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Clinical Research Program Manager Jobs in Rochester, MN

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Clinical Research Program Manager information

See Rochester, MN salary details

$43.4K

$90.4K

$146K

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

As of Jun 30, 2026, the average yearly pay for clinical research program manager in Rochester, MN is $90,407.00, according to ZipRecruiter salary data. Most workers in this role earn between $70,800.00 and $102,500.00 per year, depending on experience, location, and employer.

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 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 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 key skills and qualifications needed to thrive as a Clinical Research Program Manager, and why are they important?

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 job categories do people searching Clinical Research Program Manager jobs in Rochester, MN look for? The top searched job categories for Clinical Research Program Manager jobs in Rochester, MN are:
What cities near Rochester, MN are hiring for Clinical Research Program Manager jobs? Cities near Rochester, MN with the most Clinical Research Program Manager job openings:
Clinical Research Program Manager jobs near you

Phlebotomist - Home Visits (Clinical Research, Per Diem)

Hawthorne Health

Rochester, MN • Remote

$17.25 - $21.50/hr

Contractor

Posted 16 days ago

Key responsibilities

  • Conduct in-home visits with clinical trial participants according to study schedules.

  • Perform venipuncture and collect blood specimens following study protocols and safety guidelines.

  • Process, label, and prepare specimens for shipment to central laboratories.

Job description

Job Type: Contract / Per-DiemCompensation: Pay is based on experience and paid on a per-visit basis. Pay for Travel is included. Job Overview

We are seeking a skilled and compassionate Mobile Clinical Research Phlebotomist to support clinical research studies by conducting in-home visits with study participants. In this role, you will perform blood draws, collect biological specimens, and complete study procedures according to clinical research protocols.

This position is ideal for phlebotomists who are comfortable working independently, traveling to patient homes, and providing a professional, patient-centered experience while supporting important clinical research.

Responsibilities

  • Conduct in-home visits with clinical trial participants according to study schedules

  • Perform venipuncture and collect blood specimens following study protocols and safety guidelines

  • Process, label, and prepare specimens for shipment to central laboratories

  • Accurately document study procedures and visit details

  • Maintain compliance with study protocols and Good Clinical Practice (GCP) guidelines

  • Maintain proper chain of custody for biological specimens

  • Ensure participant safety, privacy, and comfort during home visits

  • Communicate with clinical research coordinators and study teams as needed

  • Manage and maintain phlebotomy and specimen collection supplies

  • Follow all infection control and safety procedures

Required Qualifications

  • High school diploma or equivalent

  • Phlebotomy certification from an accredited program

  • Minimum 1–2 years of phlebotomy experience

  • Demonstrated experience performing venipuncture on diverse patient populations

  • Reliable transportation and ability to travel to participant homes

  • Valid driver’s license with a clean driving record

  • Strong interpersonal and communication skills

  • Ability to work independently and manage a flexible schedule

  • Comfortable using electronic documentation systems

Preferred Qualifications

  • Experience working in clinical research or clinical trials

  • Knowledge of clinical trial protocols and documentation requirements

  • Familiarity with specimen processing and shipment procedures

  • Experience providing mobile or home-based healthcare services

  • Certification in Good Clinical Practice (GCP)

Physical Requirements

  • Ability to travel to participant homes within the assigned region

  • Ability to lift and carry specimen kits and medical supplies

  • Ability to stand, bend, and safely perform venipuncture procedures

  • Ability to use a tablet or computer for documentation

Work Environment

  • Home visit setting (travel to participant residences)

  • Collaboration with clinical research teams and study coordinators

  • Flexible scheduling based on participant availability

Required Qualifications
Active BLS (Basic Life Support) certification
Pay is based on experience and paid on a per-visit basis. Pay for travel is included.

We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.To view our privacy policy and terms of use, please use the links below. Privacy Policy: https://hawthornehealth.com/privacy-policy/Terms of Use: https://hawthornehealth.com/terms-of-use/