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Associate Clinical Scientist Jobs in Decatur, GA

Natera

Associate Clinical Oncology Specialist

Atlanta, GA · On-site

$110K - $130K/yr

Northeast Atlanta The Associate Clinical Oncology Specialist (ACOS) is responsible for contributing ... scientists, business professionals, software engineers and many other professionals from world ...

Natera

Associate Clinical Oncology Specialist

Atlanta, GA · On-site

$110K - $130K/yr

Territory: Atlanta North The Associate Clinical Oncology Specialist (ACOS) is responsible for ... scientists, business professionals, software engineers and many other professionals from world ...

Natera

Associate Clinical Oncology Specialist

Atlanta, GA · On-site

$110K - $130K/yr

Northeast Atlanta The Associate Clinical Oncology Specialist (ACOS) is responsible for contributing ... scientists, business professionals, software engineers and many other professionals from world ...

Emory University

Clinical Track Faculty

Atlanta, GA

Woodruff Health Sciences Center of Emory University, the School of Nursing is a nationally ranked ... Candidates for consideration as Associate Professor or Professor should have an established track ...

Emory University

Clinical Track Faculty

Atlanta, GA · On-site

Woodruff Health Sciences Center of Emory University, the School of Nursing is a nationally ranked ... Candidates for consideration as Associate Professor or Professor should have an established track ...

Emory University

Clinical Track Faculty

Atlanta, GA · On-site

Woodruff Health Sciences Center of Emory University, the School of Nursing is a nationally ranked ... Candidates for consideration as Associate Professor or Professor should have an established track ...

Emory University

Clinical Track Faculty

Atlanta, GA · On-site

Woodruff Health Sciences Center of Emory University, the School of Nursing is a nationally ranked ... Candidates for consideration as Associate Professor or Professor should have an established track ...

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All JobsAssociate Clinical Scientist JobsAssociate Clinical Scientist Jobs in Decatur, GA

Associate Clinical Scientist information

See Decatur, GA salary details

$27

$53

$79

How much do associate clinical scientist jobs pay per hour?

As of Aug 20, 2026, the average hourly pay for associate clinical scientist in Decatur, GA is $53.45, according to ZipRecruiter salary data. Most workers in this role earn between $39.18 and $66.63 per hour, depending on experience, location, and employer.

What is an associate clinical scientist?

Associate Clinical Scientists are professionals who support the design, implementation, and monitoring of clinical trials and research studies in healthcare and pharmaceutical settings. They work closely with clinical teams to ensure that studies comply with regulatory requirements and scientific standards. Their responsibilities may include collecting and analyzing data, preparing reports, and assisting with protocol development. Typically, they have a background in life sciences and are involved in advancing medical research and improving patient care.

How does an associate clinical scientist typically collaborate with cross-functional teams during a clinical trial?

As an Associate Clinical Scientist, you will regularly work with multidisciplinary teams including clinical operations, data management, regulatory affairs, and biostatistics. Your role often involves supporting the design and execution of clinical studies, ensuring protocols are followed, and communicating scientific findings. Effective collaboration is key, as you may participate in team meetings, contribute to study documentation, and help resolve study-related issues. This collaborative environment fosters learning from experienced colleagues and provides a well-rounded view of the clinical development process.

What are the key skills and qualifications needed to thrive as an associate clinical scientist, and why are they important?

To thrive as an Associate Clinical Scientist, you need a solid foundation in biological sciences, analytical skills, and usually at least a bachelor's degree in a relevant field. Familiarity with laboratory information management systems (LIMS), statistical analysis tools, and regulatory standards such as GLP or GCP is typically expected. Strong attention to detail, teamwork, and effective written and verbal communication set exceptional candidates apart. These competencies ensure accurate data collection, regulatory compliance, and effective collaboration in clinical research environments.

What is the difference between Associate Clinical Scientist vs Clinical Research Associate?

AspectAssociate Clinical ScientistClinical Research Associate
Required CredentialsBachelor's or Master's in life sciences, relevant certificationsBachelor's in life sciences, often with certifications in clinical trials
Work EnvironmentResearch labs, pharmaceutical companies, biotech firmsClinical trial sites, hospitals, research organizations
Employer & Industry UsagePharmaceutical, biotech, medical device companiesContract research organizations, pharmaceutical companies
Common Search & ComparisonYesYes

The Associate Clinical Scientist and Clinical Research Associate roles share similarities in industry and required credentials, but differ mainly in work environment and focus. The Associate Clinical Scientist typically works in research labs or biotech firms focusing on data analysis and scientific development, while the Clinical Research Associate is more involved in monitoring clinical trials at trial sites. Both roles are essential in the clinical research process, with overlapping skills and industry usage.

What are popular job titles related to Associate Clinical Scientist jobs in Decatur, GA?

For Associate Clinical Scientist jobs in Decatur, GA, the most frequently searched job titles are:

What job categories do people searching Associate Clinical Scientist jobs in Decatur, GA look for?

The top searched job categories for Associate Clinical Scientist jobs in Decatur, GA are:

What cities near Decatur, GA are hiring for Associate Clinical Scientist jobs?

Cities near Decatur, GA with the most Associate Clinical Scientist job openings:

Associate Clinical Scientist jobs near you

Associate Clinical Site Lead - Atlanta

Abbott

Atlanta, GA • On-site

Full-time

Medical, Retirement

Re-posted 13 days ago

Abbott rating

7.8

Company rating: 7.8 out of 10

Based on 138 frontline employees who took The Breakroom Quiz

175th of 542 rated manufacturers

Job description

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 115,000 colleagues serve people in more than 160 countries.
JOB DESCRIPTION:
About Abbott
Abbott is a global healthcare leader, creating breakthrough science to improve people's health. We're always looking towards the future, anticipating changes in medical science and technology.
Working at Abbott
At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You'll also have access to:
  • Career development with an international company where you can grow the career you dream of.

  • Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year.

  • An excellent retirement savings plan with a high employer contribution

  • Tuition reimbursement, the Freedom 2 Save student debt program, and FreeU education benefit - an affordable and convenient path to getting a bachelor's degree.

  • A company recognized as a great place to work in dozens of countries worldwide and named one of the most admired companies in the world by Fortune.

  • A company that is recognized as one of the best big companies to work for as well as the best place to work for diversity, working mothers, female executives, and scientists.

The Opportunity
The Associate Clinical Site Lead for the Atlanta, GA region drives study execution and operational excellence across Abbott Cardiovascular therapies (Vascular, Cardiac Rhythm Management, EP, Structural Heart, and Heart Failure). Developing skills and foundation to become a resource in protocol execution, developing product and disease state knowledge, procedure support (as needed), procedure outcomes and early indication of trends, clinical trial enrollment, and ICH-GCP and clinical research application.
Adheres to specified site nomination, qualification, and startup processes. Leads ongoing training/retraining of all site stakeholders to ensure protocol adherence. Continuously reviews, manages, and influences all aspects of site's recruitment and data collection performance (enrollment, discrepancy resolution, compliance, etc.). Proactively utilizes appropriate operational metrics to minimize screen failure, attrition rate, etc. Monitors to ensure compliance with applicable regulatory requirements, Good Clinical Practice, and accuracy standards inclusive of site initiation, periodic, and close-out visits.
May be consulted in the following areas: study design, site payments, site audits, local document review, study documents preparation, and submission to site or competent authority/ethics committee.
What You'll Work On
With supervision of senior colleague/manager (or delegate):
Develop and maintain a productive clinical territory:
  • Identify, develop, and maintain sites capable of delivering start-up goals, study participation levels and required data quality.

  • Understand and assess investigators' interests and qualifications.

  • Identify appropriate investigators as defined by study-specific requirements and by the applicable regulatory code.

  • Maintain open communication and relationships with key site personnel including the Principle Investigator, Research Coordinator, as well as regulatory and legal personnel.

  • Provide ongoing technical support to customers and field staff.

  • Facilitate communication between clinical sites and other Abbott clinical staff (e.g., operations management, study team, Site Contracts Associate), as needed.

Manage all aspects of study lifecycle to include site regulatory and quality:
Start Up
  • Nominate, approach, and complete qualification processes including establishing site/sponsor expectations for study execution.

  • Facilitate all aspects of the start-up process and site initiation visits

  • Understand regulatory and legal requirements for study participation at a level that allows for appropriate collaboration with Abbott clinical staff, e.g. Site CRA, Site Contract Associate.

  • Train facility staff regarding protocol requirements and technology.

Enrollment
  • Develop site-specific strategies to promote appropriate patient enrollment.

  • Identify site successes and challenges and assist in implementing techniques that promote study goal achievement.

  • Continuously evaluate site study performance and provide timely feedback to site.

  • Attend study procedures and follow-ups when indicated (or ensure trained personnel attend).

Regulatory and Quality
  • Strong understanding of GCP and commitment to progress knowledge and achieve Abbott certifications

  • Develop site-specific strategies to avoid deviations.

  • Educate site on tools to facilitate compliance.

  • Provide timely feedback to the sites on key compliance indicators.

  • Escalate non-compliant sites according to corporate policy.

  • Collect essential documents, identify and obtain missing data, data corrections, reviewing adverse events and protocol deviations.

  • Review data and source documentation from investigational sites for accuracy and completeness

  • Facilitate resolution of data queries and action items at clinical sites

  • Promptly reports the findings of monitoring visits according to Abbott processes.

  • Maintain accurate, detailed and complete records of monitoring visits.

Provide training and procedure coverage:
  • Apply clinical and technical expertise to train site and Abbott staff for clinical trials and applicable commercial launches.

  • As needed, provide clinical and technical expertise for clinical trial procedure support

  • Attend study procedures and follow-ups (or ensure trained personnel attend).

Collaborate with commercial partners:
  • When appropriate, collaborate in the education of local sales groups on new product launches.

  • When appropriate, contribute to the education of customers on new and existing Abbott products.

  • Meet with key customers where Abbott GCO presence can elevate the customer experience.

  • Act as an additional resource for technical questions and troubleshooting.

Identify and adapt to shifting priorities and competing demands. Remain current on developments in the field of expertise including clinical and Abbott product knowledge, competitive positioning and published scientific and economic evidence.
  • Maintain at least one area of expertise and function as a local clinical and technical resource.

  • Develop working knowledge of disease states and product lines for all relevant Abbott clinical trials.

  • Upon leadership approval, complete and maintain certifications that are relevant to specific field(s) of expertise (where appropriate).

Education and Experience You'll Bring:
Required
  • Associate's degree

  • Minimum 1 year experience

Preferred
  • Bachelor's Degree in engineering, science, health science, nursing, or a related field, OR equivalent or related experience in cardiology or clinical research.

  • 2 years of progressively more responsible relevant clinical trial experience in the cardiovascular field.

  • Competency in catheterization lab and operating room protocol and procedures.

  • Possess independent problem-solving skills and ability to make decisions.

  • Exhibit excellent oral and written communication skills.

The base pay for this position is
$50,700.00 - $101,300.00
In specific locations, the pay range may vary from the range posted.
JOB FAMILY:
Clinical Affairs / Statistics
DIVISION:
MD Medical Devices
LOCATION:
United States of America : Remote
ADDITIONAL LOCATIONS:
WORK SHIFT:
Standard
TRAVEL:
Yes, 75 % of the Time
MEDICAL SURVEILLANCE:
No
SIGNIFICANT WORK ACTIVITIES:
Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day), Driving a personal auto or company car or truck, or a powered piece of material handling equipment, Keyboard use (greater or equal to 50% of the workday)
Abbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans.
EEO is the Law link - English: http://webstorage.abbott.com/common/External/EEO_English.pdf
EEO is the Law link - Espanol: http://webstorage.abbott.com/common/External/EEO_Spanish.pdf

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