Site Management Associate I

IRE • Raleigh, NC

5d

About The Position

Site Management Associate I - Amgen NASCR ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers. We are currently seeking a Site Management Associate to join our diverse and dynamic team. As an associate at ICON, you will play a pivotal role in assisting with the design and analysis of clinical trials, interpreting complex data, and contributing to the advancement of innovative treatments and therapies.

Requirements

• Bachelor's degree in a scientific or healthcare-related field.
• Prior experience in clinical research support.
• Knowledge of clinical trial processes, regulations, and guidelines.
• Excellent organizational and communication skills.
• Ability to work collaboratively in a fast-paced environment with attention to detail.

Nice To Haves

• Experience in supporting investigator initiated studies.

Responsibilities

• Assist with operational activities related to the planning, implementation and execution of Non client Sponsored studies including Investigator Sponsored Studies (ISS), Co-operative group ISS, Collaborative and Research Development Agreements (CRADAs), Research Partner Studies (RPS), and Expanded Access (EA).
• Work with other members of the group to support the timely execution and completion of NASCR group deliverables in accordance with standard operating procedures (SOPs) and other supporting documentation.
• Track essential documents and file them to the central document repository and enter data into source systems.
• Support execution of operational metrics.
• May be involved in coordination and preparation for meetings (e.g., drafting agendas/minutes, scheduling speakers, materials collation).
• May provide support for numerous other aspects of the process (e.g., compiling documents for review submission, budget and contract generation, site initiation packet review and approval, and study close-out).
• May include creating and monitoring purchase orders, ad hoc administrative projects, and assisting with formatting of presentations.

Benefits

• Competitive base salary and performance related incentives
• Health and wellbeing programmes including medical, dental, and vision coverage where applicable
• Retirement and pension plans
• Life assurance and disability coverage
• Employee assistance programmes and wellbeing resources
• Learning and development opportunities through structured training and career pathways

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level