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Clinical Study Associate Jobs in Decatur, GA (NOW HIRING)

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Clinical Study Associate information

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$53

How much do clinical study associate jobs pay per hour?

As of Jul 14, 2026, the average hourly pay for clinical study associate in Decatur, GA is $30.79, according to ZipRecruiter salary data. Most workers in this role earn between $20.67 and $40.62 per hour, depending on experience, location, and employer.

What are Clinical Study Associates?

Clinical Study Associates (CSAs) are professionals who support the planning, execution, and monitoring of clinical trials in the pharmaceutical, biotechnology, or medical device industries. They help coordinate study logistics, maintain study documentation, and ensure compliance with regulatory requirements. CSAs often work closely with Clinical Research Associates, study coordinators, and investigators to ensure that trials are conducted according to protocol and timelines. Their role is essential in ensuring the accuracy and integrity of data collected during clinical research.

What is the difference between Clinical Study Associate vs Clinical Research Coordinator?

AspectClinical Study AssociateClinical Research Coordinator
CredentialsBachelor's degree, often in life sciences; certifications like CCRP or CCRA beneficialBachelor's degree in health sciences or related field; certifications like CCRP advantageous
Work EnvironmentPharmaceutical companies, CROs, clinical trial sitesHospitals, clinics, research centers
Job FocusMonitoring clinical trials, ensuring protocol compliance, data accuracyManaging daily trial activities, patient recruitment, data collection
Employer & Industry UsageCommonly employed in pharma and CROsPrimarily in healthcare and academic research settings

Both roles involve clinical trial oversight but differ in focus: Clinical Study Associates primarily monitor and ensure compliance during trials, while Clinical Research Coordinators manage daily trial operations and patient interactions. Understanding these distinctions helps in choosing the right career path or job search focus.

What are the key skills and qualifications needed to thrive as a Clinical Study Associate, and why are they important?

To thrive as a Clinical Study Associate, you need a strong understanding of clinical research processes, regulatory requirements, and typically a life sciences degree. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and GCP certification are commonly required. Attention to detail, organizational skills, and effective communication set top performers apart in this role. These competencies ensure accurate study documentation, regulatory compliance, and smooth coordination across research teams.

What are some common challenges Clinical Study Associates face when managing multiple clinical trials simultaneously?

Clinical Study Associates often juggle several clinical trials at once, which can present challenges such as prioritizing competing deadlines, maintaining accurate documentation for each study, and ensuring consistent communication with cross-functional teams. Staying organized and proactive is essential, as unforeseen protocol amendments or site issues can arise. Building strong relationships with site staff and utilizing effective project management tools can help CSAs navigate these complexities and deliver high-quality results.
What are the most commonly searched types of Clinical Study jobs in Decatur, GA? The most popular types of Clinical Study jobs in Decatur, GA are:
What cities near Decatur, GA are hiring for Clinical Study Associate jobs? Cities near Decatur, GA with the most Clinical Study Associate job openings:
Clinical Study Associate jobs near you
Infographic showing various Clinical Study Associate job openings in Decatur, GA as of July 2026, with employment types broken down into 1% As Needed, 66% Full Time, 29% Part Time, 2% Temporary, and 2% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $64,051 per year, or $30.8 per hour.
Patient Liaison Supervisor

Patient Liaison Supervisor

Alcanza Clinical Research

Decatur, GA • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 13 days ago

Job description

Description
Alcanza is a growing multi-site, multi-phase clinical research company with a network of locations in AL, AZ, FL, GA, IL, MA, MI, MO, NV, SC, TX, VA, and Puerto Rico. We have established a strong presence across Phase I-IV studies and several therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general medicine. Join us as we continue to grow.
The Manager, Patient Liaison Services is responsible for leading and supporting a team of onsite patient recruitment professionals to identify, engage, and enroll eligible participants in clinical trials. This role plays a critical part in optimizing recruitment strategies across multiple therapeutic areas and works collaboratively with site and regional directors, study teams, investigators, marketing, and community outreach partners to ensure recruitment goals are met efficiently and ethically.

Key Responsibilities
Essential Job Duties:
  • Manage the patient liaison function with a focus on driving recruitment, monitoring performance metrics, and meeting site & regional recruitment targets and needs.
  • Manage, direct, and train on the activities of the assigned patient liaison team; routinely assess study-specific processes and site needs, evaluate training needs and compliance, drive screening numbers and output, and ensure the quality of scheduled appointments.
  • Monitor, collect, and report on performance metrics including outbound calling, patient scheduling, completed appointments, DNQ rates, quality of calls and appointments made, and overall key performance metrics for team(s).
  • Collaborate with regional management, site leadership, and other team members/departments to optimize Patient Liaisons' performance to meet site and regional goals.  Communicate and liaise with teams, patients, and clients (internal & external) in a timely and professional manner.
  • Develop and oversee strategic recruitment plans targeting priority studies of specific populations to meet study enrollment goals. 
  • Ensure team members are well-versed in all active clinical trials and understand relevant therapeutic indications. 
  •  Utilize CTMS to monitor and triage no-shows and screen failures (DNQs) and generate targeted call lists. 
  • Promote and manage referral initiatives such as “Refer-A-Friend” campaigns. 
  • Equip staff with multi-study recruitment tools to support cross-therapeutic enrollment success. 
  • Support eligibility assessments through prescreening interviews and collaboration with clinical staff. 
  • Monitor site and regional recruitment metrics, adjusting strategies as needed to meet performance targets. 
  • Contribute to site, regional, and organizational initiatives aimed at improving recruitment operations. 
  • Maintain and optimize tracking systems for no-shows and DNQs. 
  • Provide prescreening logs and recruitment updates to sponsors, offering strategic input to support enrollment objectives. 
  • Coordinate with site staff, cross-functional teams, and investigators to ensure seamless recruitment workflows.
  • Build and manage relationships with community organizations, HCP providers, and advocacy groups.  
  • Develop culturally sensitive recruitment approaches to reach diverse populations. 
  • Organize, present, and attend ongoing outreach events (on-site and off-site)  to raise awareness of clinical trials.  
  • Coordinate and train the Patient Liaison team to effectively build and manage community relationships and actively participate in outreach events. 
  • Draft and distribute ongoing newsletters to engage current and potential study participants, leveraging CTMS for targeted communications.
  • Collaborate with Alcanza marketing team to execute digital and print campaigns and manage marketing materials for outreach events.  
  • Responsible for all people management activities including staff scheduling to ensure optimal coverage, interviewing and selection, performance appraisals & goal setting, timecard, PTO and payroll needs, employee counseling, new hire onboarding and training, and career development. Manage and mentor assigned staff, proactively identify and resolve issues, and work to ensure successful team operations.  
  • Manage and communicate enrollment goals and timelines as aligned with business needs.
  • Handle escalated patient calls, inquiries, or issues.  Escalate issues as appropriate. 
  • Employ strategic thinking and problem-solving skills to propose and implement risk mitigations.
  • Maintain a high level of knowledge regarding study mix and resource availability at each site.
  • Ensure function activities comply with regulatory guidelines, study requirements, & company policies.
  • Lead, participate, and/or present in team, site, operations, management, client, or other meetings.
  • Perform other related duties as assigned.


Skills, Knowledge and Expertise
Minimum Qualifications:  An associate’s degree AND a minimum of 3 years’ related experience, or an equivalent combination of education and experience, is required.  3+ years’ experience in healthcare or clinical research recruitment and patient engagement is required.  Must have a strong understanding of clinical trial processes and applicable regulatory requirements.  Prior experience with therapy areas, customer service, scheduling and CTMS (Clinical Trial Management Systems) is highly preferred.  1+ years’ experience with people management is highly preferred.  Familiarity with digital marketing, CRM systems, and recruitment analytics is a plus. 
Required Skills: 
  • Proficiency with computer applications such as Microsoft applications, email, web applications, and the ability to type proficiently (40+ wpm)
  • Must possess strong organizational, time management, problem-solving, presentation, and project management skills.
  • Well-developed written and verbal communication and presentation skills, with the ability to effectively convey complex concepts to diverse audiences.  
  • Well-developed interpersonal and listening skills and the ability to work well independently, collaboratively, and professionally within a team environment, with clients and all stakeholders (internal & external), and with all levels within the organization.
  • Must be detail-oriented, possess a high degree of professionalism, integrity, dependability, respect of others, self-motivation, and exemplify a strong work ethic.
  • Must have the ability to thrive in a fast-paced, deadline-driven environment
  • Ability to work under minimal supervision, identify problems and implement solutions.
  • Ability to handle highly sensitive information in a confidential and professional manner, and in compliance with HIPAA guidelines.

Benefits
  • Full-time employees regularly scheduled to work at least 30 hours per week are benefits-eligible, with coverage starting on the first day of the month following date of hire. 
  • Medical, dental, vision, life insurance, short and long-term disability insurance, health savings accounts, supplemental insurances, and a 401k plan with a safe harbor match are offered.