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Clinical Research Program Manager Jobs in Alabama

Alcanza Clinical Research

Research Assistant

Birmingham, AL · On-site

$18 - $24.75/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

The Research Assistant (RA) provides support to the Clinical Research Coordinators (CRCs), Site Manager, Principal and Sub Investigators, and other site staff in compliance with GCP, ICH, HIPAA, FDA ...

Alcanza Clinical Research

Research Assistant

Birmingham, AL · On-site

$18 - $24.75/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

The Research Assistant (RA) provides support to the Clinical Research Coordinators (CRCs), Site Manager, Principal and Sub Investigators, and other site staff in compliance with GCP, ICH, HIPAA, FDA ...

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Showing results 21-40

All JobsClinical Research Program JobsClinical Research Program Manager JobsClinical Research Program Manager Jobs in Alabama

Clinical Research Program Manager information

See Alabama salary details

$40.3K

$83.9K

$135.5K

How much do clinical research program manager jobs pay per year?

As of Aug 18, 2026, the average yearly pay for clinical research program manager in Alabama is $83,934.00, according to ZipRecruiter salary data. Most workers in this role earn between $65,700.00 and $95,200.00 per year, depending on experience, location, and employer.

What does a clinical research program manager do?

A Clinical Research Program Manager oversees the planning, implementation, and management of clinical research studies within an organization. They coordinate research activities, ensure compliance with regulatory requirements, manage budgets, and supervise research staff. Their role is crucial in maintaining timelines, quality standards, and communication among stakeholders, including investigators, sponsors, and regulatory authorities. They also play a key part in developing study protocols and ensuring that research activities align with organizational goals.

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

To thrive as a Clinical Research Program Manager, you need a strong background in clinical research, project management, regulatory compliance, and often an advanced degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and certifications such as CCRP or PMP are typically required. Excellent leadership, organizational, and communication skills set standout managers apart, enabling them to coordinate teams and stakeholders effectively. These skills and qualifications are crucial for ensuring clinical studies meet regulatory standards, stay on schedule, and achieve high-quality outcomes.

What are some typical challenges faced by clinical research program managers in coordinating multi-site studies?

Clinical Research Program Managers often encounter challenges when coordinating multi-site studies, such as ensuring consistent protocol adherence across locations, managing data collection timelines, and addressing site-specific regulatory requirements. Effective communication and strong organizational skills are essential to keep all teams aligned and to resolve issues promptly. Additionally, the role frequently involves collaborating with investigators, sponsors, and regulatory bodies to maintain study integrity and ensure compliance.

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

AspectClinical Research Program ManagerClinical Research Coordinator
CredentialsBachelor's or higher in life sciences, often with project management certificationsTypically holds a bachelor's degree in health sciences or related field
Work EnvironmentOversees multiple studies, manages teams, and coordinates with stakeholdersHandles daily study activities, patient interactions, and data collection
Employer & Industry UsagePharmaceutical companies, CROs, academic institutionsHospitals, clinics, research sites
Search & Comparison IntentFocuses on management, oversight, and program coordinationFocuses on study-specific tasks and patient management

The Clinical Research Program Manager oversees multiple research projects, manages teams, and ensures compliance across studies. In contrast, the Clinical Research Coordinator handles the day-to-day activities of individual studies, including patient interactions and data collection. Both roles require relevant credentials but differ in scope and responsibilities.

What are the most commonly searched types of Clinical Research Program jobs in Alabama?

The most popular types of Clinical Research Program jobs in Alabama are:

What are popular job titles related to Clinical Research Program Manager jobs in Alabama?

For Clinical Research Program Manager jobs in Alabama, the most frequently searched job titles are:

What job categories do people searching Clinical Research Program Manager jobs in Alabama look for?

The top searched job categories for Clinical Research Program Manager jobs in Alabama are:

What cities in Alabama are hiring for Clinical Research Program Manager jobs?

Cities in Alabama with the most Clinical Research Program Manager job openings:

Clinical Research Program Manager jobs near you
Infographic showing various Clinical Research Program Manager job openings in Alabama as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 16% Part Time, and 6% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $83,934 per year, or $40.4 per hour.

MANAGER-CLINICAL RESEARCH NURSING

UAB NOVA RENT

Birmingham, AL • On-site

$85K - $139K/yr

Full-time

Re-posted 17 hours ago

Job description

The University of Alabama at Birmingham (UAB), O'Neal Comprehensive Cancer Center is seeking a Manager-Clinical Research Nursing.
The O'Neal Comprehensive Cancer Center is one of 51 NCI-designated comprehensive cancer centers in the United States and is the only one in Alabama and in the Deep South region. A comprehensive designation also means UAB Medicine patients have access to leading-edge treatments or clinical trials that they may not otherwise have at local community hospitals or smaller cancer centers. For many, an NCI designation can hold the key to survival. On campus and around Birmingham, the O'Neal Cancer Center is a significant part of our economic powerhouse. The O'Neal Cancer Center powers more than 400 scientists and physician-scientists, cares for 20,000 patients annually, and is home to more than 160 employees, plus all the physicians and clinical staff engaged in cancer patient care. The link to our website is: https://www.uab.edu/onealcancercenter/
Please attach a current resume with this application.
General Responsibilities
  • To oversee staff in conducting all study activities including more complex protocols in accordance with the protocol, IRB regulations, and Good Clinical Practice (GCP).
  • To assist with the management of the life cycle of the clinical trial as needed from study start-up through trial maintenance to study closure.
  • To oversee and/or manage multiple clinical research protocols and the associated personnel.
  • To serve as a resource person or act as a subject matter expert (SME) within area of clinical expertise.

Key Duties & Responsibilities
  1. The Manager-Clinical Research Nursing oversees staff in conducting all study activities, including more complex protocols, in accordance with the protocol, IRB regulations, and Good Clinical Practice (GCP). Assists staff in managing the life cycle of the clinical trial as needed from study start-up through trial maintenance to study closure.
  2. Oversees and/or manages multiple clinical research protocols and the associated personnel. Serves as a resource person or acts as a subject matter expert (SME) within the area of clinical expertise.
  3. Creates documents related to patient safety and security. Provides division-wide training in ethical conduct of clinical research.
  4. Trains staff in the use of Electronic Data Capture (EDC) systems and Case Report Forms (CRF). Conducts periodic internal audits of fields in the OnCore CTMS to ensure compliance with institutional requirements. Develops reports and assists unit leadership as needed. Develops standard operating procedures (SOPs) for data quality assurance.
  5. Assists with the development of protocols. Assigns, reviews, and trains staff in study operations. Mentors junior staff. Collaborates with other research units across campus as well as sponsors, investigators, study personnel, participants, health care providers, and Departmental leadership.
  6. Collaborates with administrative personnel to establish financial monitoring systems involving patient care activities. Directs the performance of study audits and monitoring activities to ensure compliance with all clinical regulatory aspects of the research.
  7. Monitors and initiates corrective action to maintain the environment of care, including equipment and material resources. Initiates and/or assists with developing and revising policies and procedures for nursing practice.
  8. Manages project organization, including coordination of internal and external regulations and guidelines affecting clinical research. Designs best practices for management of IP for drug, device, and biologic studies. Creates and evaluates study budgets.
  9. Performs other duties as assigned.

Annual Salary Range : $85,600 - $139,100
Qualifications
Bachelor's degree in a related field and eight (8) years of related experience required. Work experience may NOT substitute for education requirement. Certified Clinical Research Coordinator (CCRC) or Certified Clinical Research Professional (CCRP) certification preferred. Currently licensed as a Registered Nurse (RN) by the Alabama Board of Nursing required.
Preferences
Hard skills: clinical trial, clinical research and data management, protocol compliance management, educating patients and family concerning medical conditions
Soft skills: management, problem-solving, critical thinking, teamwork, organizational, leadership, communication, flexibility, and emotional intelligence.
  • BSN degree.
  • Knowledge of Oncology, clinical research, protocol, and clinical trial management.
  • Generally, may walk approximately one mile a day and lift 5 pounds daily.

UAB is an Equal Employment/Equal Educational Opportunity Institution dedicated to providing equal opportunities and equal access to all individuals regardless of race, color, religion, ethnic or national origin, sex (including pregnancy), genetic information, age, disability, and veteran's status. As required by Title IX, UAB prohibits sex discrimination in any education program or activity that it operates. Individuals may report concerns or questions to UAB's Assistant Vice President and Senior Title IX Coordinator. The Title IX notice of nondiscrimination is located at uab.edu/titleix.

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