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Remote Clinical Study Start Up Jobs (NOW HIRING)

Senior Clinical Trial Manager

Blue Bell, PA ยท On-site +1

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Senior Clinical Trial Manager, Biotech - Remote, US ICON is a global healthcare intelligence and ... Timely Study Start-Up & Enrollment: Drive enrollment and lead study start-up activities, adhering ...

We are open to remote work within the US for the right candidate. CORE ACCOUNTABILITIES Specific ... Lead selection and performance management of CROs and other ancillary vendors during study start-up ...

Clinical Operations Associate (Pool)

CA ยท Remote

$70K - $80K/yr

  • Medical

  • Retirement

  • PTO

Vanguard Clinical, Inc. is a Contract Research Organization (CRO) headquartered in San Diego, CA ... Study Start-Up (SSU) Support * Support collection, tracking, and review of essential documents ...

Clinical Operations Specialist (Pool)

CA ยท Remote

  • Medical

  • Retirement

  • PTO

Vanguard Clinical, Inc. is a Contract Research Organization (CRO) headquartered in San Diego, CA ... Study Start-Up (SSU) Support * Independently manage essential document collection, QC, and ...

Senior Clinical Study Manager (CSM)

Cleveland, OH ยท Remote

$60 - $80/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Remote - offsite Joule is current looking to hire aSenior Clinical Study Manager (CSM) to support clinical programs focused on cell/gene therapy and oncology for one of our clients. This is a remote ...

Senior Clinical Study Manager (CSM)

Cleveland, OH ยท Remote

$60 - $80/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Remote - offsite Joule is current looking to hire aSenior Clinical Study Manager (CSM) to support clinical programs focused on cell/gene therapy and oncology for one of our clients. This is a remote ...

... the study lifecycle by developing and managing regulatory and start-up project plans; coordinating and submitting Clinical Trial Applications (CTAs) to all applicable regulatory bodies (Ethics ...

Showing results 41-60

Remote Clinical Study Start Up information

See salary details

$22K

$125.3K

$206K

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

As of Aug 15, 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.

Can you do clinical research virtually?

Remote clinical study start-up roles can involve virtual work, especially with the increasing use of digital tools and electronic data capture systems. Many tasks, such as site identification, regulatory document preparation, and communication with study sites, can be performed remotely, though some activities may require in-person visits or site monitoring. Strong organizational skills and familiarity with remote collaboration platforms are important for success in virtual clinical research roles.

How to start a career in remote clinical study start up?

To start a career in remote clinical study start-up, gain relevant education such as a degree in life sciences, healthcare, or related fields, and develop knowledge of clinical trial processes and regulations. Experience with project management tools, good communication skills, and understanding of regulatory requirements like GCP are valuable. Entry-level roles often require certification or training in clinical research, and remote work may demand strong organizational skills and self-motivation.

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:

Infographic showing various Remote Clinical Study Start Up job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 64% Full Time, 16% Part Time, and 19% Contract. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution, with an average salary of $125,290 per year, or $60.2 per hour.

Senior Clinical Trial Manager

Icon plc

Blue Bell, PA โ€ข On-site, Remote

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted yesterday


Job description

Senior Clinical Trial Manager, Biotech - Remote, US

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 Senior Clinical Trial Manager at ICON, you will manage clinical trial operations activities, supporting your team and stakeholders to deliver high-quality outcomes across our clinical programmes.

What You Will Do:

Your focus will be on coordinating clinical trial management delivery, resolving issues, and developing team capability.
Key responsibilities include:

  • Budget Oversight Oversee the clinical portion of the budget to ensure efficient resource allocation.
  • Ensuring Effective Study Oversight: Develop monitoring plans and tools, ensuring effective study oversight.
  • Optimizing Performance: Train and mentor Clinical Research Associates (CRAs) to optimize their performance.
  • Timely Study Start-Up & Enrollment: Drive enrollment and lead study start-up activities, adhering to timelines.
  • Improving Study Integrity Review trip reports and implement corrective and preventative action plans when necessary.Building Productive Relationships: Foster productive relationships with Sponsors, vendors, and cross-functional teams.

Your Profile:

You will have solid clinical trial management experience, with the ability to manage competing priorities and develop your team.
Required qualifications and experience:

  • A minimum of 4+ years of experience in a Clinical Trial Management position at a CRO or Pharmaceutical Organization.
  • Bachelor's degree in health, life sciences, or other relevant fields of study.
  • At least 10+ years of relevant experience in clinical trial management.
  • Preferred: 2+ years of monitoring experience.
  • Experience in managing complex or global trials is advantageous.
  • Preferred: Experience in managing all trial components from start-up to database lock.
  • Preferred: Experience in coaching/mentoring other CTMs, leading a team of CTMs, and participating in departmental initiatives.
  • 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