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Weekend Clinical Research Regulatory Jobs in Decatur, GA

Alcanza Clinical Research

Clinical Research Coordinator

Decatur, GA · On-site

$23.75 - $31.50/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

The Clinical Research Coordinator (CRC) works to ensure the execution of assigned studies in compliance with GCP, ICH, HIPAA, FDA Regulations and SOPs. Key Responsibilities Essential Job Duties: In ...

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Weekend Clinical Research Regulatory information

See Decatur, GA salary details

$17

$43

$61

How much do weekend clinical research regulatory jobs pay per hour?

As of Aug 18, 2026, the average hourly pay for weekend clinical research regulatory in Decatur, GA is $43.09, according to ZipRecruiter salary data. Most workers in this role earn between $35.43 and $51.15 per hour, depending on experience, location, and employer.

What is a Weekend Clinical Research Regulatory professional?

A Weekend Clinical Research Regulatory professional is responsible for ensuring that clinical research studies comply with all regulatory requirements, specifically during weekend shifts. Their duties include preparing and submitting regulatory documents, maintaining ethical standards, and communicating with regulatory agencies and institutional review boards. They play a crucial role in supporting research teams by facilitating timely approvals and monitoring compliance, allowing research activities to continue smoothly over the weekend.

What are the key skills and qualifications needed to thrive as a Weekend Clinical Research Regulatory professional?

To thrive as a Weekend Clinical Research Regulatory professional, you need a solid understanding of clinical research protocols, regulatory guidelines (such as FDA and ICH-GCP), and often a degree in life sciences or a related field. Familiarity with electronic regulatory systems, IRB submission platforms, and certification like CCRC or ACRP is typically required. Excellent attention to detail, strong organizational skills, and effective written communication make someone stand out in this position. These skills ensure that all research activities comply with regulations, maintain data integrity, and support the smooth operation of clinical trials.

What are some common challenges faced by Weekend Clinical Research Regulatory professionals, and how can they be managed?

Weekend Clinical Research Regulatory professionals often face challenges related to limited access to stakeholders and timely responses, as many team members and institutional review boards may not be available outside standard business hours. Managing regulatory documents and ensuring compliance within tight weekend deadlines can also be demanding. Effective planning, clear communication with the weekday team, and utilizing digital tools for document management can help overcome these hurdles. Building strong relationships with colleagues and maintaining detailed handover notes are essential strategies for success in this role.

What is the difference between Weekend Clinical Research Regulatory vs Weekend Clinical Research Coordinator?

AspectWeekend Clinical Research RegulatoryWeekend Clinical Research Coordinator
CertificationsRegulatory Affairs Certification (RAC), Clinical Research CertificationsCPR, Clinical Research Certification
Work EnvironmentRegulatory agencies, compliance departments, sponsor officesResearch sites, hospitals, clinics
Job FocusEnsuring regulatory compliance, preparing submissionsParticipant recruitment, data collection, site coordination

Weekend Clinical Research Regulatory professionals focus on regulatory compliance and submissions, working mainly in offices or regulatory agencies. In contrast, Weekend Clinical Research Coordinators handle participant interactions and data collection at research sites. Both roles require clinical research certifications but differ in daily tasks and work settings.

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

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

Weekend Clinical Research Regulatory jobs near you

Regulatory Affairs Specialist (North America)

Alimentiv

Atlanta, GA • Remote

Full-time

Re-posted 6 days ago

Job description

Responsible for the day-to-day activities and delivery of Global Regulatory Affairs support services. Role will include management of clinical trial applications to Competent Authorities, Ethics Committees and Regulatory Agencies, and the research, review and reporting on applicable global regulations and requirements. Develop stakeholder tools, process/document regulatory risk assessments, and provide support, expertise and represent the unit with other functional units, sponsors, researchers and/or regulatory authorities.  Ensure high quality, timely service delivery processes are maintained in accordance with corporate, industry and regulatory standards and guidelines.  May be required to coach peers and/or provide input for staff performance reviews. 
Unit Management
  • Coordinate the day to day delivery of regulatory services and processes, including compilation of regulatory filings/submissions/revisions for projects, third party vendors and clinical sites.
  • Conduct or assist with regulatory and/or safety reviews, create regulatory-related tools, educational/training materials, and remain current on all aspects of clinical research regulatory requirements and industry best practices, communicating changes to project leaders in a timely manner.
Client Services
  • As the corporate subject specialist in regulatory affairs, provide regulatory, ethics and/or pharmacovigilance guidance and support to project stakeholders.
  • Represent the unit at project meetings, assisting with project education/regulatory tool development, at regulatory reviews and audits, with clients ensuring expectations are managed and met, with regulatory, ethics and government representatives and, when appropriate, respond to regulatory queries on behalf of the client.
Regulatory Strategy Development
  • Identify changes in clinical research regulatory requirements and industry best practices and recommend, implement, and maintain corporate regulatory strategies, working with other experts (safety, quality assurance) when appropriate, to meet or exceed compliance requirements of evolving regulatory initiatives.
  • Participate in specialized conferences/meetings to increase knowledge as needed.
Project Support
  • Regularly respond to registration requests and work with project teams to identify regulatory requirements.
  • Assist in the preparation of regulatory submissions and support summaries.
  • Ensure project/clinical site files and documents are developed, maintained, revised, archived and/or destroyed in accordance with project and regulatory requirements and that all project stakeholders are fully informed and trained on all applicable regulatory requirements.
Qualifications
  • Applicants should have a minimum of an undergraduate degree and 4-6 years of relevant experience in Clinical Research/Regulatory Affairs.
  • The successful candidate will possess strong knowledge of LATAM clinical trial regulations.
  • Fluency in English and Spanish (written and verbal) required.
Working Conditions
  • Home-based
  • *Accommodations for job applicants with disabilities are available upon request.
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
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