Physical Therapist

ICON Strategic Solutions; West Palm Beach (FL); On-site; USD 65,000 - 95,000; Full time

Benefits offered by this job

Competitive base salary

Health, dental, and vision coverage

Retirement and pension plans

Life assurance and disability coverage

Employee assistance programs and Well‑

Learning and development opportunities

Career growth opportunities

Job summary

ICON Strategic Solutions is seeking a Clinical Research Associate to join our team as a Clinical Research Associate. Travel of up to 50% is required; the role focuses on monitoring early-stage development trials (non-oncology) and collaborating with investigators to ensure protocol compliance and data integrity.

You will bring a bachelor's in a scientific or healthcare field, strong organizational and communication skills, and the ability to work independently in a fast-paced environment.

Qualifications

• Bachelor's degree in a scientific or healthcare-related field.
• Strong organizational and communication skills.
• Ability to work independently in a fast-paced environment.
• Willingness to travel up to 50% within Florida.

Responsibilities

• Conduct site qualification, initiation, monitoring, and close-out visits.
• Ensure protocol compliance, data integrity, and patient safety.
• Collaborate with investigators and site staff to facilitate study conduct.
• Perform data review and resolve queries to maintain high-quality data.
• Contribute to study documentation, including protocols and study reports.

Skills

Clinical trial monitoring

Communication skills

Organizational skills

Travel up to 50%

Education

Bachelor's degree in science or healthcare

Job description

Are you a Physical Therapist looking for a new career opportunity? We are seeking healthcare professionals to join our team as a Clinical Research Associate. This is an excellent opportunity to expand your skills, grow your career, and make an impact in clinical research. Travel of approximately 50% is required.

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

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

What You Will Do:

You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively. Focus is early-stage development clinical trials (non-oncology)

Key responsibilities include:

• 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:

You will bring relevant clinical trial monitoring experience, along with the following qualifications and skills.

Required qualifications and experience:

• Bachelor's degree in a scientific or healthcare-related field.
• Strong organizational and communication skills, with attention to detail.
• Ability to work independently and collaboratively in a fast-paced environment.
• Willingness to travel as required up to 50% within their region (Florida)

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

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 programs including medical, dental, and vision coverage where applicable
• Retirement and pension plans
• Life assurance and disability coverage
• Employee assistance programs 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.