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Cancer Research Manager Jobs in Baton Rouge, LA (NOW HIRING)

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Cancer Research Manager information

See Baton Rouge, LA salary details

$48K

$94.7K

$166.6K

How much do cancer research manager jobs pay per year?

As of Aug 30, 2026, the average yearly pay for cancer research manager in Baton Rouge, LA is $94,650.00, according to ZipRecruiter salary data. Most workers in this role earn between $69,100.00 and $109,900.00 per year, depending on experience, location, and employer.

What does a cancer research manager do?

A Cancer Research Manager oversees and coordinates cancer research projects, managing teams of scientists and clinicians to ensure studies are conducted efficiently and ethically. They are responsible for developing research protocols, securing funding, ensuring regulatory compliance, and analyzing data. In addition to administrative duties, they often collaborate with other institutions, present findings, and help translate research discoveries into clinical applications that can benefit patients.

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

To thrive as a Cancer Research Manager, you need advanced knowledge of oncology research, project management expertise, and typically a graduate degree in life sciences or a related field. Familiarity with research protocols, clinical trial management systems, regulatory compliance, and certifications such as Good Clinical Practice (GCP) are essential. Strong leadership, problem-solving abilities, and excellent communication skills help manage research teams and collaborate with stakeholders. These skills ensure effective oversight of complex research projects, regulatory adherence, and advancement of cancer research initiatives.

What are the main challenges a cancer research manager faces when coordinating multidisciplinary research teams?

As a Cancer Research Manager, coordinating multidisciplinary teams involves balancing diverse expertise and ensuring effective communication across various scientific domains, such as biology, clinical research, and data analysis. Challenges often include aligning different research methodologies, managing timelines, and integrating findings from multiple projects. Successful managers foster collaboration by setting clear goals, facilitating regular updates, and addressing any conflicts promptly, which helps keep research projects on track and promotes innovative solutions to complex cancer-related questions.

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

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

What job categories do people searching Cancer Research Manager jobs in Baton Rouge, LA look for?

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

Cancer Research Manager jobs near you
Infographic showing various Cancer Research Manager job openings in Baton Rouge, LA as of August 2026, with employment types broken down into 72% Full Time, and 28% Contract. Highlights an 100% In-person job distribution, with an average salary of $94,650 per year, or $45.5 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 13 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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