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Full Time Clinical Study Start Up Jobs in Raleigh, NC

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Study Start-Up Manager

Cary, NC · On-site

Study Start-Up Manager ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven ...

Belcan

Clinical Study Manager

Durham, NC · On-site

$56.99 - $71.32/hr

Provide day-to-day study management support and oversight for assigned clinical study activities from start-up through close-out. * Coordinate with internal project team members, CROs, vendors ...

TalentBurst, Inc.

Clinical Study Manager

Durham, NC

Primary Responsibilities " Provide day-to-day study management support and oversight for assigned clinical study activities from start-up through close-out. " Coordinate with internal project team ...

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Study Start Up Associate II

Raleigh, NC · On-site

$32.50 - $44.50/hr

Study Start-Up Specialist (Sponsor Dedicated) ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

New

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Study Start Up Associate II

Cary, NC · On-site

$31 - $42.50/hr

Study Start-Up Specialist (Sponsor Dedicated) ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

New

410 ICR United States USA

Study Start Up Associate II

Cary, NC · On-site

$31 - $42.50/hr

Study Start-Up Specialist (Sponsor Dedicated) ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

New

CTI

Study Activation Manager

Raleigh, NC

Proficiency with clinical trial management systems, start-up tracking tools, and standard business ... in study start-up, site activation, clinical operations, or clinical trial management. About CTI ...

CTI

Study Activation Manager

Raleigh, NC · On-site

Proficiency with clinical trial management systems, start-up tracking tools, and standard business ... in study start-up, site activation, clinical operations, or clinical trial management. About CTI ...

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Clinical Operations Specialist

Raleigh, NC · On-site

As a Study Start Up Associate II at ICON, you will lead the initiation of clinical trials, ensuring compliance with regulatory requirements, and contribute to the advancement of innovative treatments ...

ICON

Clinical Operations Specialist

Raleigh, NC · On-site

As a Study Start Up Associate II at ICON, you will lead the initiation of clinical trials, ensuring compliance with regulatory requirements, and contribute to the advancement of innovative treatments ...

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Clinical Operations Specialist

Raleigh, NC · On-site

As a Study Start Up Associate II at ICON, you will lead the initiation of clinical trials, ensuring compliance with regulatory requirements, and contribute to the advancement of innovative treatments ...

ICON

Clinical Operations Specialist

Raleigh, NC · On-site

As a Study Start Up Associate II at ICON, you will lead the initiation of clinical trials, ensuring compliance with regulatory requirements, and contribute to the advancement of innovative treatments ...

Science 37

Site Operations Specialist

Morrisville, NC · On-site

Key responsibilities include supporting study start-up activities, maintaining and tracking clinical budget data, assisting with medical record acquisition and follow-up, coordinating logistics and ...

Science 37

Site Operations Specialist

Morrisville, NC · On-site

Key responsibilities include supporting study start-up activities, maintaining and tracking clinical budget data, assisting with medical record acquisition and follow-up, coordinating logistics and ...

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Showing results 1-20

All JobsClinical Study Start Up JobsFull Time Clinical Study Start Up JobsFull Time Clinical Study Start Up Jobs in Raleigh, NC

Full Time Clinical Study Start Up information

See Raleigh, NC salary details

$21.4K

$121.8K

$200.2K

How much do full time clinical study start up jobs pay per year?

As of Sep 4, 2026, the average yearly pay for full time clinical study start up in Raleigh, NC is $121,792.00, according to ZipRecruiter salary data. Most workers in this role earn between $82,600.00 and $152,600.00 per year, depending on experience, location, and employer.

What is the difference between Full Time Clinical Study Start Up vs Clinical Research Coordinator?

AspectFull Time Clinical Study Start UpClinical Research Coordinator
ResponsibilitiesPlanning, site selection, regulatory submissions, startup documentationParticipant recruitment, data collection, site coordination
CredentialsTypically requires a degree in health sciences or related field, experience in study startupOften requires a degree or certification in health or research, with focus on coordination
Work EnvironmentOffice-based, regulatory and planning focusSite-based, patient interaction and data management

Full Time Clinical Study Start Up professionals focus on preparing and initiating clinical trials, handling regulatory and site setup tasks. Clinical Research Coordinators primarily manage participant interactions and data collection at study sites. Both roles require related credentials but differ in daily responsibilities and work environment.

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

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

What are popular job titles related to Full Time Clinical Study Start Up jobs in Raleigh, NC?

For Full Time Clinical Study Start Up jobs in Raleigh, NC, the most frequently searched job titles are:

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The top searched job categories for Full Time Clinical Study Start Up jobs in Raleigh, NC are:

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Cities near Raleigh, NC with the most Full Time Clinical Study Start Up job openings:

Full Time Clinical Study Start Up jobs near you

Study Start-Up Manager

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Cary, NC • On-site

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 11 days ago

Job description

Study Start-Up Manager

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.


As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.


As a Manager, Study Start Up at ICON, you will lead and oversee the start-up activities for clinical trials, ensuring that all processes are completed efficiently and in compliance with regulatory requirements.

What You Will Do:

You will manage day-to-day site start-up and activation activities, supporting your team to deliver quality outcomes.
Key responsibilities include:

  • Managing and overseeing the end-to-end study start-up process, including site identification, feasibility, regulatory submissions, and site activation.
  • Leading a team of study start-up professionals, providing guidance, mentorship, and support to ensure high performance and successful project delivery.
  • Collaborating with sponsors, clinical operations, and regulatory teams to ensure compliance with local and global regulations and timelines for clinical trial initiation.
  • Monitoring study start-up metrics, timelines, and budgets to ensure projects are delivered on time and within scope.
  • Identifying potential risks and challenges in the start-up process and implementing strategies to mitigate delays or issues.
  • Driving continuous improvement initiatives to optimize the study start-up process and enhance overall efficiency.

Your Profile:

You will have solid site start-up and activation experience, with the ability to manage competing priorities and develop your team.
Required qualifications and experience:

  • Bachelor's degree in a relevant scientific discipline or healthcare-related field
  • Extensive experience in clinical trial study start-up, with a strong understanding of global regulatory requirements and clinical operations.
  • Proven leadership skills, with experience managing and mentoring teams in a fast-paced, deadline-driven environment.
  • Excellent organizational and project management skills, with the ability to handle multiple studies and priorities simultaneously.
  • Strong communication and stakeholder management skills, with the ability to collaborate effectively with sponsors and internal teams.
  • Experience with process optimization and implementing best practices in study start-up activities and the development and implementation of SSU plans
  • Willingness to travel as required (approximately 25%)

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.


Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.


Benefits may include:

  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.


Visit our careers site to read more about the benefits ICON offers.


Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.


If you require reasonable accommodations during the recruitment process, please let us know or submit a requesthere.

Are you a current ICON Employee? Please click here to apply

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