Clinical Research Physician
Site: 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:
Provide medical support to ICON Project Teams in order to ensure that projects of all phases (1-4) are conducted according to the highest ethical principles and medical standards, in accordance with good pharmacovigilance practices and in compliance with applicable legal and regulatory standards
Responsibilities:
The role:
*Responsible for medical data review of patients participating in assigned clinical trials
*Adverse event reporting to the sponsor
*Provide support to Medical Monitor.
*Communication of safety issues to the head of the department or designee
*Participate in the on-call system for providing 24/7 medical support
*Provide all necessary medical support functions as defined by project specific contractual obligations which will include, but not be limited to, the following:
*Partnering with Medical Affairs Specialist to ensure patient data integrity.
*Contribute to investigator meeting presentations in partnership with Medical Monitors
*Ongoing safety review of individual patient laboratory reports generated by central laboratories *CRF safety review
*Contribute any necessary medical input into integrated clinical and statistical reports
*Identify areas of concern with data and escalate as needed.
*Demonstrate a thorough understanding of ICON Standard Operating Procedures (SOPs) and ensure that all activities are conducted in accordance with current SOPs
*Demonstrate a thorough understanding of applicable regulatory standards in the country where clinical studies are to be conducted and ensure that all activities are conducted in compliance with current regulations
*Keep the person to whom the Clinical Research Physician reports informed of any issues within the department which require attention
*May be responsible for helping to provide Medical Monitoring support on occasion.
Qualifications:
• A Minimum of 2 years of experience in a clinical capacity. Clinical Research experience is a huge plus.
• Doctorate (Medical) degree
• Ability to medically evaluate clinical data
• Advanced English for Reading, Writing and Speaking
• Excellent written and verbal communication
*Strong MS Office Skills
*Ability to work both independently and in a team setting.
- Note: Office-Based Position to start. Will move to Hybrid Position (2 days at home, 3 days at the office) after training period.
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
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