ZipRecruiter

Log In

1

Clinical Research Trainee Jobs in Decatur, GA (NOW HIRING)

Emory University

Post Doctoral Fellow

Atlanta, GA · Hybrid

$48K - $65K/yr

Description This clinical-research-focused postdoctoral position is focused on optimizing ... The specific area of research in which the trainee is mentored is determined by the department and ...

Emory University

Post Doctoral Fellow

Atlanta, GA · On-site

$48K - $65K/yr

Description This clinical-research-focused postdoctoral position is focused on optimizing ... The specific area of research in which the trainee is mentored is determined by the department and ...

Emory University

Post Doctoral Fellow

Atlanta, GA · Hybrid

$48K - $65K/yr

This clinical-research-focused postdoctoral position is focused on optimizing psychedelic ... The specific area of research in which the trainee is mentored is determined by the department and ...

Emory University

Post Doctoral Fellow

Atlanta, GA · On-site

$47K - $64K/yr

The fellow will work with an interdisciplinary team of clinical psychologists, basic ... The specific area of research in which the trainee is mentored is determined by the department and ...

Emory University

Post Doctoral Fellow

Atlanta, GA · On-site

$47K - $64K/yr

The fellow will work with an interdisciplinary team of clinical psychologists, basic ... The specific area of research in which the trainee is mentored is determined by the department and ...

Emory University

Post Doctoral Fellow

Atlanta, GA · On-site

$47K - $64K/yr

The fellow will work with an interdisciplinary team of clinical psychologists, basic ... The specific area of research in which the trainee is mentored is determined by the department and ...

next page

Showing results 1-20

All JobsClinical Research JobsClinical Research Trainee JobsClinical Research Trainee Jobs in Decatur, GA

Clinical Research Trainee information

What is a clinical research trainee?

Clinical Research Trainees are individuals, often students or recent graduates, who are gaining practical experience in the field of clinical research. They assist in the design, implementation, and monitoring of clinical trials under the supervision of experienced researchers. Their responsibilities may include data collection, managing study documentation, ensuring compliance with regulatory guidelines, and supporting patient recruitment. The role provides foundational knowledge and hands-on skills necessary for a career in clinical research or related healthcare fields.

What are the key skills and qualifications needed to thrive as a clinical research trainee, and why are they important?

To thrive as a Clinical Research Trainee, you need a solid background in life sciences or healthcare, attention to detail, and a foundational understanding of research methodologies, typically supported by a relevant degree. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) guidelines, and clinical trial management software is essential. Strong organizational skills, effective communication, and the ability to collaborate within multidisciplinary teams are standout soft skills. These competencies ensure that clinical trials are conducted ethically, efficiently, and in compliance with regulatory standards.

What are the typical responsibilities of a clinical research trainee during a clinical trial?

As a Clinical Research Trainee, you will typically assist with the coordination and execution of clinical trials under the supervision of experienced research staff. Your daily tasks may include collecting and managing patient data, assisting with patient recruitment and informed consent, preparing study documentation, and ensuring compliance with regulatory guidelines. Trainees often collaborate closely with clinical teams, principal investigators, and external partners, gaining hands-on experience across various study phases. This role provides valuable exposure to clinical research protocols and is a great foundation for advancing into more senior research or coordinator positions.

What is the difference between Clinical Research Trainee vs Clinical Research Coordinator?

AspectClinical Research TraineeClinical Research Coordinator
Required CredentialsTypically pursuing or holding a relevant degree (e.g., life sciences, healthcare)Usually has a degree or certification in clinical research or related field
Work EnvironmentTraining setting, often in academic or research institutionsActive role in managing clinical trials at research sites or hospitals
Employer & Industry UsageEducational programs, research institutions, pharmaceutical companiesHospitals, clinics, research organizations
Common Search & Comparison IntentUnderstanding entry-level roles and training opportunitiesClarifying responsibilities and career progression in clinical research

While both roles are involved in clinical research, a Clinical Research Trainee is typically in a learning or internship phase, gaining foundational knowledge. In contrast, a Clinical Research Coordinator actively manages and oversees clinical trials, requiring more experience and responsibility.

What are the most commonly searched types of Clinical Research jobs in Decatur, GA? The most popular types of Clinical Research jobs in Decatur, GA are:
What job categories do people searching Clinical Research Trainee jobs in Decatur, GA look for? The top searched job categories for Clinical Research Trainee jobs in Decatur, GA are:
Clinical Research Trainee jobs near you
Infographic showing various Clinical Research Trainee job openings in Decatur, GA as of August 2026, with employment types broken down into 100% Full Time. Highlights an 60% In-person, and 40% Remote job distribution.

Agile Clinical Trial (ACT) Trng Prgm Oncology Non-Physician Practitioner Preceptor

Morehouse School of Medicine

Atlanta, GA • On-site

Full-time

Re-posted 18 days ago

Job description

Posting Details
Position Information
About MSM
Morehouse School of Medicine (MSM) is a place of distinction, serving as the nation's leading academic medical center for vulnerable populations. It's also a place for passionate individuals looking to join a dedicated community working today to help prepare tomorrow's leaders.
We exist to:
• Improve the health and well-being of individuals and communities;
• Increase the diversity of the health professional and scientific workforce;
• Address primary health care through programs in education, research and service;
With emphasis on people of color and the under-served urban and rural populations in Georgia, the nation and the world.
At Morehouse School of Medicine, we're leading the creation and advancement of health equity. You will find a fulfilling career at MSM!
Posting Number
NONAC3623
Job Title
Agile Clinical Trial (ACT) Trng Prgm Oncology Non-Physician Practitioner Preceptor
Position Title
Agile Clinical Trial (ACT) Training Program Manager
Position Type
Non-Faculty
Number of vacancies
1
Salary
Commensurate with experience
Department
Cancer Health Equity Institute
Position Summary
Morehouse School of Medicine (MSM) is seeking a motivated, detail-oriented Oncology Non-Physician Practitioner Preceptor to support the Agile Clinical Trial (ACT) Education & Training Program. This position is a crucial part of the ACT program, which aims to establish a comprehensive, sustainable pipeline of clinical research professionals. The Oncology Non-Physician Practitioner Preceptor will be responsible for supervising and training program participants during their clinical practicum, specifically within the oncology setting. You are not just an instructor; you are a coach, a role model, and a vital bridge between theoretical knowledge and the real-world practice of clinical research. Your expertise will ensure our graduates are fully prepared to excel in roles such as Clinical Research Coordinators (CRCs) and Clinical Trial Advanced Practice Provider.
POSITION ACCOUNTABILITIES AND ESSENTIAL FUNCTIONS:
  1. Clinical Mentorship & Training: Supervise trainees during their 16-week clinical practicum in oncology clinics and infusion centers. Provide direct, hands-on supervision and precepting to trainees in a clinical research setting (e.g., clinic, investigational site). Model best practices in patient safety, ethical conduct, and compassionate care within a research context. Serve as a professional role model for clinical research excellence, critical thinking, and professional communication.

  1. Practical Training Delivery: Provide hands-on training to trainees, allowing them to gain practical, in-person experience with oncology patients and infusion unit equipment.

• Patient screening, recruitment, and informed consent processes.
• Administration of investigational products/therapies.
• Phlebotomy and sample processing per protocol specifications.
• Accurate and timely documentation in source documents and case report forms (CRFs).
• Management of adverse events (AEs) and serious adverse events (SAEs).
• Protocol-specific patient assessments and data collection.
  1. Skill Development: Assisting trainees in developing essential skills such as patient recruitment and retention in a clinical environment. Collaborate with the program staff to develop and refine practical, simulation-based training modules.
  2. Evaluation and Feedback: Reinforce and provide realistic clinical scenarios to help trainees develop critical thinking and problem-solving skills. Closely observe trainee performance and provide constructive, timely, and objective feedback on trainee professionalism, initiative, and observation skills. Complete trainee performance evaluations and contribute to decisions regarding progression in the program. Quickly identify struggling trainees and develop individualized remediation plans.
  3. Operational Training: Co-facilitate classroom and skills lab sessions on clinical procedures, Good Clinical Practice (GCP), and protocol adherence. Orient trainees to the oncology clinic and infusion center workflows. This includes familiarizing trainees with the equipment and procedures used in oncology.

Knowledge, Skills, & Abilities
  • A strong understanding of clinical research processes and human subjects research and protections.
  • Familiarity with oncology trials and precision medicine concepts, particularly related to genomic testing and clinical trial matching.
  • Knowledge of clinical trial regulatory requirements (IRB, HIPAA, GCP, etc.).
  • Working knowledge of electronic health records (EHRs), clinical trial management systems (CTMS), and data entry protocols.
  • Awareness of ethical considerations related to the informed consent process and data privacy.
  • The ability to build and maintain positive working relationships across interdisciplinary teams.
  • The ability to adapt quickly to changes in program needs, study protocols, and technology platforms.

SUPERVISORY RESPONSIBILITIES:
This position may be responsible for supervising trainees and interns within a project.
Minimum Qualifications
  • Bachelor of Science in Nursing (BSN) from a regionally accredited college or university.
  • Current and unrestricted medical license.
  • Minimum of 2 years of direct hands-on experience as a Clinical Research Coordinator
    1. In-depth, practical knowledge of ICH-GCP guidelines, FDA regulations, and human subject protection.
    2. Proven experience with clinical procedures common in research (IV insertion, phlebotomy, ECG, vital signs, drug administration).
    3. Demonstrated experience in precepting, mentoring and training research staff.
    4. Strong organizational skills and attention to detail.
    5. Ability to prioritize tasks and work independently, as well as part of a team.
    6. Excellent communication and interpersonal skills.
    7. Experience with clinical trial processes and data management systems.
    8. Excellent analytical, problem-solving, and organizational skills.

Preferred Qualifications
  • Master of Science in Physician Assistant Studies (MSPA or MSPAS), MBBS (Bachelor of Medicine, Bachelor of Surgery), Doctor of Osteopathic Medicine (DO) or Doctor of Medicine (MD)

Closing Date
Open Until Filled
Yes
Special Instructions to Applicants
Employment in this role may be contingent upon extramural funding and successful performance and may be terminated or reduced in percentage of appointment if such funding is not secured or ceases to be available.
Quick Link
https://careers.msm.edu/postings/23346
EEO Statement Summary
Morehouse School of Medicine is an equal opportunity/equal access/affirmative action employer fully committed to achieving a diverse workforce and complies with all Federal and Georgia State laws, regulations, and executive orders regarding non-discrimination and affirmative action. Morehouse School of Medicine does not discriminate on the basis of race, age, color, religion, national origin or ancestry, sex, gender, disability, veteran status, genetic information, sexual orientation, or gender identity or expression.
Job Duties
Description of Job Duty

Apply