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Initiation Clinical Research Associate Jobs (NOW HIRING)

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About the Opportunity As a Clinical Research Associate within our sponsor-dedicated environment ... Conduct site qualification, initiation, routine monitoring, and close-out visits * Ensure protocol ...

CTTX Health

Clinical Research Associate

Cambridge, MA · On-site

... looking for a Clinical Research Associate (CRA) to join a fast-growing biotech company ... Conduct site initiation, monitoring, and close-out visits to ensure trials meet the highest quality ...

Medasource

$70 - $75/hr

Sr. Field Clinical Research Associate Remote with Travel required in the North Central Region ... You will play a key role in site initiation, periodic and close-out visits, data and documentation ...

BD Mexico

The Clinical Research Associate (CRA) is responsible for the management and monitoring of assigned ... Conduct monitoring activities, including qualification, initiation, routine monitoring, and ...

North American Science Associates, Inc.

$100K/yr

May conduct on-site and remote site qualification, site initiation, interim, and site close-out ... Certifications such as Society of Clinical Research Associates (SoCRA) or Association of Clinical ...

Becton, Dickinson and Company

Facilitate site initiation visits and support the development and delivery of site-facing training and presentation materials. * Identify, communicate, and help resolve study risks, issues, and ...

CTTX Health

Clinical Research Associate

Cambridge, MA · On-site

... looking for a Clinical Research Associate (CRA) to join a fast-growing biotech company ... Conduct site initiation, monitoring, and close-out visits to ensure trials meet the highest quality ...

BioTalent

We are seeking an experienced Senior Clinical Research Associate (CRA) to independently manage and ... Site Initiation Visits (SIVs) * Interim Monitoring Visits (IMVs) * Close-Out Visits (COVs) * Serve ...

Pfizer

Senior Clinical Research Associate I

The Senior Clinical Research Associate I is responsible for the site management, site monitoring ... Conduct onsite, remote/electronic monitoring as needed for study site initiation, routine ...

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Initiation Clinical Research Associate information

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How much do initiation clinical research associate jobs pay per hour?

As of Sep 15, 2026, the average hourly pay for initiation clinical research associate in the United States is $41.13, according to ZipRecruiter salary data. Most workers in this role earn between $28.85 and $52.64 per hour, depending on experience, location, and employer.

What is an initiation clinical research associate?

Initiation Clinical Research Associates (ICRAs) are specialized professionals in clinical research who focus on the start-up phase of clinical trials. Their main responsibilities include coordinating regulatory document collection, reviewing site contracts, and ensuring all essential documents are in place before a clinical trial begins. ICRAs act as a liaison between the sponsor, study sites, and regulatory bodies to ensure that regulatory and ethical requirements are met. They play a critical role in preparing sites for study activation and ensuring a smooth transition to the next phases of the trial.

What are the key skills and qualifications needed to thrive as an initiation clinical research associate?

To thrive as an Initiation Clinical Research Associate, you need a solid understanding of clinical research protocols, regulatory requirements, and a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), electronic trial master files (eTMF), and GCP certification are typically required. Strong organizational skills, attention to detail, and effective communication are essential soft skills for coordinating with study sites and sponsors. These competencies are crucial for ensuring regulatory compliance, timely study start-up, and smooth collaboration across project stakeholders.

What are some common challenges faced by initiation clinical research associates during study start-up, and how can they be managed?

Initiation Clinical Research Associates (ICRAs) often encounter challenges such as delays in regulatory approvals, contract negotiations, and site readiness during the study start-up phase. Managing these obstacles typically involves proactive communication with study sites, close collaboration with regulatory and legal teams, and thorough follow-up on outstanding documents or tasks. Effective time management and adaptability are crucial, as priorities can shift rapidly. Building strong working relationships with site staff and internal teams can also help streamline processes and resolve issues efficiently.

What is the difference between Initiation Clinical Research Associate vs Clinical Research Associate?

AspectInitiation Clinical Research AssociateClinical Research Associate
Primary FocusSite initiation, startup activities, and protocol implementationMonitoring, data collection, and site visits throughout the study
Work EnvironmentPre-study setup, often in offices or at sites during startupOngoing site monitoring at multiple locations
Required CredentialsBachelor's degree, clinical research training, possibly certificationBachelor's degree, clinical research training, possibly certification

Initiation Clinical Research Associates focus on site startup activities, ensuring sites are prepared for study commencement, while Clinical Research Associates primarily monitor ongoing study progress. Both roles require similar credentials and work in the clinical research industry, but their responsibilities differ based on the study phase.

What cities are hiring for Initiation Clinical Research Associate jobs?

Cities with the most Initiation Clinical Research Associate job openings:

What states have the most Initiation Clinical Research Associate jobs?

States with the most job openings for Initiation Clinical Research Associate jobs include:

What are popular job titles related to Initiation Clinical Research Associate jobs?

For Initiation Clinical Research Associate jobs, the most frequently searched job titles are:

Initiation Clinical Research Associate jobs near you

Clinical Research Associate II / Senior Clinical Research Associate

Raleigh, NC • On-site, Remote

410 ICR United States USA
See more jobs at 410 ICR United States USAexternal

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 17 days ago

Job description

North America | Remote | Sponsor-Dedicated (FSP) Opportunities

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.


At ICON Strategic Solutions, we're continually growing our network of talented Clinical Research Associates across North America. As we expand our partnerships with leading global sponsors, we are seeking experienced CRA II and Senior CRA professionals interested in sponsor-dedicated opportunities.

About the Opportunity

As a Clinical Research Associate within our sponsor-dedicated environment, you will play a critical role in the successful delivery of clinical trials, helping bring innovative therapies to patients worldwide.

Depending on your experience level, you may:

  • Conduct site qualification, initiation, routine monitoring, and close-out visits
  • Ensure protocol compliance, patient safety, data quality, and regulatory adherence
  • Build strong relationships with investigative sites and key stakeholders
  • Identify and proactively resolve site and study issues
  • Collaborate with cross-functional teams to support successful study delivery
  • Support inspection readiness and high-quality study execution
  • Mentor and guide less experienced CRAs (Senior CRA level)

What We're Looking For

CRA II

  • Bachelor's degree in a scientific, healthcare, or related field
  • Clinical monitoring experience within the pharmaceutical, biotech, or CRO industry
  • Strong knowledge of ICH-GCP, clinical trial regulations, and monitoring practices
  • Ability to work independently while collaborating effectively across teams

Senior CRA

  • Significant clinical monitoring experience across multiple studies and sites
  • Advanced knowledge of clinical trial processes, regulations, and site management
  • Proven ability to manage priorities and drive study quality independently
  • Experience mentoring or supporting other CRAs is advantageous

For all applicants

  • Strong communication and relationship-building skills
  • Willingness to travel as required
  • Passion for advancing clinical research and improving patient outcomes

When you join ICON Strategic Solutions, you gain the best of both worlds:

  • Work within dedicated sponsor environments
  • Build expertise with leading global pharmaceutical and biotechnology companies
  • Access diverse opportunities across multiple therapeutic areas
  • Benefit from ICON's global scale, career development, and support network
  • Join a culture focused on innovation, collaboration, and patient impact
  • Competitive compensation and benefits package

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