Feasibility Associate

**JR104727**

**Feasibility Associate**

**Site: Mexico, Mexico City**

At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives.

Our ‘Own It’ culture is driven by four key values that bring us together as individuals and set us apart as an organization: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organization that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development.

That’s our vision. We’re driven by it. And we need talented people who share it.
If you’re as driven as we are, join us. You’ll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you’ll be helping shape an industry.

**Overview**:
The Feasibility Associate will be supporting securing the right trials for Accellacare Research sites to be successful with randomization activity and revenue generation. This role will be responsible for trial analysis and centralized feasibility processes for the Accellacare Research network.

**Responsibilities**:

- Execute effective, accurate network feasibility and deliver project proposals that maximize secured randomization opportunities for Accellacare Research within assigned therapeutic areas
- Communication skills to be able to collaborate with the Communications and Operations team to ensure trial enrollment projections are realistic and optimized.
- Conduct timely centralized follow up and provide excellent communication back to Accellacare Research sites regarding project status.
- Entry of feasibility and maintenance of key data into our CTMS systems that supports predictability, randomizations, forecasting, and other key performance measures within assigned therapeutic areas.
- Ensure proficiency and knowledge of therapeutic area expectations.
- Create files and upload appropriate documents to Clinical Conductor
- Meeting/exceeding goals set for randomizations secured by assigned therapeutic areas.
- Ensure trials are well matched as evidenced by meeting and exceeding contracted goal per assigned therapeutic areas.
- Ensure predictability of performance targets are met/exceeded within assigned therapeutic areas.
- Collaborate with Accellacare teams involved in the Study Start-Up process.
- Comply with all federal and local regulatory requirements as well as company policies.
- Travel to other sites within the network may be required.

**Qualifications**:
**You will need**:

- Desirable 1 year of experience
- Advanced English for Write / Read / and Talk
- Proficient user of the Microsoft Office Suite, particularly Excel
- Bachelor’s Degree in medicine, science or your equivalent working experience
- You should be a confident communicator, with strong client management skills and strong decision-making skills
- Clinical Trials Exp

Note: Homeworker position

**Benefits of Working in ICON**:
Our success depends on the knowledge, capabilities and quality of our people. That is why we are committed to developing our employees in a continuous learning culture - one where we challenge you with engaging work and where every experience adds to your professional development.

At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.

ICON, including subsidiaries, is an equal opportunity and inclusive employer and 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.

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