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Remote Clinical Study Start Up Jobs (NOW HIRING)

ICON

Manager, Study Start Up

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 ...

Codera

Senior Manager, Study Start Up

San Diego, CA · Remote

Support the execution of Phase I-IV studies including study start-up, site management and clinical operations activities in compliance with principles of ICH-GCP guidelines, SOPs, local laws and ...

Emmes

Study Start-Up Associate II

Rockville, MD · Remote

$34.25 - $46.75/hr

Overview Study Start-Up Associate II US Remote Emmes Group: Building a better future for us all. Emmes Group is transforming the future of clinical research, bringing the promise of new medical ...

Intuitive

Senior Clinical Study Manager

Sunnyvale, CA · On-site +1

... start-up, and execution of clinical studies. This Lead Clinical Study Manager-4 (CSM IV) / Senior ... Perform on-site and remote site qualification visits, site initiation visits, interim monitoring ...

BeiGene, Inc.

Regional Clinical Study Manager

Generates, manages, and maintains high quality study start up and recruitment timelines for region and tracks progress towards these * Ensures that the clinical study is operationally feasible in the ...

Parexel

Senior Manager, Site Start Up

Parexel FSP has an exciting opportunity for a candidate with strong experience in Clinical Study Startup! Essential Functions Trial Start Up Group * Accountable for advancing study start-up ...

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Remote Clinical Study Start Up information

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$22K

$125.3K

$206K

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

As of Jul 25, 2026, the average yearly pay for remote clinical study start up in the United States is $125,290.00, according to ZipRecruiter salary data. Most workers in this role earn between $85,000.00 and $157,000.00 per year, depending on experience, location, and employer.

What is the difference between Remote Clinical Study Start Up vs Remote Clinical Data Coordinator?

AspectRemote Clinical Study Start UpRemote Clinical Data Coordinator
Primary ResponsibilitiesPlanning, site selection, regulatory submissions, site initiationData entry, data validation, database management, data quality assurance
Required CredentialsLife sciences degree, knowledge of GCP, regulatory knowledgeLife sciences or related degree, familiarity with clinical data systems
Work EnvironmentCollaborates with sponsors, sites, regulatory bodiesWorks mainly with data management teams and databases
Industry UsageInvolved early in trial setup phasesInvolved during data collection and analysis phases

Remote Clinical Study Start Up focuses on preparing and initiating clinical trials, including site selection and regulatory compliance. In contrast, Remote Clinical Data Coordinator manages and ensures the accuracy of clinical trial data during the study. Both roles require related credentials and work within the clinical research industry, but they operate at different stages of the trial process.

More about Remote Clinical Study Start Up jobs
What cities are hiring for Remote Clinical Study Start Up jobs? Cities with the most Remote Clinical Study Start Up job openings:
What are the most commonly searched types of Clinical Study Start Up jobs? The most popular types of Clinical Study Start Up jobs are:
What states have the most Remote Clinical Study Start Up jobs? States with the most job openings for Remote Clinical Study Start Up jobs include:
What job categories do people searching Remote Clinical Study Start Up jobs look for? The top searched job categories for Remote Clinical Study Start Up jobs are:
Remote Clinical Study Start Up jobs near you
Infographic showing various Remote Clinical Study Start Up job openings in the United States as of July 2026, with employment types broken down into 2% As Needed, 73% Full Time, 17% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $125,290 per year, or $60.2 per hour.
Manager, Study Start Up

Manager, Study Start Up

ICON

Remote

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 15 hours 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 Study Start Up Manager 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.
  • 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 request here.
Are you a current ICON Employee? Please click here to apply

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