IHCRA (In-House Clinical Research Associate)

ICON plc; Michigan; Remote; USD 60,000 - 80,000; Full time

Job summary

Join ICON plc as an In-House Clinical Research Associate, where you will manage and monitor clinical studies in a dynamic remote team environment. This role requires a Bachelor's degree in a relevant field, strong organizational skills, and a background in clinical research. Enjoy a competitive salary and a comprehensive range of benefits designed to promote well-being and work-life balance. ICON values diversity and is committed to providing an inclusive workplace for all.

Benefits

Various annual leave entitlements

Health insurance offerings

Competitive retirement planning

Global Employee Assistance Programme

Life assurance

Qualifications

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

Responsibilities

• Managing study sites according to ICON SOPs.
• Preparing and submitting regulatory documents.
• Assisting in development of site and patient enrolment strategies.

Skills

Organizational skills

Communication skills

Attention to detail

Education

Bachelor's degree in life sciences or healthcare

Job description

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.
  
  

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

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