Medical Affairs Specialist

Job Title: Medcial Affairs Specialist

Location: Mexico City, Mexico

At ICON, it's our people that set us apart.

As a global provider of drug development solutions, our work is serious business. But that doesn't mean you can't have fun while you do it. With our vision to be the partner of choice in drug development, we hire only the best and brightest in the industry! Are you one of them?

At ICON, we have an incredible opportunity for a Medical Affairs Specialist to join the team in our Warsaw office,

This is a fabulous role within our Medical Affairs team that offers a phenomenal view of the life cycle of a clinical trial. You will be part of a wider project team and have great exposure to both internal and external customers.

In this role you will provide support to Medical Affairs management and Medical Monitors in all aspects of Medical Affairs activities, as needed. Assist in providing medical/scientific consultation to our customers.

Role

• Demonstrate meaningful protocol and product knowledge of assigned protocols with mentorship from the Medical Monitor
• Author and contribute to the preparation of core MA deliverables
• Recognize potential issues relevant for Medical Affairs project tasks and escalate according to the applicable procedure - own it!
• Perform review of clinical and diagnostic data with oversight from the MM as it relates to patient safety
• Liaise with investigational site and/or Sponsor as necessary regarding MA issues with oversight and guidance from MM
• Liaise with safety and regulatory teams in order to facilitate open communication regarding updates on SAEs and regulatory issues

Requirements

• Bachelor's Degree or local equivalent Medical or Health-Science background (nursing preferred
• Prior relevant clinical research experience
• Demonstrates professional demeanour, judgment, and discernment in interactions with colleagues, clients and other ICON staff
• High level of flexibility and ability to prioritize one's own work and others as it relates to the overall processes
• Basic knowledge of medical terminology and coding systems
• Ability to analyze data in a broader context as it applies to the review of clinical trial data (laboratory values, eCRF, listings, coding) with guidance from Sr. MA Specialist, MA Coordinator
• Proficient English verbal and written communications

Benefits of Working in ICON:
Our success depends on the quality of our people. That's why we've made it a priority to build a culture that rewards high performance and nurtures talent.

We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals - both ours and yours.
We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans - and related benefits such as life assurance - so you can save and plan with confidence for the years ahead.
But beyond the competitive salaries and comprehensive benefits, you'll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change.

ICON 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.
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 through the form below.