieve enrollment objectives.
  • Identify enrollment barriers and implement solutions that improve patient recruitment and study performance.
  • Maintain a comprehensive understanding of site capabilities, research infrastructure, and investigator interests to support Abbott's clinical evidence generation strategy.
  • Facilitate communication between clinical sites and Abbott teams to ensure efficient study execution and issue resolution.

TAVI Clinical and Procedural Support
  • Serve as a subject matter expert for Abbott's TAVI clinical programs and investigational technologies.
  • Provide procedural guidance and technical support during investigational TAVI procedures.
  • Support physicians and healthcare teams in procedural planning, device utilization, and study protocol adherence.
  • Partner with commercial field teams when additional procedural expertise is required.
  • Ensure proper application of study protocols and eligibility criteria for patient selection.
  • Maintain expertise in current and emerging structural heart therapies, competitive technologies, and evolving treatment strategies.

Physician and Clinical Staff Education
  • Design and deliver educational programs for physicians, research coordinators, physician assistants, nurses, and Cath Lab personnel.
  • Train healthcare professionals on investigational devices, clinical protocols, procedural best practices, and study requirements.
  • Develop educational content and presentation materials for:
    • Investigator Meetings
    • National and regional conferences
    • Physician training programs
    • Internal educational initiatives
    • Serve as a trusted clinical resource for both internal and external stakeholders.

Clinical Evidence and Research Support
  • Support the generation and dissemination of clinical evidence related to Abbott's TAVI portfolio.
  • Effectively communicate clinical data, trial objectives, and evidence-based recommendations to healthcare professionals.
  • Collaborate with Global Clinical Affairs and Medical Affairs teams to support ongoing and future research initiatives.
  • Assist in identifying opportunities to improve study design, enrollment strategies, and overall trial performance.
  • Promote diverse and representative patient enrollment across clinical trials.

Product Development and Innovation
  • Partner with Engineering, Clinical Affairs, and Product Development teams to support next-generation TAVI platform development.
  • Provide real-world clinical insights that inform product design enhancements and future innovation efforts.
  • Participate in pre-clinical and clinical evaluations of emerging technologies.
  • Assist in developing procedural best practices for new platform introductions and early-stage clinical evaluations, including:
    • First-in-Human Studies
    • Early Feasibility Studies
    • IDE Clinical Trials

Leadership and Mentorship
  • Mentor and develop less-experienced Field Clinical Leads.
  • Share best practices and support the ongoing development of field clinical teams.
  • Provide leadership across cross-functional projects and initiatives.
  • Assist management with onboarding, coaching, and development of clinical personnel as needed.
  • Identify opportunities for operational improvements and process standardization across the organization.

Compliance and Quality
  • Conduct all activities in accordance with:
    • FDA regulations
    • Good Clinical Practice (GCP) guidelines
    • Company policies and procedures
    • Quality system requirements
    • Clinical study protocols
  • Maintain all required certifications and training for assigned product lines and study processes.
  • Ensure accurate and timely documentation and communication of clinical activities.
  • Foster professional and collaborative relationships with customers, physicians, investigators, and internal partners

This position works closely with / Cross-functional Partnerships:
  • Global Clinical Affairs (GCA)
  • Medical Directors
  • Program Management Teams
  • Global Clinical Organization (GCO)
  • Research & Development
  • Engineering
  • Marketing
  • Medical Affairs
  • Commercial Structural Heart Teams

The role also requires significant interaction with:
  • Interventional Cardiologists
  • Cardiac Surgeons
  • Study Investigators
  • Research Coordinators
  • Cath Lab Staff
  • Physician Assistants
  • Nurse Practitioners
  • Registered Nurses

Required Qualifications
Education
  • Associate degree with 13+ years of relevant experience, or
  • Bachelor's degree with 10+ years of relevant experience, or
  • Master's degree or advanced degree with 5+ years of relevant experience.

Relevant disciplines include:
  • Biological Sciences
  • Health Sciences
  • Nursing
  • Biomedical Engineering
  • Clinical Research
  • Other related healthcare or scientific fields

Experience
  • Significant experience supporting implants and procedures involving complex transcatheter valve technologies.
  • Extensive experience within a structural heart or transcatheter valve medical device organization.
  • Previous experience providing physician and healthcare staff training on advanced cardiovascular procedures.
  • Minimum of 4 years of clinical research experience, preferably within Field Clinical Affairs or Medical Device Clinical Operations.
  • Strong understanding of:
    • TAVI/TAVR procedures
    • Clinical trial execution
    • Cath Lab workflows
    • Hybrid Operating Room environments
    • Structural heart disease therapies
  • Experience managing physician relationships and supporting high-volume clinical centers.

Knowledge, Skills & Competencies
  • Deep clinical and procedural knowledge of structural heart therapies.
  • Exceptional presentation and physician training skills.
  • Strong leadership and mentoring capabilities.
  • Ability to influence without direct authority.
  • Excellent written and verbal communication skills.
  • Strong organizational and project management abilities.
  • Ability to work independently while effectively collaborating across cross-functional teams.
  • Skilled at managing multiple priorities in a fast-paced environment.
  • High attention to detail and commitment to quality.
  • Ability to build credibility and trust with physicians, investigators, and internal stakeholders.

Travel Requirements
  • Ability and willingness to travel approximately 50% to 75%, including overnight travel as required. US and OUS
  • Flexibility to support physician and customer needs outside standard business hours, including occasional evenings and weekends.

Apply Now
Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives: www.abbottbenefits.com
Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity.
Connect with us at www.abbott.com, on Facebook at www.facebook.com/Abbott, and on X @AbbottNews.
The base pay for this position is
$99,300.00 - $198,700.00
In specific locations, the pay range may vary from the range posted.
JOB FAMILY:
Clinical Affairs / Statistics
DIVISION:
SH Structural Heart
LOCATION:
United States of America : Remote
ADDITIONAL LOCATIONS:
WORK SHIFT:
Standard
TRAVEL:
Yes, 75 % of the Time
MEDICAL SURVEILLANCE:
Yes
SIGNIFICANT WORK ACTIVITIES:
Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day), Continuous standing for prolonged periods (more than 2 consecutive hours in an 8 hour day), Keyboard use (greater or equal to 50% of the workday), Lift, carry, push or pull weights of more than 20 pounds/9 kilos on a regular/daily basis
Abbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans.
EEO is the Law link - English: http://webstorage.abbott.com/common/External/EEO_English.pdf
EEO is the Law link - Espanol: http://webstorage.abbott.com/common/External/EEO_Spanish.pdf

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