IHCRA (In-House Clinical Research Associate)

ICON plc; United States; Remote; USD 70,000 - 90,000; Full time

Job summary

ICON plc is seeking an In-House Clinical Research Associate to join their dynamic team. This role involves managing clinical studies, ensuring compliance with protocols, and coordinating study sites to advance clinical development. The ideal candidate will possess a relevant Bachelor's degree and have strong organizational and communication skills, contributing to the success of innovative healthcare solutions.

Benefits

Various annual leave entitlements

Health insurance offerings

Competitive retirement planning

Global Employee Assistance Programme

Flexible optional benefits

Qualifications

• Bachelor's degree required.
• Previous experience in clinical research preferred.
• Strong organizational and communication skills.

Responsibilities

• Manage, implement and monitor clinical studies.
• Identify, train and close out study sites.
• Ensure data is reported accurately and timelines are maintained.

Skills

Organizational skills

Communication skills

Attention to detail

Ability to work independently

Ability to work collaboratively

Education

Bachelor's degree in life sciences or healthcare

Job description

IHCRA (In-House Clinical Research Associate) page is loaded

IHCRA (In-House Clinical Research Associate)

Apply remote type Office or Home locations Regional United States (PRA) time type Full time posted on Posted Yesterday job requisition id JR132046 IHCRA (In-House Clinical Research Associate)-US-Remote

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

We are currently seeking a IHCRA (In-House Clinical Research Associate) to join our diverse and dynamic team. The In-House Clinical Research Associate is responsible for managing, implementing and monitoring clinical studies, with support, in a team setting according to ICON SOPs, SSPs and all applicable rules and regulations.

What You Will Be Doing:

• Identifying, training/initiating and closing out of study sites.
• Managing study sites and the required protocols, amendments and/or deviations, assuring that data is reported accurately and timelines are maintained.
• Assists with timely preparation and submission of regulatory documents for IRB/IEC submissions according to local requirements, with support, as needed.
• Maintains Sponsor and patient confidentiality
• Actively participates in regular meetings with Project Managers
• Assists in development of site and patient enrolment strategies with project team; works to motivate sites to meet enrolment timelines.
• Developing knowledge of and compliance with local regulatory requirements.

Your Profile:

• Bachelor's degree in a relevant field, such as life sciences or healthcare
• Previous experience in clinical research or a related field preferred
• Strong organizational and communication skills
• Ability to work independently and collaboratively in a fast-paced environment
• Attention to detail and ability to prioritize tasks effectively
• We would also Welcome some previous experience as a CRA.

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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, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised 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, subsidised 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 .

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

Are you a current ICON Employee? Please click here to apply

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