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Clinical Risk Management Jobs in Atlanta, GA (NOW HIRING)

Peachtree Behavioral LLC

Clinical Therapist

Atlanta, GA · On-site

$56K - $76K/yr

Collaborates with Clinical Director for risk management. * Establish positive and cooperative relationships with local health care entities and vendors. * Attend staff meetings, supervisory ...

ConvaTec

Clinical Strategy Lead

Atlanta, GA · On-site +1

... risk management, and other activities as needed. * Act as a subject matter expert in the product ... Clinical background (MD, RN, DPM, DNP, or similar) r equired * Specialty knowledge in wound care ...

CONVATEC GROUP PLC

Clinical Strategy Lead

Atlanta, GA · On-site +1

... risk management, and other activities as needed. * Act as a subject matter expert in the product ... Clinical background (MD, RN, DPM, DNP, or similar) r equired * Specialty knowledge in wound care ...

Werfenlife SA.

Senior Quality Engineer

Norcross, GA · On-site

$83K - $113K/yr

Collaborate at a systems level with R&D, Clinical, and other functions to identify risks, implement risk controls, and maintain a living risk management file. * Review design and process changes ...

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Clinical Risk Management information

See Atlanta, GA salary details

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How much do clinical risk management jobs pay per hour?

As of Sep 15, 2026, the average hourly pay for clinical risk management in Atlanta, GA is $33.29, according to ZipRecruiter salary data. Most workers in this role earn between $15.96 and $31.68 per hour, depending on experience, location, and employer.

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

Professionals in Clinical Risk Management often encounter challenges such as staying current with complex healthcare regulations, effectively communicating risks to diverse clinical teams, and managing competing priorities under tight deadlines. Navigating these challenges requires strong analytical skills, continuous education on regulatory updates, and fostering a culture of open communication within the organization. Collaborating closely with clinicians, administrators, and legal teams ensures that risk mitigation strategies are practical and effectively implemented.

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

To thrive as a Clinical Risk Manager, you need expertise in healthcare regulations, risk assessment, patient safety, and a relevant degree such as nursing, healthcare administration, or risk management. Familiarity with incident reporting systems, data analysis tools, and certification such as CPHRM (Certified Professional in Healthcare Risk Management) are commonly required. Excellent problem-solving, communication, and negotiation skills help facilitate effective collaboration across multidisciplinary teams. These skills are vital for identifying potential risks, implementing preventive strategies, and ensuring regulatory compliance to enhance patient safety and organizational performance.

What is the difference between Clinical Risk Management vs Clinical Risk Coordinator?

AspectClinical Risk ManagementClinical Risk Coordinator
CertificationsCertifications in risk management, healthcare complianceOften similar certifications, focus on coordination
Work EnvironmentStrategic, policy development, oversight rolesOperational, day-to-day risk monitoring and reporting
Employer & Industry UsageHospitals, healthcare organizations, insurance companiesHospitals, clinics, healthcare facilities

Clinical Risk Management involves developing policies and strategies to minimize risks across healthcare settings, focusing on compliance and overall risk reduction. In contrast, a Clinical Risk Coordinator handles the implementation of risk mitigation plans, monitors incidents, and reports on risk issues. Both roles require healthcare knowledge and risk-related certifications but differ in scope and strategic versus operational focus.

Is healthcare risk management a good career?

Healthcare risk management is a growing field that involves identifying and reducing risks to improve patient safety and compliance. It typically requires knowledge of healthcare regulations, strong analytical skills, and certifications such as Certified Professional in Healthcare Risk Management (CPHRM). The role offers stability and opportunities for advancement in healthcare organizations.

What do clinical risk managers do?

Clinical risk managers identify, assess, and develop strategies to reduce risks related to patient safety and healthcare quality. They analyze incident reports, implement safety protocols, and ensure compliance with healthcare regulations, often using data analysis tools. Their role helps prevent medical errors and improve overall patient care outcomes.

What does clinical risk management mean?

Clinical risk management is a key responsibility for professionals in healthcare roles, including clinical risk managers. It involves identifying, assessing, and mitigating risks to patient safety and care quality through policies, procedures, and data analysis. This process helps prevent adverse events and ensures compliance with healthcare regulations.
Clinical Risk Management jobs near you
Infographic showing various Clinical Risk Management job openings in Atlanta, GA as of September 2026, with employment types broken down into 83% Full Time, and 17% Contract. Highlights an 66% In-person, 17% Hybrid, and 17% Remote job distribution, with an average salary of $69,242 per year, or $33.3 per hour.

Sr. Project Manager, Clinical Research

Kennesaw, GA • On-site

Artivion
Biotechnology Research and Development • 1 - 5K employees
Learn more about Artivionexternal

Full-time

Posted 4 days ago

Artivion rating

8.7

Company rating: 8.7 out of 10

Based on 6 frontline employees who took The Breakroom Quiz

Job description

Company Overview:

Headquartered in suburban Atlanta, Georgia, Artivion, Inc. is a medical device company focused on developing simple, elegant solutions that address cardiac and vascular surgeons’ most difficult challenges in treating patients with aortic diseases. Artivion has over 1,600 employees worldwide with sales representation in over 100 countries. The Company has manufacturing facilities located in Atlanta, Georgia, Austin, Texas and Hechingen, Germany. Additionally, it has sales and distribution offices in various countries throughout Europe, Asia, and South America. For additional information about Artivion, visit our website, www.artivion.com. 

Overview:

This role independently leads the execution and management of clinical studies from study design and start-up through completion, serving as a key point of contact for internal teams, study sites, vendors, and other clinical partners.

Responsibilities:

  • Collaborates on clinical study design with goal to serve as subject matter expert (SME).
  • Responsible for the development of all clinical documents including but not limited to the clinical study protocol, case report forms, informed consent forms, clinical study agreements, investigator manuals, investigator files, and all other necessary documentation for study initiation (the development of several clinical documents falls under the responsibility of other clinical functions in the EU).
  • Independently responsible for all clinical study activities including but not limited to primary contact for internal/external clinical customers (such as Monitor, Data Manager, clinical study sites, etc.), leads clinical study team meetings, establishes and manages the study timeline, anticipating schedule impacts and adjusting project team activities where required.
  • Facilitates completion of regulatory submissions and drafts written submissions/responses for regulatory bodies as needed.
  • Ensures the project team maintains a continuous state of audit readiness
  • Aware of Institutional Review Board (IRB) / Ethic Committee (EC) reporting requirements.
  • Establishes plans for escalation and/or field assurance issues; assesses key protocol-specific parameters and escalates as appropriate.
  • May participate on a cross-functional core team.
  • Collaborates with Quality and other Risk Management stakeholders contributing to the proactive identification, assessment, and management of clinical study risks.
  • Acts as a point of contact for vendors including but not limited to managing the vendor selection process, review/initiate the vendor contract and payments.
  • Establishes and manages the clinical study budget, collaborating impacts/risks to timeline and budget; may work directly with Finance partners.
  • Responsible for site management including but not limited to site qualification, initiation, and non-compliances.
  • Independently submits clinical studies to ethical boards when needed.
  • Responsible for developing trainings and ensuring team members are trained (responsible for developing all trainings and training of all team members in the US).
  • May deliver Health Care Provider (HCP) presentations.
  • Creates cross functional collaboration workflows to support milestones.
  • May verify, review, and track CRFs.
  • Ensures that centralized data reviews are conducted and is involved in query resolution with the site, where required.
  • Collaborates on clinical study reports based on study management and/or tracking needs.
  • Liaisons with the Statistician.
  • Ability to travel domestically and internationally up to 30% of the time.

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