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Clinical Study Startup Manager Jobs in Raleigh, NC

Medium

Site Network Manager (North America)

Durham, NC · On-site

$97.50 - $163/hr

Strong understanding of the clinical trial lifecycle , including site feasibility, study startup, patient recruitment, and ICH‑GCP/regulatory requirements. * Excellent relationship management ...

Duke University

Clinical Research Coordinator

Durham, NC

$23.50 - $31.25/hr

Clinical Research Coordinator - Neurosurgery Research Be You. At Duke, we celebrate individuality ... Support study startup, feasibility assessments, ongoing project management, and study closeout ...

Duke University

Clinical Research Coordinator

Durham, NC · On-site

$23.50 - $31.25/hr

Clinical Research Coordinator - Neurosurgery Research Be You. At Duke, we celebrate individuality ... Support study startup, feasibility assessments, ongoing project management, and study closeout ...

Aerogen Ltd

Clinical Trial Manager

Morrisville, NC · On-site

The Clinical Trial Manager (CTM) is responsible for managing various aspects of clinical trials including study start-up, site management and monitoring activities. This includes vendor management ...

Pluto Health

Clinical Project Manager

Durham, NC · On-site

$85K - $120K/yr

Whether it involves preventive health care, at-home tests, or access to lifesaving clinical studies ... As a Clinical Project Manager, you will play a critical role in leading cross-functional teams ...

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Clinical Study Startup Manager information

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How much do clinical study startup manager jobs pay per hour?

As of Aug 18, 2026, the average hourly pay for clinical study startup manager in Raleigh, NC is $60.77, according to ZipRecruiter salary data. Most workers in this role earn between $49.33 and $68.46 per hour, depending on experience, location, and employer.

What does a clinical study startup manager do?

A Clinical Study Startup Manager oversees the initial phases of clinical trials, ensuring all regulatory, ethical, and site-specific requirements are met before a study begins. They coordinate activities such as site selection, contract negotiation, budget management, and regulatory submissions. Their goal is to streamline the startup process to minimize delays and ensure compliance with industry standards, facilitating a smooth transition to patient enrollment and study execution.

What are the key skills and qualifications needed to thrive as a clinical study startup manager?

A Clinical Study Startup Manager requires expertise in clinical research processes, regulatory compliance, and project management, often supported by a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), regulatory submission platforms, and Good Clinical Practice (GCP) certification is typically expected. Strong organizational, communication, and stakeholder management skills help facilitate collaboration and timely study initiation. These skills ensure smooth, compliant, and efficient study startup, which is critical for the overall success and timelines of clinical trials.

What are some common challenges faced by clinical study startup managers during the site activation process?

Clinical Study Startup Managers often encounter challenges such as varying regulatory requirements across regions, delays in site contract negotiations, and managing the collection of essential documents from multiple stakeholders. Coordinating with cross-functional teams—including regulatory affairs, legal, and clinical operations—requires strong project management and communication skills to keep timelines on track. Anticipating potential bottlenecks and proactively addressing site-specific concerns are critical for ensuring a smooth and timely study startup.

What is the difference between Clinical Study Startup Manager vs Clinical Research Coordinator?

AspectClinical Study Startup ManagerClinical Research Coordinator
ResponsibilitiesOversees study initiation, site selection, regulatory submissions, and startup activitiesManages participant recruitment, data collection, and day-to-day study operations at sites
Required CredentialsBachelor's degree, clinical research experience, knowledge of regulationsBachelor's degree, clinical research experience, good clinical practice (GCP) training
Work EnvironmentCorporate or sponsor offices, clinical trial sitesClinical trial sites, hospitals, research centers

The Clinical Study Startup Manager focuses on preparing and initiating clinical trials, ensuring regulatory compliance and site readiness. In contrast, the Clinical Research Coordinator handles the daily operations at trial sites, managing participant interactions and data collection. Both roles require similar credentials and work in related environments, but their core responsibilities differ significantly.

What are the most commonly searched types of Clinical Study Startup jobs in Raleigh, NC?

The most popular types of Clinical Study Startup jobs in Raleigh, NC are:

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For Clinical Study Startup Manager jobs in Raleigh, NC, the most frequently searched job titles are:

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The top searched job categories for Clinical Study Startup Manager jobs in Raleigh, NC are:

What cities near Raleigh, NC are hiring for Clinical Study Startup Manager jobs?

Cities near Raleigh, NC with the most Clinical Study Startup Manager job openings:

Clinical Study Startup Manager jobs near you
Infographic showing various Clinical Study Startup Manager job openings in Raleigh, NC as of August 2026, with employment types broken down into 86% Full Time, 12% Part Time, and 2% Contract. Highlights an 83% Physical, 2% Hybrid, and 15% Remote job distribution, with an average salary of $126,404 per year, or $60.8 per hour.

Site Network Manager (North America)

Medium

Durham, NC • On-site

$97.50 - $163/hr

Other

This job post has expired today. Applications are no longer accepted.

Job description

The Alimentiv Site Network Manager will be responsible to drive and deliver on the Alimentiv Site Network (ASN) Strategy. This position will drive the project management, process optimization and growth of the ASN globally through identification, outreach, collaboration with and onboarding of clinical sites with a focus on enhancing clinical trial delivery.

This position will be responsible for developing and driving key performance indicators around the success of ASN; find innovative solutions to existing and emergent challenges of patient recruitment and facilitate enhanced service delivery to sites within the ASN.

About the Role Service Delivery & Expansion
  • Manage the identification, outreach, recruitment and onboarding of high quality, high performing sites into the North America ASN
  • Develop strong relationships with high priority sites & partners through virtual or face‑to‑face meetings and conference attendance (travel required) to expand the ASN
  • Build a deep understanding of the challenges of clinical research for sites in GI and how these challenges impact recruitment and research operations
  • Maintain and deliver accurate, real‑time analytics on our ASN sites
  • Drive site recruitment in new and existing therapeutic areas and geographies
Innovation and Development
  • Build solutions to establish and grow a pipeline of high potential sites that are starting in, or naïve to, clinical research
Develop a holistic site engagement and support model
  • Oversee the development and maintenance of an Investigator portal to enhance communication and onboarding of clinical sites to the ASN and clinical studies
  • Support novel strategies for patient identification and engagement in partnership with ASN sites
Operations
  • Build stakeholder engagement and collaboration through the adoption of change management methodologies and a strong focus on building key relationships
  • Develop processes and workflows to support a scalable and growing ASN platform
  • Drive and support (cross) departmental improvement initiatives to ensure company end‑to‑end processes and technologies are efficient and effective, work seamlessly together and deliver improved customer value
  • Present and/or participate in specialized conferences/meetings to increase knowledge as needed
  • Support contract negotiations as required
About You Must have
  • 7-9 years of related experience in the clinical research industry (CRO, sponsor, SMO, or investigative site) & at minimum, an honour's Bachelors Degree (ideally; Life Sciences, Health Sciences, Nursing, Pharmacy, or a related discipline
  • Experience developing and managing relationships with investigative sites, principal investigators, and site personnel.
  • Strong understanding of the clinical trial lifecycle, including site feasibility, study startup, patient recruitment, and ICH‑GCP/regulatory requirements.
  • Excellent relationship management, communication, and influencing skills, with the ability to engage investigators, site personnel, and cross‑functional stakeholders.
  • Experience using data and performance metrics to identify opportunities, strengthen site partnerships, and improve study delivery.
  • Experience in gastroenterology or inflammatory diseases is an asset

$97,500 - $163,000 a year

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