Study Start-Up Associate II

Study Start- Up Associate II 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.

As a Study Start Up Associate II at ICON, you will lead the initiation of clinical trials, ensuring compliance with regulatory requirements, and contribute to the advancement of innovative treatments and therapies.

What You Will Do:

You will contribute to site start-up and activation activities, taking responsibility for your deliverables and working collaboratively.

Key responsibilities include: Work   directly with assigned sites on all site   related   essential document collection and review.

Assist with Country level ICD preparation.

Review and approve site level ICDs.

Partner with   internal Study Startup team , CROs, Clinical Operations teams, and TAU partners to improve overall   S SU   metrics and   deliver   processes.  

Ensure   standards are applied to the   S SU   process es   across project s .    

Review site essential documents for   start-up   including but not limited to: ICF, FDF, 1572,   CVs   etc  

Promptly recognize and improve potential   site activation   delays and escalate   to   appropriate team   members .  

Track   all   actions a nd communications with sites   to   ensure   timelines   are   achiev e d for   studies and   sites assigned .   

Support r esolv ing   escalated issues   identified   by the   CROs   and   Clinical Operations teams   in partnership with the   internal Study Startup team.  

Review and provide feedback to management on site performance metrics.  

Ensure accuracy and completeness of the eTMF for assigned sites during start up  

Your Profile:

You will bring relevant site start-up and activation experience, along with the following qualifications and skills.

Required qualifications and experience:

BS degree or international equivalent   

2   or more years of experience in   clin i cal research   Site   Start Up   within a pharmaceutical company, CRO or relevant industry vendor .  

Ability to explain data   to   facilitate   decision making processes to be data driven.  

Knowledge and u nderstanding of   clinical   study protocols and   essential documents  

Strong   organizational   skills, decision making, communication and   negotiation skills  

Proficient in Microsoft Excel, Word, and PowerPoint .  

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

Rewards & Benefits 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 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

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 .

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