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Manager Clinical Systems Jobs in Raleigh, NC (NOW HIRING)

Connexion Systems & Engineering, Inc.

Be Seen First

Clinical Study Manager

Durham, NC · On-site

$57 - $71/hr

Clinical Study Manager Hiring Organization ... Connexion Systems & Engineering Compensation, Benefits, and Employment Type * Duration: 1+ year ...

Posted today

IQVIA, Inc.

Manager, Clinical Operations

Durham, NC · On-site

$86K - $216K/yr

... systems access and training to complete job responsibilities. Provide oversight for the execution ... Req • Prior clinical trial experience including experience in a management/leadership capacity or ...

IQVIA

Manager, Clinical Operations

Durham, NC

$86K - $216K/yr

Ensure that staff has the proper materials, systems access and training to complete job ... Manage the quality of assigned staff's clinical work through regular review and evaluation of work ...

IQVIA

Manager, Clinical Operations

Durham, NC

$86K - $216K/yr

Ensure that staff has the proper materials, systems access and training to complete job ... Manage the quality of assigned staff's clinical work through regular review and evaluation of work ...

CTI

Clinical Project Coordinator

Raleigh, NC · On-site

Manage and maintain CTI clinical system user account requests * Support the review and tracking of site prescreening, screening, and enrollment activities as well as subject status information ...

System One

Clinical Study Manager

Durham, NC · On-site

Clinical Study Manager Location: Durham, North Carolina Type: 12-month Contract Work Model: Onsite ... System One, and its subsidiaries including Joulé and Mountain Ltd., are leaders in delivering ...

System One

Clinical Study Manager

Durham, NC · On-site

Clinical Study Manager Location: Durham, North Carolina Type: 12-month Contract Work Model: Onsite ... System One, and its subsidiaries including Joulé and Mountain Ltd., are leaders in delivering ...

System One

Clinical Study Manager

Durham, NC · On-site

Clinical Study Manager Location: Durham, North Carolina Type: 12-month Contract Work Model: Onsite ... System One, and its subsidiaries including Joulé and Mountain Ltd., are leaders in delivering ...

System One

Clinical Study Manager

Durham, NC · On-site

Clinical Study Manager Location: Durham, North Carolina Type: 12-month Contract Work Model: Onsite ... System One, and its subsidiaries including Joulé and Mountain Ltd., are leaders in delivering ...

System One

Clinical Study Manager

Durham, NC · On-site

Clinical Study Manager Location: Durham, North Carolina Type: 12-month Contract Work Model: Onsite ... System One, and its subsidiaries including Joulé and Mountain Ltd., are leaders in delivering ...

System One

Clinical Study Manager

Durham, NC · On-site

Clinical Study Manager Location: Durham, North Carolina Type: 12-month Contract Work Model: Onsite ... System One, and its subsidiaries including Joulé and Mountain Ltd., are leaders in delivering ...

Belcan

Clinical Study Manager

Durham, NC

$56.99 - $71.32/hr

Clinical Study Manager Pay Rate: $56.99 - $71.32/hr. Location: Durham, NC ZIP Code: 27701 Start ... Experience using clinical systems and tools such as CTMS, eTMF, EDC, Microsoft Office, and study ...

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All JobsClinical Systems JobsManager Clinical Systems JobsManager Clinical Systems Jobs in Raleigh, NC

Manager Clinical Systems information

See Raleigh, NC salary details

$44.7K

$99.2K

$148.7K

How much do manager clinical systems jobs pay per year?

As of Jul 15, 2026, the average yearly pay for manager clinical systems in Raleigh, NC is $99,217.00, according to ZipRecruiter salary data. Most workers in this role earn between $74,800.00 and $121,500.00 per year, depending on experience, location, and employer.

What is the difference between Manager Clinical Systems vs Clinical Systems Coordinator?

AspectManager Clinical SystemsClinical Systems Coordinator
CredentialsBachelor's degree in healthcare, IT, or related field; certifications in clinical systems or project managementAssociate's or Bachelor's degree; familiarity with clinical systems and healthcare workflows
Work EnvironmentOversees clinical IT teams, collaborates with healthcare providers, manages system implementationsSupports clinical system operations, assists in training, troubleshoots user issues
Employer & Industry UsageHospitals, healthcare systems, clinicsHospitals, clinics, healthcare organizations
Search & Comparison IntentHigh overlap in responsibilities and credentials, often compared for career progressionRelated role focusing on support and coordination

The main difference is that the Manager Clinical Systems oversees the entire clinical systems team and manages implementations, while the Clinical Systems Coordinator provides support, training, and troubleshooting assistance within the clinical IT environment.

What are the key skills and qualifications needed to thrive as a Manager Clinical Systems, and why are they important?

To thrive as a Manager Clinical Systems, you need expertise in healthcare informatics, project management, and clinical workflow analysis, typically supported by a relevant degree and experience in a clinical or IT environment. Familiarity with electronic health records (EHR) platforms, HL7 standards, and certifications like PMP or Certified Professional in Healthcare Information and Management Systems (CPHIMS) are often required. Strong leadership, communication, and problem-solving skills are crucial for effectively guiding teams and liaising between clinical and technical stakeholders. These abilities ensure the successful implementation and optimization of clinical systems, leading to improved patient outcomes and operational efficiency.

Is being a MOA a good entry level job?

Medical Office Assistants (MOAs) often serve as entry-level healthcare support roles, providing administrative and clinical assistance in medical settings. It can be a good starting point for those interested in healthcare careers, offering experience with medical procedures, patient interaction, and office management. However, advancement may require additional certifications or education depending on career goals.

What are the common challenges faced by a Manager Clinical Systems when implementing new healthcare technology solutions?

A Manager Clinical Systems often encounters challenges such as ensuring seamless integration of new technology with existing electronic health records (EHRs), managing change resistance among clinical staff, and maintaining compliance with healthcare regulations. Balancing the differing needs of IT and clinical teams while keeping patient safety and data security as top priorities can also be complex. Effective communication, stakeholder engagement, and thorough user training are key strategies for overcoming these obstacles and ensuring successful technology adoption.

What does a clinical systems manager do?

A clinical systems manager oversees the implementation, maintenance, and optimization of electronic health record (EHR) systems and other clinical software. They coordinate between healthcare providers and IT teams, ensure compliance with healthcare regulations, and often require knowledge of healthcare workflows, IT skills, and certifications such as Epic or Cerner system training.

What does a clinical manager do?

A clinical manager oversees healthcare operations within a clinical setting, such as hospitals or clinics. They coordinate staff, ensure compliance with healthcare regulations, manage budgets, and implement policies to improve patient care quality. Strong leadership, communication skills, and knowledge of healthcare systems are essential for this role.

What is the highest paying job in healthcare management?

In healthcare management, the highest paying roles are typically executive positions such as Chief Executive Officer (CEO) or Chief Operating Officer (COO) of healthcare organizations, with salaries often exceeding $200,000 annually. These roles require extensive experience, leadership skills, and often advanced degrees like an MBA or healthcare administration certification.

What does a Manager Clinical Systems do?

A Manager Clinical Systems oversees the implementation, maintenance, and optimization of clinical information systems within a healthcare organization. They ensure that electronic health records and other clinical technologies support efficient, accurate, and secure patient care. This role involves collaborating with IT teams, clinicians, and administrators to align system functionality with clinical workflows. Managers also lead projects, manage staff, and ensure systems comply with healthcare regulations such as HIPAA.
What are popular job titles related to Manager Clinical Systems jobs in Raleigh, NC? For Manager Clinical Systems jobs in Raleigh, NC, the most frequently searched job titles are:
What job categories do people searching Manager Clinical Systems jobs in Raleigh, NC look for? The top searched job categories for Manager Clinical Systems jobs in Raleigh, NC are:
What cities near Raleigh, NC are hiring for Manager Clinical Systems jobs? Cities near Raleigh, NC with the most Manager Clinical Systems job openings:
Manager Clinical Systems jobs near you
Clinical Study Manager

Clinical Study Manager

Connexion Systems & Engineering, Inc.

Durham, NC • On-site

$57 - $71/hr

Contractor

Medical, Dental

Posted 22 hours ago

Posted today

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Job description

Title: Clinical Study Manager
Hiring Organization: Connexion Systems & Engineering
Compensation, Benefits, and Employment Type

  • Duration: 1+ year contract, possible extension
  • Pay rate: $56.99–$71.32/hour
  • Job Location: Durham, NC
  • Schedule: Monday–Friday, 8:00 AM–5:00 PM
  • Job#: bh19291


Description:
We are seeking an experienced Clinical Study Manager to lead the operational execution of clinical studies from start-up through close-out. This position is responsible for coordinating study activities, managing CROs and vendors, overseeing timelines, and ensuring studies are conducted in compliance with ICH/GCP guidelines, regulatory requirements, and established SOPs.
The ideal candidate is an organized clinical operations professional with strong project management skills and experience working in a sponsor environment.
Responsibilities

  • Manage day-to-day clinical study operations from study start-up through close-out.
  • Coordinate activities with cross-functional teams, CROs, vendors, investigators, and clinical sites.
  • Track study timelines, milestones, deliverables, and operational risks.
  • Lead or support study team, vendor, and CRO meetings.
  • Oversee site activation, essential document collection, and clinical supply readiness.
  • Monitor vendor and CRO performance while driving issue resolution and corrective actions.
  • Coordinate study-specific training for internal and external stakeholders.
  • Maintain Trial Master File (TMF) quality, reconciliation, and inspection readiness.
  • Review and approve study documentation, including informed consent forms, monitoring plans, laboratory manuals, and other essential study documents.
  • Support audit readiness and regulatory compliance throughout the study lifecycle.
  • Oversee CTMS reporting and study tracking activities.
  • Review clinical data, monitoring reports, and vendor deliverables to support data integrity.
  • Collaborate with Data Management, Safety, Regulatory Affairs, Clinical Supplies, Biostatistics, Contracts, and other functional groups.
  • Assist with study budgets, vendor scopes of work, invoice review, and financial tracking.


Qualifications
Required

  • Bachelor's degree in Life Sciences, Health Sciences, or a related field (or equivalent experience).
  • Minimum of 8 years of clinical research experience.
  • At least 2 years of Clinical Study Management, Clinical Operations, or related sponsor-side experience.
  • Experience managing CROs, vendors, clinical sites, and cross-functional study teams.
  • Strong knowledge of:
    • ICH/GCP guidelines
    • Clinical trial operations
    • Regulatory requirements
    • Study start-up through close-out activities
  • Experience using CTMS, eTMF, EDC, Microsoft Office, and related clinical systems.
  • Excellent organizational, communication, and project management skills.


Preferred

  • Sponsor-side clinical study management experience.
  • Trial Master File (TMF) oversight.
  • Audit and inspection readiness experience.
  • Vendor oversight and performance management.
  • Budget management and financial tracking experience.


Ideal Candidate
We're looking for a proactive clinical operations professional who thrives in a collaborative environment and can successfully manage multiple priorities while maintaining compliance, quality, and study timelines. Strong leadership, problem-solving, and communication skills are essential.
Apply today to join a collaborative team supporting the successful execution of impactful clinical research studies.