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Cra Assistant Jobs in Atlanta, GA (NOW HIRING)

Hope Bank

Portfolio Officer - CBG

Duluth, GA

$85K - $90K/yr

... manager. * Assist in loan closing and funding including obtaining signatures on loan documents ... Reg B, HMDA, Bank Secrecy Act, OFAC, and USA Patriot Act, CRA, Privacy, and Security. * Comply with ...

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Cra Assistant information

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How much do cra assistant jobs pay per hour?

As of Aug 27, 2026, the average hourly pay for cra assistant in Atlanta, GA is $33.44, according to ZipRecruiter salary data. Most workers in this role earn between $17.13 and $46.64 per hour, depending on experience, location, and employer.

What is a CRA Assistant?

A Clinical Research Associate (CRA) Assistant supports clinical trials by managing documents, coordinating meetings, and assisting with regulatory compliance. They help ensure studies follow protocols and regulatory requirements. CRA Assistants often handle administrative tasks, maintain trial records, and communicate with clinical sites. Their role is essential in supporting CRAs and ensuring the smooth operation of clinical research processes.

What are the main responsibilities of a CRA Assistant?

As a CRA Assistant, your primary responsibilities include supporting clinical research associates with administrative tasks such as organizing trial documentation, maintaining study files, scheduling site visits, and tracking regulatory submissions. You may also assist in preparing reports, following up with clinical sites, and ensuring data accuracy and proper documentation. The role often involves close collaboration with other team members, including project managers, study coordinators, and regulatory staff. This supportive position is critical for maintaining smooth trial operations and provides valuable hands-on experience for those interested in advancing within clinical research.

What are the key skills and qualifications needed to thrive in the CRA Assistant position, and why are they important?

To thrive as a CRA Assistant, you need a solid understanding of clinical research processes, attention to detail, and a background in life sciences or healthcare. Experience with electronic data capture (EDC) systems, Microsoft Office Suite, and knowledge of Good Clinical Practice (GCP) guidelines or certifications are often required. Excellent organizational skills, proactive communication, and the ability to manage multiple tasks make candidates stand out. These attributes are vital to support clinical research associates (CRAs), ensure regulatory compliance, and facilitate smooth clinical trial operations.

Is it hard to get a CRA assistant job?

Getting a CRA assistant job can be competitive, often requiring relevant education such as a degree in life sciences or related fields, along with strong organizational and communication skills. Prior experience or knowledge of clinical trial processes and familiarity with regulatory guidelines can improve chances of hiring. Entry-level positions may have less strict requirements, but overall, securing the role involves demonstrating attention to detail and understanding of clinical research environments.

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

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Cra Assistant jobs near you
Infographic showing various Cra Assistant job openings in Atlanta, GA as of August 2026, with employment types broken down into 50% Full Time, and 50% Part Time. Highlights an 100% In-person job distribution, with an average salary of $69,553 per year, or $33.4 per hour.

Clinical Research Associate (CRA) -Cardiovascular Medical Device

Marietta, GA • On-site

Mirus LLC
1 - 10 employees
Learn more about Mirus LLCexternal

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 7 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%

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