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Clinical Research Manager Jobs in Baton Rouge, LA

Louisiana State University

Transient

Baton Rouge, LA · On-site

The Center includes Basic Science, Clinical Research, and Population and Public Health, enabling ... Resource Management at hrm@pbrc.edu. COVID-19 Vaccine Protocol: Pennington requires the COVID-19 ...

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Clinical Research Manager information

See Baton Rouge, LA salary details

$47.1K

$103.1K

$181.5K

How much do clinical research manager jobs pay per year?

As of Sep 1, 2026, the average yearly pay for clinical research manager in Baton Rouge, LA is $103,068.00, according to ZipRecruiter salary data. Most workers in this role earn between $77,800.00 and $117,600.00 per year, depending on experience, location, and employer.

What does a clinical research manager do?

A clinical research manager oversees clinical trials, which involve testing new medications or medical devices. Their responsibilities include ensuring all ethical practices and legal protocols are followed and that all paperwork is filled out completely and accurately. They also maintain standards for the data collection and procedures during the clinical trial and make sure all team members, including the doctors and nurses on the trial, are kept informed.

What are the key skills and qualifications needed to thrive as a clinical research manager?

To thrive as a Clinical Research Manager, you need a solid understanding of clinical trial protocols, regulatory requirements (such as GCP), and a background in life sciences or healthcare, often supported by a relevant degree. Familiarity with clinical trial management systems (CTMS), EDC software, and certifications like ACRP or SOCRA are typically expected. Strong leadership, excellent organizational skills, and effective communication abilities set outstanding managers apart. These competencies are critical for ensuring compliance, data integrity, and the successful coordination of multidisciplinary research teams.

What are some common challenges clinical research managers face when overseeing multiple clinical trials simultaneously?

Clinical Research Managers often encounter challenges such as balancing competing timelines, ensuring regulatory compliance across different studies, and effectively allocating resources among projects. Managing communication between diverse teams—such as investigators, sponsors, and regulatory bodies—can also be demanding, especially when trials are at different stages. Developing strong organizational skills and leveraging project management tools are key to successfully navigating these complexities and maintaining high standards for data quality and participant safety.

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

AspectClinical Research ManagerClinical Research Coordinator
CredentialsBachelor's or higher in life sciences, often with experience in project managementBachelor's in health sciences or related field, often with certification like CCRP
Work EnvironmentOversees multiple studies, manages teams, and ensures compliance at a higher levelAssists with daily study activities, patient interactions, and data collection
Employer & Industry UsagePharmaceutical companies, CROs, academic institutionsHospitals, clinics, research sites

The Clinical Research Manager focuses on overseeing entire studies and managing teams, while the Clinical Research Coordinator handles daily study tasks and participant interactions. Both roles require relevant certifications and are essential in clinical research settings, but they differ in scope and responsibilities.

More about Clinical Research Manager jobs

What are the most commonly searched types of Clinical Research jobs in Baton Rouge, LA?

The most popular types of Clinical Research jobs in Baton Rouge, LA are:

What are popular job titles related to Clinical Research Manager jobs in Baton Rouge, LA?

For Clinical Research Manager jobs in Baton Rouge, LA, the most frequently searched job titles are:

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The top searched job categories for Clinical Research Manager jobs in Baton Rouge, LA are:

What cities near Baton Rouge, LA are hiring for Clinical Research Manager jobs?

Cities near Baton Rouge, LA with the most Clinical Research Manager job openings:

Clinical Research Manager jobs near you
Infographic showing various Clinical Research Manager job openings in Baton Rouge, LA as of August 2026, with employment types broken down into 87% Full Time, 12% Part Time, and 1% Contract. Highlights an 83% Physical, 2% Hybrid, and 15% Remote job distribution, with an average salary of $103,068 per year, or $49.6 per hour.

Clinical Research Data & Regulatory Coordinator

Mary Bird Perkins Cancer Center

Baton Rouge, LA • On-site

$23.25 - $31/hr

Full-time

Re-posted 14 days ago

Mary Bird Perkins Cancer Center rating

7.6

Company rating: 7.6 out of 10

Based on 5 frontline employees who took The Breakroom Quiz

Job description

Mary Bird Perkins Cancer Center is Louisiana's leading cancer care organization, caring for more patients each year than any other facility in the region. And with strategic hospital and physician partnerships, we are delivering on our mission to improve survivorship and lessen the burden of cancer.

Mary Bird Perkins and its partners work together to provide state-of-the-art treatments and unparalleled collaborative, comprehensive cancer services. This culture of innovation helps attract the best cancer minds in the country, from expert physicians and highly specialized scientists to forward-thinking leaders in supportive care and other disciplines.

Together, with our hospital and physician partners, we are one-hundred percent focused on cancer care.

Why Join Us? We are looking for talented and highly-motivated individuals who demonstrate a natural desire to support the meaningful work of community oncologists and the patients we serve.

Job Description:

100% IN PERSON POSITION

SCOPE:The Data and Regulatory Coordinator collaborates with the Clinical Research team and the Principal Investigator by knowledge of current protocol requirements; maintains IRB documents, regulatory and protocol documentation for assigned clinical trials administered by the Center which may include multi-site trials; facilitates communication and correspondence between Clinical Research and sponsoring agencies; collects protocol specific information from physicians, nurses, patients, family members, local caregivers, and others utilizing protocol specific methods; ensures that all designated Clinical Research regulatory and data management activities for all clinical research sites are executed in accordance with all applicable laws, regulations, policies and protocol requirements; performs additional duties as requested by supervisor and/or described in position description.

ESSENTIAL FUNCTIONS:

1. Demonstrates knowledge and understanding of the evolution of clinical research.

2. Participates in clinical research studies by assuring that the regulatory and data for trials being managed according to rules and guidelines governing the conduct of clinical research trials.

3. Monitor/Auditor Preparation and Participation

4. IRB Preparation and Presentation

5. Protocol research document maintenance

6. Policies & procedures

7. Other duties and professional development

QUALIFICATIONS:

  • Bachelor's degree or equivalent work experience, preferably in a scientific or technical discipline.

  • Basic science degree, or certification or licensure in a health care field

  • Demonstrated success in management of regulatory submissions activities.

  • Medical or scientific research experience preferred.

  • Professional Certifications preferred

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