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Remote Clinical Research Regulatory Jobs in Decatur, GA

ICON

Senior Clinical Research Associate

Atlanta, GA · On-site +1

Senior Clinical Research Associate - Cardio (Smartpulse A-fib) - All Regions ICON is a global ... In-depth knowledge of FDA regulations and ICH/GCP guidelines. * Strong problem-solving skills to ...

Danaher

Principal Clinical Scientist

Atlanta, GA · On-site +1

... remote based (can also be onsite in Chaska, MN). At Danaher Diagnostics, our vision is to be the ... Partner crossfunctionally with R&D, Regulatory, Medical Affairs, Quality, and Commercial teams to ...

New

IQVIA

Clinical Trial Rater

Atlanta, GA · Remote

... and regulatory requirements. This role requires strong clinical judgment, experience with ... Flexible, remote work schedule. * Opportunity to contribute to global clinical research.

IQVIA

Clinical Project Lead, Oncology

Atlanta, GA · Remote

$68K - $232K/yr

In this remote role you will serve as the primary country-level leader for clinical trial delivery ... Coordinate ethics and regulatory submissions/approvals in collaboration with start-up teams

YO AI Labs

Biostatistician Expert - Remote

Atlanta, GA · Remote

$60 - $70/hr

Review Clinical Study Reports (CSRs) and regulatory submission data. * Perform statistical analyses ... Research). * MSc or PhD in Biostatistics, Statistics, or a related field. * Experience with ...

LivaNova

Regulatory & Clinical Specialist

Atlanta, GA · Remote

$85K - $95K/yr

The Regulatory and Clinical Specialist will support the clinical evaluation activities, review ... This is a remote role (candidates must be based in the United States) * Occasional travel may be ...

YO AI Labs

Regulatory Affairs Expert - Remote

Atlanta, GA · Remote

$50 - $80/hr

Remote Job Type: Contract We are seeking an experienced Regulatory Affairs Specialist to support AI ... The role involves assessing clinical documents, ensuring compliance with regulatory guidelines ...

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Remote Clinical Research Regulatory information

See Decatur, GA salary details

$47.8K

$104.8K

$184.5K

How much do remote clinical research regulatory jobs pay per year?

As of Aug 27, 2026, the average yearly pay for remote clinical research regulatory in Decatur, GA is $104,796.00, according to ZipRecruiter salary data. Most workers in this role earn between $79,100.00 and $119,600.00 per year, depending on experience, location, and employer.

What is a remote clinical research regulatory professional?

A Remote Clinical Research Regulatory professional is responsible for ensuring that clinical research studies comply with all regulatory requirements while working remotely. This role involves preparing and submitting regulatory documents, maintaining compliance with federal and international guidelines, and communicating with regulatory agencies. Professionals in this field support research teams by guiding them through the approval processes required for clinical trials. Their work is essential for protecting study participants and ensuring the integrity of research data.

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

To thrive as a Remote Clinical Research Regulatory professional, you need a solid understanding of clinical research protocols, regulatory compliance, and relevant guidelines such as GCP, often supported by a bachelor's degree in life sciences or a related field. Familiarity with regulatory submission platforms (like IRB management systems), eTMF systems, and certifications such as SOCRA or ACRP are typically required. Strong organizational skills, attention to detail, and effective remote communication make candidates stand out in this role. These competencies ensure regulatory accuracy, maintain study integrity, and foster efficient collaboration across geographically dispersed teams.

What are some common challenges faced by remote clinical research regulatory professionals, and how can they be managed effectively?

Remote clinical research regulatory professionals often face challenges such as coordinating with cross-functional teams across different locations, managing time zone differences, and ensuring timely submission of regulatory documents. Effective communication skills and proficiency with digital collaboration tools are essential to stay organized and maintain compliance. Regular virtual meetings, clear documentation practices, and robust project management systems can help mitigate these challenges and ensure smooth regulatory processes.

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

AspectRemote Clinical Research RegulatoryRemote Clinical Research Coordinator
Required CredentialsRegulatory certifications, life sciences degreeResearch experience, clinical trial knowledge
Work EnvironmentRegulatory agencies, sponsor offices, remote documentation reviewClinical sites, data collection, participant coordination
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsResearch sites, hospitals, research organizations
Common Search & ComparisonRegulatory compliance, documentation, submissionsParticipant management, trial coordination

Remote Clinical Research Regulatory professionals focus on ensuring compliance with regulations, preparing submissions, and managing documentation remotely. In contrast, Remote Clinical Research Coordinators handle participant recruitment, data collection, and trial logistics. Both roles are essential in clinical research but differ in their focus and responsibilities.

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:

What job categories do people searching Remote Clinical Research Regulatory jobs in Decatur, GA look for?

The top searched job categories for Remote Clinical Research Regulatory jobs in Decatur, GA are:

What cities near Decatur, GA are hiring for Remote Clinical Research Regulatory jobs?

Cities near Decatur, GA with the most Remote Clinical Research Regulatory job openings:

Remote Clinical Research Regulatory jobs near you

Senior Clinical Research Associate - US

Atlanta, GA • On-site, Remote

Optimapharm d.o.o.
See more jobs at Optimapharm d.o.o.external

Full-time

Medical, Dental, Vision, Retirement, PTO

This job post has expired 1 day ago. Applications are no longer accepted.

Job description

Location: Remote
Who we are?
Optimapharm is a mid-sized, global Contract Research Organisation (CRO) turning science into hope through agile, patient-focused clinical development. We specialise in Phase I-IV clinical studies, delivering Full-Service and Functional Service Provision (FSP) solutions that help sponsors move faster and execute with confidence.
With operations in 40+ countries and 2x the patient reach of the average mid-sized CRO, we enable accelerated regulatory pathways, faster study start-up, and access to diverse patient populations worldwide. At Optimapharm, you'll contribute to meaningful clinical research while growing your career in a dynamic, people‑focused, global environment.
As our US Clinical Operations team continues to grow, we're looking for a Senior CRA who is committed to clinical excellence, passionate about mentoring others, and driven by the opportunity to help bring innovative treatments to patients faster.
At Optimapharm, you'll work on diverse and challenging studies, collaborate with experienced professionals around the world, and play a critical role in shaping the success of clinical trials - all within a culture that supports continuous growth and recognizes expertise.
What do we offer?
  • Working in a successful company that's growing and developing every day
  • Being part of a clinical research team that transforms science into hope for patients
  • International projects and professional growth
  • Company that supports life balance
  • Company with healthy culture
  • Working with a highly experienced team of clinical research professionals
  • Competitive salary
  • Competitive PTO entitlement
  • Health insurance, including vision and dental plans, to meet your and your family's needs
  • Comprehensive pension plan to maximize savings and prepare confidently for the future
  • Employee engagement programs
  • Well-being initiatives
  • Training and development program
  • Fast-paced career path progression

Who are we looking for?
Qualifications and Experience
  • University degree, preferably in medical or life sciences; nursing education or other relevant healthcare college degree
  • At least 3-5 years of independent clinical trial monitoring experience in oncology
  • High level of knowledge of ICH GCP Guidelines, knowledge of regulatory requirements and a strong interest in clinical research
  • Computer proficiency is mandatory
  • Ability to read, analyze, and interpret common scientific and technical journals
  • Excellent verbal and written communication skills
  • Very good interpersonal and negotiation skills
  • Ability to work independently, pro-active
  • Affinity to work effectively and efficiently in a matrix environment
  • A current, valid driver's license

Your responsibilities
  • Perform routine site visits independently, including pre-study, initiation, interim monitoring and closeout visits
  • Manage assigned sites by regular contact with site personnel to ensure site compliance, adequate enrolment and understanding of study requirements
  • Independently perform CRF review; query generation and resolution against established data review guidelines or data management systems as applicable
  • Identifying and escalating potential risks and identifying retraining opportunities for site personnel
  • Preparation of corrective and preventive (CAPA) plans for issues identified during monitoring activities and pro-active follow of each, individual CAPA until timely resolution
  • Preparation of documents required for EC submissions and notifications, translation of study-related documents (where applicable), and other tasks as instructed by the supervisor
  • Independently negotiate study budgets with potential investigators/institutions and assist with the execution of site contracts as applicable
  • Administration of site payments in accordance with relevant project instructions

By joining our fast-growing and prosperous team, you will have an excellent opportunity for further personal growth and career development.
If you would be interested in joining the Optimapharm team, please send your CV and note that only shortlisted candidates who meet the requirements will be contacted for the further selection process.
Compensation is competitive and final offers will reflect each candidate's experience, skills, and qualifications.
Disclaimer: Unsolicited CVs sent to Optimapharm (Talent Acquisition Team, Hiring Managers or any other OPT employee) by recruitment agencies will not be considered for this role. Optimapharm follows a direct sourcing strategy and collaborates exclusively with selected recruitment partners when external support is required.

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