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Assistant International Clinical Research Jobs in Decatur, GA

Alcanza

Clinical Research Assistant

Decatur, GA · On-site

The Research Assistant (RA) provides support to the Clinical Research Coordinators (CRCs), Site Manager, Principal and Sub Investigators, and other site staff in compliance with GCP, ICH, HIPAA, FDA ...

Denali Health

Clinical Research Nurse

Atlanta, GA · On-site

Coordinate with Principal Investigators, study coordinators, sponsors, and CROs * Assist with ... Previous clinical research experience * CCRP (Certified Clinical Research Professional) or ACRP ...

Denali Health

Clinical Research Nurse

Atlanta, GA · On-site

Coordinate with Principal Investigators, study coordinators, sponsors, and CROs * Assist with ... Previous clinical research experience * CCRP (Certified Clinical Research Professional) or ACRP ...

Georgia Retina

Clinical Research Coordinator

Marietta, GA · On-site

$23 - $30.50/hr

Position Summary We are now hiring for a Clinical Research Assistant that will support a high-volume Research Department within an ophthalmic practice that focuses on providing quality and ...

Actalent

Clinical Research Coordinator

Atlanta, GA · On-site

$22 - $25/hr

... and materials. * Assist with documentation, including completion of study forms, logs, and ... Clinical research experience, including at least one year in a clinical research setting; academic ...

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Actalent

Clinical Research Coordinator

Atlanta, GA · On-site

$22 - $25/hr

... and materials. * Assist with documentation, including completion of study forms, logs, and ... Clinical research experience, including at least one year in a clinical research setting; academic ...

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Assistant International Clinical Research information

See Decatur, GA salary details

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How much do assistant international clinical research jobs pay per hour?

As of Aug 20, 2026, the average hourly pay for assistant international clinical research in Decatur, GA is $19.75, according to ZipRecruiter salary data. Most workers in this role earn between $16.20 and $22.79 per hour, depending on experience, location, and employer.

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

AspectAssistant International Clinical ResearchClinical Research Coordinator
Required CredentialsTypically a bachelor's degree, some roles may require certification in clinical researchUsually a bachelor's degree, often with certification like CCRP or CCRC
Work EnvironmentGlobal or international settings, often in pharmaceutical or biotech companiesHospital, clinic, or research site settings
Employer & Industry UsagePharmaceutical companies, CROs, biotech firms conducting international trialsHospitals, academic institutions, research sites
Common Search & ComparisonYesYes

Assistant International Clinical Research roles focus on supporting global clinical trials, often requiring knowledge of international regulations. Clinical Research Coordinators manage local trial activities at research sites. While both roles require similar educational backgrounds and certifications, their work environments and scope differ, with the assistant role emphasizing international coordination and the coordinator role focusing on site-level trial management.

What are popular job titles related to Assistant International Clinical Research jobs in Decatur, GA?

For Assistant International Clinical Research jobs in Decatur, GA, the most frequently searched job titles are:

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

The top searched job categories for Assistant International Clinical Research jobs in Decatur, GA are:

Assistant International Clinical Research jobs near you

Clinical Research Coordinator

Alcanza Clinical Research

Decatur, GA • On-site

$23.75 - $31.50/hr

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 15 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, VA, SC, TN, TX 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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