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How much do cancer research manager jobs pay per year?

As of Aug 23, 2026, the average yearly pay for cancer research manager in Mobile, AL is $74,982.00, according to ZipRecruiter salary data. Most workers in this role earn between $54,800.00 and $87,100.00 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 Mobile, AL?

For Cancer Research Manager jobs in Mobile, AL, the most frequently searched job titles are:

What job categories do people searching Cancer Research Manager jobs in Mobile, AL look for?

The top searched job categories for Cancer Research Manager jobs in Mobile, AL are:

Cancer Research Manager jobs near you
Infographic showing various Cancer Research Manager job openings in Mobile, AL as of August 2026, with employment types broken down into 85% Full Time, 9% Part Time, and 6% Contract. Highlights an 94% In-person, 2% Hybrid, and 4% Remote job distribution, with an average salary of $84,001 per year, or $40.4 per hour.

Clinical Research Coordinator (CRC) / RN Clinical Research Coordinator

The US Oncology Network

Mobile, AL • On-site

$20 - $26.50/hr

Full-time

Re-posted 2 days ago

US Oncology rating

7.1

Company rating: 7.1 out of 10

Based on 109 frontline employees who took The Breakroom Quiz

382nd of 891 rated healthcare providers

Job description

Overview

Southern Cancer Center – Springhill Location

Join Our Team!

Southern Cancer Center is seeking a highly organized, detail-oriented, and compassionate Clinical Research Coordinator to join our growing team. This role is critical to advancing cancer care through clinical research by coordinating patient participation in clinical trials and ensuring compliance with study protocols, regulatory requirements, and quality standards.

 
Southern Cancer Center welcomes applications from both Clinical Research Coordinators and Registered Nurses. Qualified RN candidates may be considered for placement in an RN Clinical Research Coordinator role based on education, licensure, and relevant experience.
 

If you are passionate about improving patient outcomes, enjoy working collaboratively with physicians and research teams, and thrive in a fast-paced healthcare environment, we encourage you to apply.

Position Summary

The Clinical Research Coordinator is responsible for coordinating and managing clinical trial activities, including patient screening, enrollment, data collection, regulatory compliance, and ongoing patient monitoring. This individual works closely with physicians, research sponsors, patients, and other healthcare professionals to ensure successful execution of clinical research studies.


Responsibilities
Essential Duties & ResponsibilitiesPatient Recruitment & Clinical Trial Coordination
  • Screen potential patients for protocol eligibility.
  • Present clinical trial opportunities and study details to patients and families.
  • Participate in the informed consent process and enroll eligible patients into clinical trials.
  • Assist with patient care activities required by study protocols.
  • Monitor patient participation and ensure protocol compliance throughout the study.
Clinical Research Activities
  • Collect, enter, and report study data accurately and timely.
  • In collaboration with physicians, review patients for:
    • Changes in condition
    • Adverse events
    • Concomitant medication use
    • Protocol compliance
    • Response to study treatment
  • Thoroughly document all research-related activities and findings.
  • Maintain accurate and complete study records.
Investigational Drug Management
  • May dispense investigational medications in accordance with protocol requirements.
  • Maintain investigational drug accountability and documentation.
Regulatory & Compliance Responsibilities
  • Assist in the collection, preparation, and maintenance of regulatory documents.
  • Ensure compliance with US Oncology Research (USOR) Standard Operating Procedures (SOPs), FDA regulations, and Good Clinical Practice (GCP) guidelines.
  • Participate in monitoring visits, audits, and quality assurance activities.
  • Schedule and coordinate sponsor monitoring and auditing visits as needed.
  • Serve as a liaison with study sponsors, monitors, and auditors.
Laboratory & Specimen Management
  • Assist with collection, preparation, packaging, and shipment of laboratory specimens to central laboratories and vendors.
  • Complete Hazmat and/or IATA training as required.
Professional Development
  • Participate in mandatory training, continuing education, and research-related learning opportunities.
  • Stay current on clinical research regulations, protocols, and best practices.

Qualifications
QualificationsEducation
  • Associate degree in a clinical, scientific, or healthcare-related field required.
  • Bachelor's degree preferred.
Experience
  • Minimum of one (1) year of experience in a clinical or scientific healthcare setting required.
  • Oncology experience strongly preferred.
  • Experience working directly with physicians preferred.
  • Proficiency in Microsoft Office applications required.
Knowledge, Skills & Abilities
  • Excellent verbal and written communication skills.
  • Strong organizational and prioritization skills.
  • Ability to manage multiple tasks and deadlines simultaneously.
  • Exceptional time management skills.
  • Strong interpersonal skills with the ability to work effectively across all levels of the organization.
  • High degree of accuracy and attention to detail.
  • Ability to work independently and collaboratively in a fast-paced environment.
  • Ability to maintain patient confidentiality and professionalism.
  • May be responsible for performing basic clinical assessments.
Why Join Southern Cancer Center?

At Southern Cancer Center, our mission is to provide compassionate, high-quality cancer care while advancing treatment options through innovative clinical research. As a member of our team, you will have the opportunity to make a meaningful impact on patients' lives while contributing to the future of oncology care.

Working ConditionsWork Environment
  • Traditional clinical and office environment.
  • Frequent exposure to conditions common in an oncology/hematology practice, including communicable diseases, toxic substances, ionizing radiation, and medical preparations.
  • Reasonable accommodations may be made to enable qualified individuals with disabilities to perform essential job functions.
Physical Requirements
  • Significant computer-based work.
  • Frequent standing and walking throughout the clinic.
  • Occasional lifting and carrying of items up to 40 pounds.
  • Requires corrected vision and hearing within normal ranges.
Apply Today

Become part of a team dedicated to advancing cancer treatment and improving the lives of our patients through exceptional care and innovative research.

Southern Cancer Center is an Equal Opportunity Employer.

Qualifications:QualificationsEducation
  • Associate degree in a clinical, scientific, or healthcare-related field required.
  • Bachelor's degree preferred.
Experience
  • Minimum of one (1) year of experience in a clinical or scientific healthcare setting required.
  • Oncology experience strongly preferred.
  • Experience working directly with physicians preferred.
  • Proficiency in Microsoft Office applications required.
Knowledge, Skills & Abilities
  • Excellent verbal and written communication skills.
  • Strong organizational and prioritization skills.
  • Ability to manage multiple tasks and deadlines simultaneously.
  • Exceptional time management skills.
  • Strong interpersonal skills with the ability to work effectively across all levels of the organization.
  • High degree of accuracy and attention to detail.
  • Ability to work independently and collaboratively in a fast-paced environment.
  • Ability to maintain patient confidentiality and professionalism.
  • May be responsible for performing basic clinical assessments.
Why Join Southern Cancer Center?

At Southern Cancer Center, our mission is to provide compassionate, high-quality cancer care while advancing treatment options through innovative clinical research. As a member of our team, you will have the opportunity to make a meaningful impact on patients' lives while contributing to the future of oncology care.

Working ConditionsWork Environment
  • Traditional clinical and office environment.
  • Frequent exposure to conditions common in an oncology/hematology practice, including communicable diseases, toxic substances, ionizing radiation, and medical preparations.
  • Reasonable accommodations may be made to enable qualified individuals with disabilities to perform essential job functions.
Physical Requirements
  • Significant computer-based work.
  • Frequent standing and walking throughout the clinic.
  • Occasional lifting and carrying of items up to 40 pounds.
  • Requires corrected vision and hearing within normal ranges.
Apply Today

Become part of a team dedicated to advancing cancer treatment and improving the lives of our patients through exceptional care and innovative research.

Southern Cancer Center is an Equal Opportunity Employer.

Education:UNAVAILABLEEmployment Type: FULL_TIME

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