ZipRecruiter

Log In

1

Clinical Research Program Manager Jobs in Alabama

previous page

Showing results 41-60

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 17, 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.

CLINICAL RESEARCH ADMINISTRATOR III (3)

UAB NOVA RENT

Birmingham, AL • On-site

$55K - $89K/yr

Full-time

Re-posted 9 days ago

Job description

The University of Alabama at Birmingham (UAB), O'Neal Comprehensive Cancer Center, is seeking a Clinical Research Administrator III.
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 act as a resource for faculty and staff regarding administrative duties for industry and sponsored clinical research.
  • To serve as an informational and referral resource for the clinical research community.
  • To work with necessary parties to identify compliance, legal, IP and business/financial risk.
  • To manage accounts across all studies as needed.
  • To process and analyze reports in OnCore, as needed.

Key Duties & Responsibilities
  1. Acts as a resource for faculty and staff regarding administrative duties for industry and sponsored clinical research.
  2. Serves as an informational and referral resource for the clinical research community.
  3. Works with necessary parties to identify compliance, legal, IP and business/financial risk.
  4. Manages accounts across all studies as needed.
  5. Conducts literature reviews. Assesses and determines solutions for operational shortcomings of protocols. Determines operational elements needed for conduct of clinical studies.
  6. Trains staff in various work responsibilities, as needed. Provides training to office personnel in ethical conduct of research. Contributes to strategic planning within the respective Department or School, as needed.
  7. Maintains currency in field through cross training, continuing education, literature and seminars in order to implement this knowledge and create efficiencies within the Department.
  8. Processes and analyzes reports in OnCore, as needed.
  9. Reviews protocol, ICF, Sponsors budget and any other study documents required to build initial calendar
  10. Completes RedCap submission to FAP.
  11. This also includes submission to CCTS and Tissue Procurement Submissions.
  12. Reviews protocol amendments as they occur and makes any necessary changes to billing plan, then resubmits back to FAP.
  13. Ancillary Department Submissions (i.e. Radiology, CCTS, Tissue Procurement).
  14. Onboarding/training new FAP submitters.
  15. Review of studies with clinical research coordinators
  16. Performs other duties as assigned.

Annual Salary Range : $55,180 - $89,670
Qualifications
Bachelor's degree in a related field and five (5) 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.
Preferences
The ideal candidate must be able to effectively interface professionally between Principal Investigators, Study Coordinators, Regulatory Managers, Financial Associates, Grants and Contracts Officers, Clinical Billing Review Officers, Ancillary Departments, and Sponsors regarding clinical trial activities relating to budgets and contracts to assure Cancer Center investigators' needs are achieved and goals accomplished. Full understanding of the Fiscal Approval Process (FAP)
KSA: Problem-solving skills, working knowledge of related scientific and clinical terminology, Leadership skills, Presentation skills, Prioritization skills, Organizational skills, Written and verbal communication skills.
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.

Apply