Research Study Coordinator

ICON Strategic Solutions; McComb (MS); On-site; USD 45,000 - 65,000; Full time

Job summary

ICON, a global healthcare intelligence and clinical research organization, is seeking a Clinical Research Coordinator for a 5-month onsite contract in McComb, MS. You will design and analyze trials, interpret medical data, and support the advancement of innovative treatments.

The role involves coordinating studies, ensuring regulatory compliance, managing data and docs, and assisting participants. Requires a Bachelor's in a relevant field and experience in clinical research.

Qualifications

• Bachelor's degree in a relevant scientific discipline or healthcare-related field.
• Previous experience working in clinical research or healthcare settings preferred.
• Knowledge of FDA/EMA regulations, ICH-GCP guidelines, and HIPAA requirements.
• Strong organizational, communication, and interpersonal skills.

Responsibilities

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

Skills

Clinical coordination

Regulatory compliance

Data management

Communication skills

Detail oriented

Education

Bachelor's degree in a relevant scientific discipline or healthcare-related field

Job description

Clinical Research Coordinator - 5-month contract - onsite in McComb, MS

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.

As a Clinical Research Coordinator at ICON, you will design and analyze clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.

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.

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.