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Psychiatric Research Assistant Jobs in Decatur, GA

Hightop Health

Clinical Research Coordinator

Marietta, GA · On-site

$23 - $30.50/hr

Our Integrative Psychiatry services are designed to treat the whole person, optimizing our patients ... capture. * Assist practice staff with clinical tasks as directed, including blood pressure ...

Alcanza

Clinical Research Coordinator

Decatur, GA · On-site

$23.75 - $31.50/hr

... dermatology, psychiatry, and general medicine. Join us as we continue to grow. The Clinical ... May assist with study recruitment, patient enrollment, and tracking as needed; * Maintaining ...

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How much do psychiatric research assistant jobs pay per hour?

As of May 30, 2026, the average hourly pay for psychiatric research assistant in Decatur, GA is $21.73, according to ZipRecruiter salary data. Most workers in this role earn between $16.88 and $25.34 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Psychiatric Research Assistant, and why are they important?

To thrive as a Psychiatric Research Assistant, you need a background in psychology or a related field, with experience in research methods, data collection, and analysis. Familiarity with statistical software (such as SPSS or R), IRB protocols, and data management systems is typically required. Strong organizational skills, attention to detail, and the ability to communicate effectively with research participants and team members are crucial soft skills. These competencies ensure accurate, ethical, and efficient research processes that contribute to meaningful findings in psychiatric studies.

What are some common challenges faced by psychiatric research assistants during clinical studies?

Psychiatric research assistants often encounter challenges such as recruiting and retaining participants who may have complex mental health needs. Additionally, managing sensitive data and maintaining strict confidentiality can require extra diligence. Balancing administrative tasks, such as scheduling assessments and entering data, with direct participant interaction is also common. Effective communication with multidisciplinary teams, including clinicians and principal investigators, is essential for ensuring studies run smoothly.

What are Psychiatric Research Assistants?

Psychiatric Research Assistants are professionals who support research projects related to mental health and psychiatric disorders. They assist in tasks such as recruiting study participants, collecting and managing data, administering assessments, and maintaining research documentation. Their work helps advance scientific understanding of mental illnesses and the effectiveness of treatments. These assistants often work in hospitals, universities, or research institutes under the supervision of principal investigators. A background in psychology, neuroscience, or a related field is typically required.

What is the difference between Psychiatric Research Assistant vs Clinical Research Coordinator?

AspectPsychiatric Research AssistantClinical Research Coordinator
Required CredentialsTypically a bachelor's degree in psychology, neuroscience, or related field; some roles may require certificationUsually a bachelor's degree; certification in clinical research may be preferred
Work EnvironmentResearch labs, hospitals, mental health clinicsClinical trial sites, hospitals, research institutions
Employer & Industry UsageAcademic institutions, mental health research centersPharmaceutical companies, hospitals, research organizations
Common Search & Comparison IntentUnderstanding entry-level research roles in psychiatryManaging clinical trials and patient coordination

The Psychiatric Research Assistant primarily supports research studies in mental health settings, focusing on data collection and analysis. In contrast, the Clinical Research Coordinator manages the overall conduct of clinical trials, including patient recruitment and regulatory compliance. Both roles require similar educational backgrounds but differ in responsibilities and work environments.

What job categories do people searching Psychiatric Research Assistant jobs in Decatur, GA look for? The top searched job categories for Psychiatric Research Assistant jobs in Decatur, GA are:
What cities near Decatur, GA are hiring for Psychiatric Research Assistant jobs? Cities near Decatur, GA with the most Psychiatric Research Assistant job openings:
Psychiatric Research Assistant jobs near you
Infographic showing various Psychiatric Research Assistant job openings in Decatur, GA as of May 2026, with employment types broken down into 21% Full Time, and 79% Part Time. Highlights an 96% Physical, 3% Hybrid, and 1% Remote job distribution, with an average salary of $45,208 per year, or $21.7 per hour.
Clinical Research Coordinator

Clinical Research Coordinator

Alcanza Clinical Research

Decatur, GA • On-site

$23.75 - $31.50/hr

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 23 days ago

Job description

Clinical Research Coordinator
Department: Operations
Employment Type: Full Time
Location: Accel Research Sites - Decatur, GA
Reporting To: Benoit Tete
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 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 collaboration with other members of the clinical research site team, works to ensure the execution of assigned studies. Responsibilities may include but are not limited to:
  • Screening of patients for study enrollment;
  • Patient consents;
  • Patient follow-up visits;
  • Documenting in source clinic charts;
  • Entering data in EDC and answers queries;
  • Obtaining vital signs and ECGs;
  • May perform basic lab procedures per protocol, such as: blood specimen collection, centrifuge operation, storing and shipping of lab specimens, accountability of specimens and notification of courier for specimen pick-up;
  • Requesting and tracking medical record requests;
  • Updating and maintaining logs, chart filings;
  • Maintaining & ordering study specific supplies;]
  • Scheduling subjects for study visits and conducts appointment reminders;
  • Building/updating source as needed;
  • Conducting monitoring visits and resolves issues as needed in a timely manner;
  • Ensuring study related reports and patient results are reviewed by investigator in a timely manner;
  • Filing SAE/Deviation reports to Sponsor and IRB as needed;
  • Documenting and reporting adverse events;
  • Reporting non-compliance to appropriate staff in timely manner;
  • Maintaining positive and effective communication with clients and team members;
  • Always practicing ALCOAC principles with all documentation;
  • May assist with study recruitment, patient enrollment, and tracking as needed;
  • Maintaining confidentiality of patients, customers and company information, and;
  • Performing all other duties as requested or assigned.
  • Complete all needed activities for study start-up, including completing required training, uploading / printing certificates to file in ISF, etc.;
  • Prepare and attend site initiation visits (SIV's) and Investigator Meetings (IMs), as needed;
  • May set up, train and maintain all technology needed for studies.

Skills, Knowledge and Expertise
Minimum Qualifications: A Medical Assistant diploma, LPN/LVN, EMT credential OR Associate's degree AND a minimum of 1 year of clinical research or clinical experience, OR an equivalent combination of education and experience, is required. Proficiency with performing basic clinical procedures such as (blood pressure, vitals, EKGs, phlebotomy, etc.) is highly preferred. Bi-lingual (English / Spanish) proficiency is a plus.
Required Skills:
  • Proficiency with computer applications such as Microsoft applications, email, electronic health records, web applications, and the ability to type proficiently (40+ wpm);
  • Performing basic clinical procedures such as blood pressure, vitals, EKGs, phlebotomy, etc
  • Strong organizational skills and attention to detail.
  • Well-developed written and verbal communication skills.
  • Well-developed interpersonal and listening skills and the ability to work well independently as well as with co-workers, subjects, managers and external customers.
  • Ability to effectively handle multiple tasks, and adapt to changes in workloads and priorities.
  • Must be professional, respectful of others, self-motivated, and have a strong work ethic.
  • Must possess a high degree of integrity and dependability.
  • 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.

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