What are the responsibilities and job description for the Clinical Trial Program Manager position at Pennington Biomedical Research Center?
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.
All Job Postings will close at 12:01a.m. CST (1:01a.m. EST) on the specified Closing Date (if designated). If you close the browser or exit your application prior to submitting, the application progress will be saved as a draft. You will be able to access and complete the application through “My Draft Applications” located on your Candidate Home page. Job Posting Title:Clinical Trial Program ManagerPosition Type:Professional / UnclassifiedDepartment:LSUPBRC Cores - CTU - Project Management Office (Cody VanMeter (00087651) (Inherited))Work Location:LSU - Pennington BiomedicalPay Grade:ProfessionalJob Description:
Pennington Biomedical Research Center , a world-renowned academic research institute of Louisiana State University, is seeking a Program Manager in the Clinical Trials Unit.
The Clinical Trials Program Manager must be motivated to lead and oversee multiple clinical research studies. This role is responsible for managing trial operations, ensuring compliance with regulatory requirements, and driving strategic initiatives to enhance the center’s research impact. As a key member of the research team, the Clinical Trials Program Manager will collaborate with principal investigators and research staff to ensure trials are conducted efficiently, ethically, and in alignment with institutional and federal guidelines. This position offers an exciting opportunity to contribute to groundbreaking research that advances human health while developing innovative clinical trial processes.
Major Responsibilities
Project Planning and Management
Additional Job Description:Competencies:NoneSpecial Instructions:Interested candidates should include a resume and a list of three (3) professional references to the online application. Professional references should be the name, title, company, and contact information from past employers. Professional references should include current or previous supervisors and/or coworkers. Personal references should not be considered for the reference check process. We will respect the request that we not contact a current employer. However, we will need to contact a prior supervisor if such a request is made.
A letter of application/cover letter is recommended but not required. Official transcripts are required prior to hire and are not required at the time of application.Posting Date:March 18, 2025Closing Date (Open Until Filled if No Date Specified):April 1, 2025Additional 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 .
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.
All Job Postings will close at 12:01a.m. CST (1:01a.m. EST) on the specified Closing Date (if designated). If you close the browser or exit your application prior to submitting, the application progress will be saved as a draft. You will be able to access and complete the application through “My Draft Applications” located on your Candidate Home page. Job Posting Title:Clinical Trial Program ManagerPosition Type:Professional / UnclassifiedDepartment:LSUPBRC Cores - CTU - Project Management Office (Cody VanMeter (00087651) (Inherited))Work Location:LSU - Pennington BiomedicalPay Grade:ProfessionalJob Description:
Pennington Biomedical Research Center , a world-renowned academic research institute of Louisiana State University, is seeking a Program Manager in the Clinical Trials Unit.
The Clinical Trials Program Manager must be motivated to lead and oversee multiple clinical research studies. This role is responsible for managing trial operations, ensuring compliance with regulatory requirements, and driving strategic initiatives to enhance the center’s research impact. As a key member of the research team, the Clinical Trials Program Manager will collaborate with principal investigators and research staff to ensure trials are conducted efficiently, ethically, and in alignment with institutional and federal guidelines. This position offers an exciting opportunity to contribute to groundbreaking research that advances human health while developing innovative clinical trial processes.
Major Responsibilities
Project Planning and Management
- Coordinate multiple clinical trials from initiation to completion, ensuring adherence to protocols, timelines, and budgets.
- Develop detailed project plans, including timelines, milestones, and deliverables for multiple clinical trials.
- Define project scope, goals, and success criteria in collaboration with investigators and stakeholders.
- Identify risks, create mitigation plans, and ensure contingency strategies are in place.
- Develop and maintain standard operating procedures (SOPs) for clinical trials.
- Monitor trial adherence to ethical and legal standards.
- Ensure patient safety and data integrity in all studies.
- Develop and optimize workflows to improve efficiency, compliance, and data accuracy.
- Allocate staff and resources effectively to meet project demands while maintaining efficiency.
- Ensure study teams have the necessary tools, training, and support to execute trials successfully.
- Serve as the primary point of contact between investigators, sponsors, regulatory bodies, and research teams.
- Organize and lead project meetings, ensuring alignment between all teams and tracking action items.
- Supervise clinical research coordinators, nurses, and other study personnel. Provide training and mentorship on study protocols, patient interaction, and compliance procedures.
- Bachelor's degree in life sciences, public health, clinical research, healthcare administration, or a related field.
- Minimum of two (2) years of research specific experience such as clinical research coordination.
- Ability to lead cross-functional teams, train staff, and communicate effectively with investigators, sponsors, and regulatory bodies.
- Master’s degree (MPH, MS, MBA) or higher in clinical research, public health, business administration, or a related field.
- Professional certifications such as Project Management Professional (PMP), Certified Clinical Research Professional (CCRP), or Certified Clinical Research Coordinator (CCRC).
- Five (5) or more years of clinical trial management, clinical research coordination, or project management in a research setting.
- Experience in program development, stakeholder engagement, and scaling clinical trial operations.
Additional Job Description:Competencies:NoneSpecial Instructions:Interested candidates should include a resume and a list of three (3) professional references to the online application. Professional references should be the name, title, company, and contact information from past employers. Professional references should include current or previous supervisors and/or coworkers. Personal references should not be considered for the reference check process. We will respect the request that we not contact a current employer. However, we will need to contact a prior supervisor if such a request is made.
A letter of application/cover letter is recommended but not required. Official transcripts are required prior to hire and are not required at the time of application.Posting Date:March 18, 2025Closing Date (Open Until Filled if No Date Specified):April 1, 2025Additional 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 .
