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Clinical Study Manager Jobs in Atlanta, GA (NOW HIRING)

Denali Health

Clinical Research Coordinator III

Atlanta, GA · On-site

$23.25 - $31/hr

Denali Health is a fast-growing clinical research organization dedicated to improving patient ... Study Management: * Ensure that study activities are conducted in accordance with GCP, IRB ...

Actalent

Clinical Research Coordinator

Atlanta, GA · On-site

$22 - $25/hr

Use tablets and other study-related technology to collect and manage data during study visits ... Clinical research experience, including at least one year in a clinical research setting; academic ...

Socket.dev

Key Accounts Director (New York)

Atlanta, GA · On-site

$205 - $240/hr

HARMONi: Phase 3 clinical study which was intended to evaluate ivonescimab combined with ... Manage relationships and identify opportunities with select access stakeholders (e.g., NCODA, COA ...

Artivion

Sr. Clinical Data Manager

Kennesaw, GA · On-site

This also includes data support for department projects, and inquiries, unrelated to clinical studies. Responsibilities: * Lead, manage, execute end-to-end data management activities for clinical ...

MMS

Senior Medical Writer (Remote)

Atlanta, GA · On-site

Substantial clinical study protocol experience, as lead author, required * Experience leading and managing teams while authoring regulatory documents with aggressive timelines * Experience in ...

CryoLife

Sr. Clinical Data Manager

Kennesaw, GA · On-site

This also includes data support for department projects, and inquiries, unrelated to clinical studies. Responsibilities: * Lead, manage, execute end-to-end data management activities for clinical ...

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Clinical Study Manager information

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How much do clinical study manager jobs pay per hour?

As of Sep 3, 2026, the average hourly pay for clinical study manager in Atlanta, GA is $60.83, according to ZipRecruiter salary data. Most workers in this role earn between $49.38 and $68.56 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a clinical study manager?

To thrive as a Clinical Study Manager, you need a strong background in clinical research, project management, and regulatory compliance, typically supported by a degree in life sciences and experience in clinical trials. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and certifications like GCP (Good Clinical Practice) are highly valued. Strong organizational, leadership, and communication skills help manage cross-functional teams and ensure study timelines are met. These skills are crucial for maintaining study quality, ensuring regulatory adherence, and delivering successful trial outcomes.

What are some common challenges faced by clinical study managers, and how can they be addressed?

Clinical Study Managers often encounter challenges such as coordinating multiple stakeholders, ensuring regulatory compliance, and managing tight timelines across study sites. Effective communication and proactive planning are essential to address these issues, as well as staying up to date with changing industry regulations. Building strong relationships with site staff and fostering a collaborative team environment can also help mitigate delays and ensure study milestones are met successfully.

How much does a clinical study manager earn?

A clinical study manager's salary varies based on experience, location, and the size of the organization, but typically ranges from $80,000 to $130,000 annually. Senior roles or those with specialized skills and certifications can earn higher salaries, often exceeding $150,000. The position often requires knowledge of regulatory guidelines and project management tools.

What does a clinical study manager do?

A clinical study manager oversees the planning, execution, and monitoring of clinical trials to ensure they comply with regulatory standards and protocols. They coordinate with research teams, manage timelines and budgets, and ensure data quality, often using specialized software and requiring knowledge of Good Clinical Practice (GCP) guidelines.

What are the most commonly searched types of Clinical Study jobs in Atlanta, GA?

The most popular types of Clinical Study jobs in Atlanta, GA are:

What are popular job titles related to Clinical Study Manager jobs in Atlanta, GA?

For Clinical Study Manager jobs in Atlanta, GA, the most frequently searched job titles are:

What job categories do people searching Clinical Study Manager jobs in Atlanta, GA look for?

The top searched job categories for Clinical Study Manager jobs in Atlanta, GA are:

What cities near Atlanta, GA are hiring for Clinical Study Manager jobs?

Cities near Atlanta, GA with the most Clinical Study Manager job openings:

Clinical Study Manager jobs near you
Infographic showing various Clinical Study Manager job openings in Atlanta, GA as of August 2026, with employment types broken down into 86% Full Time, 11% Part Time, and 3% Contract. Highlights an 83% Physical, 2% Hybrid, and 15% Remote job distribution, with an average salary of $126,532 per year, or $60.8 per hour.

Clinical Research Associate (CRA) -Cardiovascular Medical Device

Mirus LLC

Marietta, GA • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 15 days ago

Job description


Role: Clinical Research Associate (CRA) - Cardiovascular Medical Device 

Location: Remote  

Position Summary: 

Assist with the management of cardiovascular clinical studies for MiRus products with a focus on adherence to critical timelines, high-caliber document development and quality data collection. The applicant should possess strong critical thinking skills and the ability to comprehend technical subject matter to effectively contribute to the organization.

Essential Duties and Responsibilities:
 

  • Contribute to content generation, writing and editing of study protocols, amendments, informed consents, committee charters, study reports, monitoring plans, and other related clinical and regulatory documents.
  • Assist with the management of investigational studies from start through study closure.
  • Engage in new study trial design with cross functional teams, including clinical and pre-clinical research and development groups.
  • Contribute to the development of CRFs
  • Assist with the formulation of instructional materials and training of investigators, study coordinators and associated study site personnel on the conduct of the clinical trials, as applicable.
  • Assist Study Manager with safety monitoring including preparing supporting documentation for CEC and/or DSMB, meetings, agenda, data review, presentations, and updating relevant trackers as applicable.
  • Serve as a point of contact between clinical site investigators and the MiRus team.
  • Work with investigators and site personnel to quickly and effectively resolve discrepancies.
  • May be responsible for patient accruals and tracking payments to sites for clinical study programs
  • Serve as a point of contact between CRO personnel and MiRus.
  • Oversee/support CRO and field study monitors, with monitoring related items and follow-up on study tasks.
  • Monitor ongoing compliance to study protocols in accordance with applicable regulations and GCP, work instructions, guidelines and/or policies.
  • Provide continuous data review of source documents, case report forms, data reports as appropriate.
  • Assist in review of monitoring reports and tracking of action items.
  • Review source documentation to confirm subject eligibility for clinical trials.
  • Track and upload study imaging
  • Manage clinical study documentation (trial master file and study related tracking).
  • Update and design as needed study dashboards, study trackers and other applicable study documents to provide regular updates on trial status to Study Manager
  • Interact with data management, as applicable
  • Support applications and technical files as needed.
  • Assist with preparation for investigators meetings.

 Minimum Education and/or Experience: 

  • Bachelor’s or Master’s degree in nursing with clinical experience in the cardiac field (CCU, CVOR, Cath Lab) and experience in a clinical research role.  CRA certification desired.
  • At least 2 years of experience in clinical research role, with at least 2 years in CRA role, preferably in cardiovascular medical device.
  • Experience in clinical trials and/or post-market registries in the U.S., Australian and/or European Union, with other geographies desired.
  • Current knowledge of medical device clinical trials design and best practices.
  • Proficient knowledge of FDA regulations and ICH/GCP guidelines, guidance documents, and other applicable regulations and standards, and implementation of these standards in the medical device industry, in the U.S. and all countries in which trials are conducted.
  • General application of medical terminology (cardiovascular specific preferred).

 Benefits:
MiRus offers competitive compensation, options, full benefits, and relocation assistance.

  •  401(k)
  •  Dental insurance
  • Vision insurance
  •  Disability insurance
  •  Employee assistance program
  •  Flexible spending account or Health Savings Account
  •  Health insurance
  •  Life insurance
  •  Paid time off

 Schedule:

  • Monday to Friday (8am – 5pm)

Work Location:

  • Remote
  • Position may require domestic travel at least 20-40%