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Clinical Research Program Manager Jobs in Montevallo, AL

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Clinical Research Program Manager information

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$43.8K

$91.1K

$147.1K

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

As of Sep 3, 2026, the average yearly pay for clinical research program manager in Montevallo, AL is $91,090.00, according to ZipRecruiter salary data. Most workers in this role earn between $71,300.00 and $103,300.00 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 job categories do people searching Clinical Research Program Manager jobs in Montevallo, AL look for?

The top searched job categories for Clinical Research Program Manager jobs in Montevallo, AL are:

What cities near Montevallo, AL are hiring for Clinical Research Program Manager jobs?

Cities near Montevallo, AL with the most Clinical Research Program Manager job openings:

Clinical Research Program Manager jobs near you

CLINICAL RESEARCH COORDINATOR III

UAB NOVA RENT

Birmingham, AL • On-site

$60K - $98K/yr

Full-time

This job post has expired 1 day ago. Applications are no longer accepted.

Job description

The University of Alabama at Birmingham (UAB), O'Neal Comprehensive Cancer Center, is seeking a Clinical Research Coordinator III. The Clinical Research Coordinator III serves as the primary coordinator for interventional trials and supports more senior team members.
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 serve as a lead coordinator by providing oversight to less experienced staff to ensure quality and regulatory compliance with clinical research operations.
  • To coordinate and manage the research study lifecycle from start-up through close-out.
  • To coordinate and conduct all applicable clinical and administrative activities required by the protocol such as screening, scheduling, consenting, assessing, ordering, collecting, documenting and shipping under the auspices of Good Clinical Practice (GCP).

Key Duties & Responsibilities
  1. Provides a lead role in protocol screening and participant eligibility determination working alongside other team members to ensure compliance.
  2. Provides oversight to clinical research coordinators (CRC) I and IIs and clinical research nurse coordinators (CRNC) I and IIs in review of study start up, SIV planning, subject management, data query resolution and source document development including review of study documents including but not limited to flowsheets, pharmacy orders, labs, and adverse events.
  3. Communicates effectively with CRC and CRNC regarding lab reports and adverse events to ensure protocol compliance with dosing.
  4. In conjunction with PI or Director, interprets and applies current research findings in area of clinical specialty and reports findings in professional journals and local, state, and national conferences.
  5. Schedules/coordinates patient visits and procedures and tracks the study participant calendar per protocol schedule of events.
  6. Coordinates patient care and/or patient follow-up functions of the clinical study including planning and developing related activities.
  7. Arranges access to study medications, including authorization for prescriptions.
  8. Employs strategies to maintain recruitment and retention rates. In collaboration with the CTO regulatory team and coordinators, completes and submits Adverse Event (AE) and Serious Adverse Event (SAE) reports in a timely manner and in compliance with FDA, sponsor, and institutional policies.
  9. May perform a variety of medical procedures.
  10. Completes OnCore worksheet to ensure proper protocol billing.
  11. Performs the informed consent process following GCP.
  12. Performs other duties as assigned.

Annual Salary Range : $60,835 - $98,855
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
  • Clinical research experience.
  • Ability to lead others in the coordination of research activities involved in conducting Oncology clinical trials.
  • Knowledge of clinical research regulatory/compliance affairs.
  • Problem-solving skills.
  • Working knowledge of related scientific and clinical terminology.
  • Leadership skills.
  • Presentation skills.
  • Prioritization skills.
  • Organizational skills.
  • Written and verbal communication skills.
  • Ability to walk minimally one mile a day and lift 5 - 10 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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