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Full Time Human Subject Research Jobs in Decatur, GA

CenExel

Clinical Research Coordinator

Decatur, GA · On-site

$23.75 - $31.50/hr

... full time employees after 30 days of employment including Health Insurance, Dental, Vision, LTD ... Knowledge and understanding of Federal regulations protecting human subjects in research and that ...

Chick-fil-A

Senior Human Resources Coordinator

Atlanta, GA

$19.75 - $25.75/hr

Position Type: * Full-time Our Benefits Include: * Competitive Pay - Along with a competitive ... Research and file Worker's Compensation claims * Research and file guest claims * Track attendance ...

Chick-fil-A

Senior Human Resources Coordinator

Atlanta, GA · On-site

$19.75 - $25.75/hr

Position Type: * Full-time Our Benefits Include: * Competitive Pay - Along with a competitive ... Research and file Worker's Compensation claims * Research and file guest claims * Track attendance ...

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All JobsHuman Subject Research JobsFull Time Human Subject Research JobsFull Time Human Subject Research Jobs in Decatur, GA

Full Time Human Subject Research information

What are the key skills and qualifications needed to thrive in Full Time Human Subject Research, and why are they important?

To thrive in Full Time Human Subject Research, you need a solid background in scientific methodology, ethical research practices, and often a degree in a relevant field such as psychology, biology, or public health. Familiarity with data collection tools, statistical software (like SPSS or R), and Institutional Review Board (IRB) protocols is typically required. Exceptional attention to detail, strong interpersonal skills, and clear communication help ensure accurate data collection and ethical participant interactions. These skills and qualities are crucial for producing valid research outcomes while safeguarding participant rights and well-being.

What is a Full Time Human Subject Researcher?

A Full Time Human Subject Researcher is a professional who conducts scientific studies involving human participants. Their work typically includes designing research protocols, recruiting and monitoring subjects, collecting data, and ensuring all research is conducted ethically and in compliance with regulations. They may work in academic, clinical, or private research settings and often collaborate with other scientists and medical professionals. The goal is to advance knowledge in fields such as medicine, psychology, or public health, while prioritizing the safety and rights of human subjects.

What are the typical challenges faced by professionals in full-time human subject research roles?

Professionals working in full-time human subject research often face challenges such as recruiting and retaining participants, ensuring strict compliance with ethical guidelines and institutional review board (IRB) protocols, and managing sensitive data securely. Balancing administrative tasks with hands-on research activities can also be demanding, as can coordinating with multidisciplinary teams including clinicians, statisticians, and regulatory staff. Strong organizational skills and adaptability are key to successfully navigating these complexities while maintaining the integrity of the study.

What is the difference between Full Time Human Subject Research vs Full Time Clinical Research Coordinator?

AspectFull Time Human Subject ResearchFull Time Clinical Research Coordinator
CredentialsOften requires a bachelor's degree in health sciences, psychology, or related fields; certifications like CITI are commonTypically requires a bachelor's degree; certifications like CITI or CCRP are advantageous
Work EnvironmentResearch institutions, universities, hospitals conducting human subject studiesClinical trial sites, hospitals, research centers managing patient studies
Employer & IndustryAcademic, government, or private research organizationsPharmaceutical companies, hospitals, clinical research organizations

Both roles involve working with human subjects in research settings, but Full Time Human Subject Research often focuses on designing and analyzing studies, while Clinical Research Coordinators manage day-to-day trial operations. Understanding these differences helps job seekers identify the right career path in clinical research.

What are the most commonly searched types of Human Subject Research jobs in Decatur, GA? The most popular types of Human Subject Research jobs in Decatur, GA are:
What are popular job titles related to Full Time Human Subject Research jobs in Decatur, GA? For Full Time Human Subject Research jobs in Decatur, GA, the most frequently searched job titles are:
What job categories do people searching Full Time Human Subject Research jobs in Decatur, GA look for? The top searched job categories for Full Time Human Subject Research jobs in Decatur, GA are:
What cities near Decatur, GA are hiring for Full Time Human Subject Research jobs? Cities near Decatur, GA with the most Full Time Human Subject Research job openings:
Full Time Human Subject Research jobs near you
Clinical Research Coordinator

Clinical Research Coordinator

CenExel

Decatur, GA • On-site

$23.75 - $31.50/hr

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted yesterday

Job description

About Us:
CenExel is a leading nationwide clinical research site and patient network serving the life sciences industry. Leading in CNS and early phase studies, our 18 science-led Centers of Excellence deliver the right patients, at the right time, in the right place. Recently acquired by BayPine Capital Partners, our research sites provide unparalleled medical and scientific support in the design and execution of clinical trials. Our world-class PIs, advanced patient engagement strategies, premium data analytics, and integrated operations optimize every step of the clinical trial process.
Along with an exceptional work environment that promotes teamwork, positive leadership, and optimal work-life balance, CenExel Clinical Research also provides highly competitive compensation and a generous benefits package to full time employees after 30 days of employment including Health Insurance, Dental, Vision, LTD, STD, Life Ins, and 401k.
Job Summary:
Responsible for coordinating all aspects of clinical trials with the strictest adherence to ICH (International Conference on Harmonization), GCP (Good Clinical Practices), protocol, and company guidelines, regulations, and policies.
Essential Responsibilities and Duties:
  • Under supervision, coordinates aspects of patient involvement for complex and/or multiple studies from study initiation until study completion.
  • Organizes research information for clinical trials.
  • Observes subjects and assists with data analysis and reporting.
  • Schedules the collection of data.
  • Reviews, and reports adverse events, protocol deviations, and other unanticipated problems appropriately.
  • Monitors, and reports research data to maintain quality and compliance.
  • Performs administrative and regulatory duties related to the study as appropriate.
  • Participates in other protocol development activities.
  • Ensures site receives accurate information and supplies from sponsors (i.e.: source, protocol, scales, supplies, approvals, contacts, etc.)
  • Educates potential participants and caregivers on protocol specific details and expectations.
  • Performs safety and efficacy assessments per protocol (vital signs, EKGs, blood draws and other assessments as assigned).
  • Assists Clinical Trial Manager (CTM) with oversight of vendors, accounting, regulatory, client satisfaction, recruitment, quality, and trial outcomes.
  • Assists the CTM in planning, creating processes, trainings and development of staff.
  • Assumes other duties and responsibilities as assigned. The above responsibilities are a general description of the level and nature of the work assigned to this classification and are not to be considered as all inclusive.

Education/Experience/Skills:
  • Must have proper experience and demonstrate mastery of Clinical Research Coordinator I position.
  • High school graduate or equivalent; Bachelors Degree, preferred
  • CCRC certification preferred
  • 2-3 years of experience in the medical field, preferred
  • Knowledge and understanding of Federal regulations protecting human subjects in research and that govern the conduct of clinical trials.
  • Strong leadership and mentorship skills.
  • Developing and maintaining effective working relationships at all levels of the organization, along with those at the sponsor and vendor level.
  • Crisis management and problem solving skills; ability to react calmly and effectively in emergent situations.
  • Works independently as well as functioning as part of a team.
  • Must be able to effectively communicate verbally and in writing.

Working Conditions
  1. Indoor, Office environment.
  2. Shift work, depending on location.
  3. Essential physical requirements include sitting, typing, standing, and walking.
  4. Lightly active position, occasional lifting of up to 20 pounds.
  5. Reporting to work, as scheduled, is essential.
  6. Overnight travel may be required for training and/or investigative meetings.

CenExel Clinical Research is an Equal Opportunity Employer. All applicants will be considered for employment without regards to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or status.
Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.

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