Full time
yesterday
R00103615
About Us:
At the forefront of medical discovery as it relates to understanding the causes of obesity, diabetes, cardiovascular disease, cancer and dementia, Pennington Biomedical Research Center is a campus of Louisiana State University and conducts basic, clinical and population research. The Center includes Basic Science, Clinical Research, and Population and Public Health, enabling both focused research and translational science. Research at Pennington Biomedical is supported broadly by multiple NIH Research Centers, and includes approximately 65 faculty and 20 postdoctoral fellows who comprise a network of 44 laboratories and 13 highly specialized core service facilities. Pennington Biomedical is located within state-of-the-art research facilities on a 222-acre campus in Baton Rouge, Louisiana.

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Job Posting Title:
Clinical Research Specialist - Pediatric Clinical Trials
Position Type:
Professional / Unclassified
Department:
LSUPBRC PopSci - Pediatric Obesity and Health Behavior - Project Management (Natalie Malek (00057821))
Work Location:
LSU - Pennington Biomedical
Pay Grade:
Professional
Job Description:
Pennington Biomedical Research Center, a world-renowned academic research institute of Louisiana State University, is seeking a Clinical Research Specialist in the Pediatric Obesity and Health Behavior Laboratory.
The Clinical Research Specialist will conduct clinical trial study visits, including preparation, data collection, and entry. Responsibilities include obtaining informed consent, measuring anthropometrics, assessing diet and activity, and administering questionnaires. This position will be responsible for coordinating data collection and intervention delivery at clinical sites and ensuring high data quality and consistency. Effective communication with participants for scheduling, reminders, screenings, interventions, and follow-ups is essential. Proficiency in REDCap database entry and conducting off-campus procedures as per study protocols is required. Ideal candidates will have a strong educational background, relevant experience, and excellent organizational and communication skills.
Join us to contribute to impactful clinical research and advance healthcare!

REQUIRED QUALIFICATIONS

• As part of a career progression group, vacancy may be filled from this recruitment as a Research Specialist 1 or 2 depending on the level of experience of the selected applicant.

RESEARCH SPECIALIST 2

• Three (3) to five (5) years of experience in a healthcare setting, particularly in pediatric care and clinical research, and/or performing assessments in human subjects.
• Prior experience in clinical research, with a focus on conducting clinical trial visits and data collection. Experience in informed consenting, anthropometrics, body composition measurements, and administering questionnaires is highly desirable.
• Proficiency in using clinical research databases like REDCap for data entry and management is essential. Familiarity with electronic data capture (EDC) systems and other relevant software is also beneficial.
• All additional qualifications as listed above.
  Pennington Biomedical Research Center (PBRC) is an equal employment opportunity employer and serves as a model employer for individuals with disabilities.
  Additional Job Description:
  Flexible schedule required. This position will require some work after regular hours. Intermittent travel is sometimes required when conducting studies inside and outside of Baton Rouge.
  Competencies:
  None
  Special Instructions:
  Interested candidates should include a cover letter and resume to the online application. Official transcripts are required prior to hire and are not required at the time of application.
  Posting Date:
  July 24, 2025
  Closing Date (Open Until Filled if No Date Specified):
  August 7, 2025
  Additional Position Information:
  Pennington Biomedical is located within state-of-the-art research facilities on a 222-acre campus in Baton Rouge, Louisiana. For more information, visit PBRC.
  Questions regarding career opportunities at Pennington Biomedical should be sent to hrm@pbrc.edu.
  Background Check - An offer of employment is contingent on a satisfactory pre-employment background check.
  Benefits - Pennington Biomedical Research Center offers outstanding benefits to eligible employees and their dependents including health, life, dental, and vision insurance; flexible spending accounts; retirement options; various leave options; paid holidays; wellness benefits; tuition exemption for qualified positions; training and development opportunities; employee discounts; and more!
  Positions approved to work outside the State of Louisiana shall be employed through Louisiana State University’s partner, nextSource Workforce Solutions, for Employer of Record Services including but not limited to employment, benefits, payroll, and tax compliance. Positions employed through Employer of Record Services will be offered benefits and retirement as applicable through their provider and will not be eligible for State of Louisiana benefits and retirement.
  Essential Position (Y/N):
  Pennington Biomedical Research Center/LSU is an Equal Opportunity Employer.
  Contact Information:
  Questions or concerns can be directed to PBRC Human Resources at 225-763-2776 or hrm@pbrc.edu

• Conduct Clinical Trial Study Visits: Prepare for and conduct clinical trial study visits, including data collection and entry. Ensure all necessary materials and equipment are ready, accurately collect data during visits, and promptly enter data into the appropriate systems.
• Perform Clinical Research Data Collection Activities: Carry out various clinical research data collection tasks, such as obtaining informed consent from participants, measuring anthropometrics and body composition, assessing diet and physical activity, and administering questionnaires. Ensure all data is collected accurately and in accordance with study protocols.
• Coordinate and Implement Data Collection and Intervention Delivery: Assist in the coordination, implementation, and execution of data collection and intervention delivery at clinical sites. Ensure consistency with established strategies, commitments, and goals to maintain high data quality. Monitor and adjust processes as needed to ensure smooth operation.
• Communicate Effectively with Participants: Maintain clear and effective communication with study participants. This includes scheduling visits, making reminder calls, sending emails, conducting screenings, delivering interventions, and performing follow-ups. Ensure participants are well-informed and supported throughout the study.
• Enter Clinical Trial Data in REDCap Database: Accurately enter clinical trial data into the REDCap database. Ensure data is entered promptly and correctly, following all relevant guidelines and protocols.
• Perform Off-Campus Procedures and Visits: Conduct off-campus procedures and visits as outlined by the study protocol and visit checklists. Ensure all activities are performed in accordance with study requirements and maintain high standards of data collection and participant care.