Clinical Research Coordinator

ICON Strategic Solutions; Pennsylvania; On-site; USD 45,000 - 62,000; Full time

Benefits offered by this job

Annual leave

Health insurance

Retirement planning

Employee assistance program

Life insurance

Flexible benefits

Job summary

ICON plc is seeking a Clinical Research Coordinator in McComb, MS to deliver high-standard clinical coordination work. You will collaborate with teammates and stakeholders to drive studies forward, ensure protocol compliance, and support participants throughout the trial.

The role emphasizes data integrity, regulatory knowledge, and strong communication within a dynamic team, with ICON offering comprehensive benefits and inclusive culture.

Qualifications

• Bachelor's degree in a relevant scientific discipline or healthcare-related field.
• Experience in clinical research or healthcare settings preferred.
• Knowledge of FDA/EMA regulations, ICH-GCP guidelines, and HIPAA requirements.
• Strong organizational, communication, and interpersonal skills.
• Detail-oriented with the ability to manage multiple tasks and priorities simultaneously.

Responsibilities

• Facilitate coordination and execution of clinical research studies, including participant recruitment, enrollment, and follow-up activities.
• Collaborate with principal investigators, sponsors, and regulatory authorities to ensure compliance with study protocols and regulatory requirements.
• Collect and maintain accurate clinical trial data, including adverse events, protocol deviations, and study outcomes.
• Manage study-related documentation, including informed consent forms, case report forms, and regulatory submissions.
• Provide education, counseling, and assistance to study participants regarding procedures.

Job description

Clinical Research Coordinator- McComb, MS

ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.

What You Will Do

Your role will involve delivering clinical coordination work to a high standard, working closely with your team and stakeholders.

Key Responsibilities Include

• Facilitating the coordination and execution of clinical research studies, including participant recruitment, enrollment, and follow-up activities.
• Collaborating with principal investigators, study sponsors, and regulatory authorities to ensure compliance with study protocols, regulatory requirements, and ethical standards.
• Collecting and maintaining accurate and complete clinical trial data, including documentation of adverse events, protocol deviations, and study outcomes.
• Managing study-related documentation, including informed consent forms, case report forms, and regulatory submissions.
• Providing support and guidance to study participants, including education, counseling, and assistance with study-related procedures.

Your Profile

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

Required Qualifications And Experience

• Bachelor's degree in a relevant scientific discipline or healthcare-related field.
• Previous experience working in clinical research or healthcare settings preferred.
• Knowledge of clinical research regulations, including FDA/EMA regulations, ICH-GCP guidelines, and HIPAA requirements.
• Strong organizational, communication, and interpersonal skills, with the ability to work effectively in a team environment.
• Detail-oriented with the ability to manage multiple tasks and priorities simultaneously.

What ICON Can Offer You

Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our Benefits Examples Include

• Various annual leave entitlements
• A range of health insurance offerings to suit you and your family’s needs.
• Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
• Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being.
• Life assurance
• Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.

Visit our careers site to read more about the benefits ICON offers.

At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here