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Remote Clinical Trial Manager Jobs in Decatur, GA

Biostatistician

South Fulton, GA ยท Remote

$60 - $100/hr

Remote micro1 is engaging Biostatisticians to contribute to a customer's advanced project in AI ... clinical trial analysis, regulatory submission reviews, and observational study assessments.

Biostatistician

Sandy Springs, GA ยท Remote

$60 - $100/hr

Remote micro1 is engaging Biostatisticians to contribute to a customer's advanced project in AI ... clinical trial analysis, regulatory submission reviews, and observational study assessments.

Remote micro1 is engaging Biostatisticians to contribute to a customer's advanced project in AI ... clinical trial analysis, regulatory submission reviews, and observational study assessments.

Director of Biostatistics

Atlanta, GA ยท Remote

$60 - $100/hr

Remote micro1 is engaging Biostatisticians to contribute to a customer's advanced project in AI ... clinical trial analysis, regulatory submission reviews, and observational study assessments.

Remote micro1 is engaging Biostatisticians to contribute to a customer's advanced project in AI ... clinical trial analysis, regulatory submission reviews, and observational study assessments.

Biostatistician

Atlanta, GA ยท Remote

$60 - $100/hr

Remote micro1 is engaging Biostatisticians to contribute to a customer's advanced project in AI ... clinical trial analysis, regulatory submission reviews, and observational study assessments.

Showing results 21-40

Remote Clinical Trial Manager information

See Decatur, GA salary details

$28

$61

$93

How much do remote clinical trial manager jobs pay per hour?

As of Aug 21, 2026, the average hourly pay for remote clinical trial manager in Decatur, GA is $61.04, according to ZipRecruiter salary data. Most workers in this role earn between $49.52 and $68.75 per hour, depending on experience, location, and employer.

What is a remote clinical trial manager?

A Remote Clinical Trial Manager is a professional responsible for overseeing the planning, execution, and management of clinical trials from a remote location. They coordinate with various teams, ensure regulatory compliance, monitor trial progress, and manage budgets and timelines, all while working off-site. This role typically involves using digital tools to communicate, track data, and ensure the trial runs smoothly and efficiently. Remote Clinical Trial Managers are essential in facilitating clinical research, especially in decentralized or multi-site studies. They play a key role in ensuring that clinical trials meet both scientific and regulatory standards.

What does a remote clinical trial manager do?

Remote clinical trial managers monitor the process of clinical testing from home or another location outside of the office or lab. In this role, you may collaborate with the clinical project manager to create outlines for the trial, research relevant information from existing medical studies, and help ensure the scope of the testing is enough to move the product forward to the next phase. Products may include pharmaceuticals, medical devices, or other forms of medical treatments. Your job duties also involve creating strategies for efficient testing methods, checking that all tests comply with safety standards and current government regulations, documenting results, and supervising research assistants.

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

To thrive as a Remote Clinical Trial Manager, you need expertise in clinical research, regulatory compliance, and project management, usually supported by a degree in life sciences and experience in clinical trials. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and GCP certification are typically required. Exceptional organizational skills, proactive communication, and the ability to lead cross-functional teams remotely set top performers apart. These competencies are crucial for ensuring trial integrity, regulatory adherence, and seamless coordination across distributed teams.

How does a remote clinical trial manager typically collaborate with on-site study teams and stakeholders?

As a Remote Clinical Trial Manager, you will frequently coordinate with on-site study teams, investigators, and sponsors through virtual meetings, project management platforms, and regular reporting. Effective communication and proactive problem-solving are essential for ensuring trial milestones are met and regulatory requirements are followed, despite not being physically present. You may also oversee remote monitoring visits, address site queries, and facilitate cross-functional collaboration between data management, safety, and regulatory teams. This structure allows for flexibility while maintaining strong oversight and quality standards.

What is the difference between Remote Clinical Trial Manager vs Remote Clinical Research Associate?

AspectRemote Clinical Trial ManagerRemote Clinical Research Associate
CredentialsTypically requires a Bachelor's or higher in life sciences, with experience in trial managementUsually holds a Bachelor's in life sciences or related field, with certification in clinical research (e.g., CCRP)
Work EnvironmentOversees multiple sites, manages trial timelines, budgets, and teams remotelyMonitors trial sites, ensures protocol compliance, and collects data remotely
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsPharmaceutical companies, CROs, clinical research organizations

The Remote Clinical Trial Manager focuses on overseeing entire clinical trials, managing teams, and ensuring project milestones are met. In contrast, the Remote Clinical Research Associate primarily monitors trial sites and data collection. Both roles require clinical research knowledge and often work remotely within the same industry sectors.

What are the most commonly searched types of Remote Clinical Trial jobs in Decatur, GA?

The most popular types of Remote Clinical Trial jobs in Decatur, GA are:

What are popular job titles related to Remote Clinical Trial Manager jobs in Decatur, GA?

For Remote Clinical Trial Manager jobs in Decatur, GA, the most frequently searched job titles are:

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

The top searched job categories for Remote Clinical Trial Manager jobs in Decatur, GA are:

What cities near Decatur, GA are hiring for Remote Clinical Trial Manager jobs?

Cities near Decatur, GA with the most Remote Clinical Trial Manager job openings:

Infographic showing various Remote Clinical Trial Manager job openings in Decatur, GA as of August 2026, with employment types broken down into 84% Full Time, 15% Part Time, and 1% Contract. Highlights an 81% Physical, 2% Hybrid, and 17% Remote job distribution, with an average salary of $126,957 per year, or $61 per hour.

$175K - $215K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 6 days ago


Job description

Description of Role

The MSL will serve as a field-based scientific expert responsible for engaging with healthcare professionals (HCPs), supporting clinical development, and ensuring alignment with Centessa's strategic medical objectives. This role is critical in translating complex scientific data into meaningful clinical insights and fostering compliant, evidence-based dialogue with thought leaders.

Key Responsibilities

Scientific Expertise & Thought Leader Engagement

  • Maintain a high level of therapeutic area expertise and scientific knowledge relevant to Centessa's pipeline and marketed products in alignment with Medical Affairs strategic objectives
  • Engage in compliant, non-promotional scientific exchange with key opinion leaders (KOLs), investigators, and other HCPs
  • Serve as a trusted scientific resource to external stakeholders, providing accurate and balanced medical information
  • Deliver company-approved, high-quality medical/scientific presentations to a variety of audiences including formulary committees and healthcare professionals.
  • Provide medical/scientific support for critical Centessa activities including speaker training, advisory boards, and sales training as appropriate
  • Ensure accurate, timely, and compliant documentation of field-based activities in accordance with MSL organization guidelines
    Clinical Trials Support
  • Collaborate with Clinical Operations to identify and evaluate potential clinical trial sites and investigators based on scientific expertise, patient population, and alignment with study objectives
  • Provide scientific education and protocol-specific training to investigators and site staff during site initiation visits, ensuring thorough understanding of study rationale and endpoints
  • Maintain ongoing engagement with trial sites and investigators to facilitate successful execution of clinical trial objectives, provide ongoing scientific support, address protocol-related inquiries, and ensure high-quality data generation
    Medical Conference Attendance & Coverage
  • Attend relevant scientific and medical congresses to stay current with emerging data and trends
  • Provide real-time insights and post-conference reports to internal teams
  • Support Centessa's presence at congresses through development of pre-conference plans, booth coverage, symposia attendance, and KOL engagement
  • Senior MSLs will be responsible for leading strategic conference planning, execution, and reporting
    Scientific Materials Development
  • Contribute to the development of scientific slide decks, FAQs, and educational materials
  • Writing and editing Medical Information response letters
  • Ensure all materials are medically accurate, evidence-based, and compliant with regulatory standards
  • Collaborate with Medical Affairs and Legal teams to ensure scientific content meets internal and external guidelines
    Additional responsibilities may include but are not limited to:
  • Leading MSL strategic initiatives/projects aligned with Medical Affairs and MSL organization strategy
  • Develop and implement scientific training plans for the MSL team
  • Mentorship of MSL peers
    Qualifications
  • Advanced degree (PhD, PharmD, MD) in life sciences or a related field (from An Accredited College or University).
  • Minimum of 2 years of experience in a Medical Affairs or MSL role within the pharmaceutical or biotech industry
  • Excellent understanding of sleep medicine and associated therapeutic areas strongly preferred
  • Exceptional verbal and written communication skills; ability to tailor scientific messages to diverse audiences and ability to interpret and communicate complex scientific data
  • Proven ability to build and maintain strong relationships with KOLs, investigators, and internal stakeholders
  • Strong understanding of clinical trial design, regulatory requirements, and therapeutic area landscape
  • Skilled in developing and delivering scientific presentations in various settings
  • Strong understanding of industry regulations and guidelines governing medical interactions
  • Ability to align field activities with broader medical and corporate strategies
  • Must have a valid driver's license with a driving record that meets company requirements
  • Willing and able to travel frequently throughout the Southeast region including Alabama, Arkansas, Florida, Georgia, Louisiana, Mississippi, South Carolina, Tennessee with primary coverage of major metropolitan and academic medical center markets across the region.
  • Must reside in the Atlanta metropolitan area or a major Florida metropolitan area with access to a major commercial airport to support frequent travel throughout the Southeast territory.ย 

Work Location

The Medical Science Liaison,ย Southeastย is a remote role based in the US, with up to 60-70% travel and occasional weekendsย 

Compensationย 

The annual base salary range for this position is $175,000.00 to $215,000.00. Individual compensation within this range will be determined based on a variety of factors, including qualifications, skills, relevant experience, job knowledge and location.ย 

In addition to base pay, this role is eligible for a discretionary annualย bonus.ย Centessa also offers a comprehensive benefits package, which includes a 401(k) plan, company-sponsored medical, dental, vision, and life insurance, generous paid time off, and a health and wellness program.ย 

POSITION: Full-Time, Exempt