Job detail

Senior Clinical Research Associate

ICON plc

#Patient Safety #Data Integrity #Clinical Trials #ICH-GCP #Healthcare Intelligence #Clinical Research Associate #CRA #Site Monitoring #Protocol Compliance #Clinical Study Reports #Site Qualification #Medical Data Analysis

Full Time Remote Ok Remote friendly 2-5 yrsPosted 22 days ago

Location

Blue Bell, South Dakota

Quick overview

The role involves conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. It also requires ensuring protocol compliance, data integrity, and collaborating with investigators to maintain high-quality clinical data.

Requirements summary

Candidates need a bachelor's degree in a scientific or health-related field and a minimum of 1 to 3 years of independent monitoring experience depending on the level. Proficiency in ICH-GCP guidelines and the ability to travel at least 60% of the time are required.

bachelor degreeOrganizational SkillsCommunication SkillsPatient SafetyData IntegrityData ReviewProtocol ComplianceSite InitiationICH-GCP GuidelinesClinical Trial ProcessesSite QualificationQuery ResolutionClinical MonitoringStudy Documentation

Job description

Senior CRA 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.
Job Advert Posting We are currently seeking a Senior Clinical Research Associate or Clinical Research Associate II to join our diverse and dynamic team.
As a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.
What you will be doing Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.
Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
Collaborating with investigators and site staff to facilitate smooth study conduct.
Performing data review and resolution of queries to maintain high-quality clinical data.
Contributing to the preparation and review of study documentation, including protocols and clinical study reports Your profile Bachelor’s degree in a scientific or health-related field or an equivalent combination of education and clinical research experience, particularly in a study coordinator or nursing role Minimum of 1 year independent monitoring to be considered for a Clinical Research Associate II and a minimum of 3 years independent monitoring to be considered for a Senior Clinical Research Associate.
In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
Strong organizational and communication skills, with attention to detail.
Ability to work independently and collaboratively in a fast-paced environment.
Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver’s license #LI-ZH1 #LI-REMOTE 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 ICON is an award-winning workplace that enables you to make a difference to patients’ lives by being part of a world-class clinical research organisation that helps deliver new medicines & medical devices that are benefitting patients worldwide.
You are also part of a diverse company that cares about our world and is dedicated to conducting business more sustainably and supporting the communities in which we live.
If you’re as driven as we are, join us.
You’ll be working in a great environment, with some of the brightest and the friendliest people in the sector, and you’ll be helping shape an industry.
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Senior Clinical Research Associate

Quick overview

Requirements summary

Job description

Benefits

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