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Clinical Research Director Jobs in Rome, GA (NOW HIRING)

Direct connection with Army physicians Beyond Your MD: * Leadership from Day One: By the time you ... Clinical Excellence: Access to training at premier military medical facilities with complex cases ...

Direct connection with Army physicians Beyond Your MD: * Leadership from Day One: By the time you ... Clinical Excellence: Access to training at premier military medical facilities with complex cases ...

Direct connection with Army physicians Beyond Your MD: * Leadership from Day One: By the time you ... Clinical Excellence: Access to training at premier military medical facilities with complex cases ...

Direct connection with Army physicians Beyond Your MD: * Leadership from Day One: By the time you ... Clinical Excellence: Access to training at premier military medical facilities with complex cases ...

Direct connection with Army physicians Beyond Your MD: * Leadership from Day One: By the time you ... Clinical Excellence: Access to training at premier military medical facilities with complex cases ...

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Clinical Research Director information

See Rome, GA salary details

$10

$54

$116

How much do clinical research director jobs pay per hour?

As of Aug 20, 2026, the average hourly pay for clinical research director in Rome, GA is $54.36, according to ZipRecruiter salary data. Most workers in this role earn between $32.45 and $71.68 per hour, depending on experience, location, and employer.

What does a clinical research director do?

A clinical research director manages medical or pharmaceutical research projects. In this role, you may oversee a research department at a university or medical facility. Your specific job duties vary, depending on the type of project you work on, but your general responsibilities include overseeing the planning stages of each research project or clinical trial, discussing outcomes and expectations with researchers, making sure that research staff members provide the proper care to participants in the trial or research project, and ensuring that data is documented properly. Clinical research directors also hire and train new staff members and check that the project follows all governmental and industry guidelines.

What are the responsibilities of a clinical research director?

A Clinical Research Director oversees the planning, coordination, and management of clinical trials and research projects within healthcare or pharmaceutical organizations. They ensure studies comply with regulatory requirements, establish research protocols, manage budgets, and supervise research teams. Additionally, they collaborate with stakeholders, analyze data, and ensure that clinical trials are conducted ethically and efficiently to advance medical knowledge and patient care.

What are the key skills and qualifications needed to thrive as a clinical research director, and why are they important?

To thrive as a Clinical Research Director, you need advanced knowledge of clinical trial design, regulatory compliance, and data analysis, typically supported by a medical, pharmaceutical, or life sciences degree along with significant experience in clinical research. Expertise in systems such as electronic data capture (EDC), clinical trial management systems (CTMS), and familiarity with GCP, FDA, and ICH guidelines are essential, and certifications like CCRP or CCRA are highly valued. Leadership, strategic thinking, and strong communication skills distinguish top performers by enabling effective team management and stakeholder engagement. These competencies ensure that clinical trials are conducted ethically, efficiently, and in compliance with all regulatory standards, driving successful research outcomes.

What are some of the main challenges a clinical research director faces when overseeing multiple clinical trials simultaneously?

One of the primary challenges for a Clinical Research Director managing multiple trials is ensuring consistent protocol adherence across diverse study sites while maintaining strict regulatory compliance. Balancing resource allocation, addressing unforeseen issues such as patient recruitment delays, and effectively communicating with cross-functional teams also require strong organizational and leadership skills. Additionally, the director must stay updated on evolving industry standards and regulatory requirements to mitigate risks and ensure the integrity of all ongoing studies.

What is the difference between Clinical Research Director vs Clinical Research Manager?

AspectClinical Research DirectorClinical Research Manager
ResponsibilitiesOversees multiple projects, strategic planning, and department leadershipManages daily operations of clinical trials, supervises teams, and ensures compliance
Required CredentialsTypically requires a PhD, MD, or advanced degree, along with extensive experienceUsually requires a bachelor's or master's degree in life sciences, with relevant experience
Work EnvironmentSenior leadership in pharmaceutical or biotech companies, overseeing multiple teamsOperational setting within research sites or CROs, directly managing trial teams
Industry UsageCommonly found in large organizations with multiple projectsFound in both large and small organizations, focusing on trial execution

The Clinical Research Director focuses on strategic oversight and leadership of research programs, while the Clinical Research Manager handles day-to-day trial management. Both roles require relevant experience, but the director's role is more senior and strategic.

What are the most commonly searched types of Clinical Research jobs in Rome, GA?

The most popular types of Clinical Research jobs in Rome, GA are:

What are popular job titles related to Clinical Research Director jobs in Rome, GA?

For Clinical Research Director jobs in Rome, GA, the most frequently searched job titles are:

What job categories do people searching Clinical Research Director jobs in Rome, GA look for?

The top searched job categories for Clinical Research Director jobs in Rome, GA are:

What cities near Rome, GA are hiring for Clinical Research Director jobs?

Cities near Rome, GA with the most Clinical Research Director job openings:

Infographic showing various Clinical Research Director job openings in Rome, GA as of August 2026, with employment types broken down into 2% As Needed, 68% Full Time, 22% Part Time, 7% Contract, and 1% Nights. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $113,061 per year, or $54.4 per hour.

Clinical Research Coordinator - Oncology Gordon and Redmond

AdventHealth

Calhoun, GA

$42K - $79K/mo

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 2 days ago

New


AdventHealth rating

7.4

Company rating: 7.4 out of 10

Based on 1,276 frontline employees who took The Breakroom Quiz

269th of 889 rated healthcare providers


Job description

Our promise to you:

Joining AdventHealth is about being part of something bigger. It’s about belonging to a community that believes in the wholeness of each person, and serves to uplift others in body, mind and spirit. AdventHealth is a place where you can thrive professionally, and grow spiritually, by Extending the Healing Ministry of Christ. Where you will be valued for who you are and the unique experiences you bring to our purpose-minded team. All while understanding that together we are even better.

All the benefits and perks you need for you and your family:

  • Benefits from Day One: Medical, Dental, Vision Insurance, Life Insurance, Disability Insurance

  • Paid Time Off from Day One

  • 403-B Retirement Plan

  • 4 Weeks 100% Paid Parental Leave

  • Career Development

  • Whole Person Well-being Resources

  • Mental Health Resources and Support

  • Pet Benefits

Schedule:

Full time

Shift:

Day (United States of America)

Address:

1035 RED BUD RD NE

City:

CALHOUN

State:

Georgia

Postal Code:

30701

Job Description:

Work Schedule: Monday - Friday, no call no weekends.

  • Manages end-to-end clinical research activities, including patient screening, eligibility, enrollment, and follow-up care.
  • Serves as the primary liaison for participants, investigators, and internal/external research partners.
  • Ensures compliance with clinical research standards, protocols, and AHRI procedures across all patient-facing activities.
  • Coordinates biospecimen collection and maintains HIPAA-compliant databases linking patient data to research samples.
  • Supports research operations through data collection, chart review, and collaboration with clinical, lab, and regulatory teams.

Knowledge, Skills, and Abilities:
• Ability to work independently in a fast-paced clinical or research environment, handling multiple tasks simultaneously, effectively, and in an organized and timely manner. [Required]
• Knowledge of HIPAA data protection and patient advocacy or similar awareness of ethical treatment of participants in research. [Required]
• Ability to communicate effectively with research participants, investigators, research staff, and external partners. [Required]
• Ability to apply an analytical approach to problem solving, obtain and analyze facts, and apply sound judgement. [Required]
• Ability to accept direction and respond to the changing needs of clinical research units. [Required]
• Working knowledge of Microsoft Office applications, such as Word, Excel, Access, Outlook, and Internet knowledge and skills. [Required]
• Proficient in the ability to navigate through various electronic data transfer portals and systems. [Required]
• Excellent organizational, multi-tasking, and problem-solving skills with extreme attention to detail. [Required]
• Strong interpersonal skills to interact and maintain good relationships with a broad spectrum of healthcare disciplines and the public. [Required]
• Excellent understanding of project management concepts in order to ensure protocol compliance. [Required]
• Specialized knowledge of the unique needs of patients in the assigned therapeutic areas undergoing treatment. [Required]
• One to two years skill in human life sciences/biomedical research; physiological, cellular, biochemical, or molecular biology. [Required]
• Clinical Trials Management System (or equivalent) and/or Electronic Data Capture (EDC) exposure. [Required]
• Advanced computer skills. [Required]
• Knowledge of clinical research and research regulatory environment. [Required]
Education:
• Bachelors [Required]
• Master's [Preferred]
Field of Study:
• in a health related
Work Experience:
• 2+ years of direct clinical research experience or administrative/professional experience working with data or medical information to include duties such as data collection, management and verification [Preferred]
• Healthcare experience (medical assistant, allied health care professional, etc.) within an office or hospital setting. [Preferred]
Additional Information:
• An equivalent combination of education and relevant work experience may be considered in lieu of the stated degree requirement:

- Bachelor’s degree in healthcare or related field AND 0+ research experience OR
- Bachelor’s degree in any field AND research experience OR
- Associate’s degree in healthcare or related field AND 2+ years of clinical research or healthcare experience OR
- Graduate of an accredited allied health certificate program AND 4+ years of clinical research or healthcare experience
• Other certification as applicable to clinical degree or program (i.e., medical assistant, medical technician, phlebotomy) [Preferred]
Licenses and Certifications:
• Certified Clinical Research Coordinator (CCRC) [Required] OR Certified Clinical Research Professional (SOCRA) (CCRP) [Required] 
• Basic Life Support - CPR Cert (BLS) [Preferred]

Pay Range:

$42,839.79 - $79,674.53

This facility is an equal opportunity employer and complies with federal, state and local anti-discrimination laws, regulations and ordinances.


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