Senior Site Management Associate

hace 3 semanas

Ciudad de México ICON A tiempo completo

ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organizations.

With our patients at the Centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life.

Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well.

**The Role**:

- Recognize, exemplify and adhere to ICON's values which center around our commitment to People, Clients and Performance
- As a member of staff, the employee is expected to embrace and contribute to our culture of process improvement with a focus on streamlining our processes adding value to our business and meeting client needs.
- Ability to work on study teams that are often virtual, multi-cultural, and multi-disciplinary
- *Serves as the primary contact for sites and investigators participating in studies
- *Acts as a resource for internal study teams and other ICON departments
- *Maintains, reviews, and ensures adequacy of information and data contained in site management reports, tracking systems (CTMS or others) and other site management documents
- *Conducts and completes remote site management activities, with support as needed, according to applicable SOPs and the Site Management Plan
- *Participates in QA audits as needed
- *Regularly attends and contributes to project specific and departmental meetings
- *Ability and willingness to travel as needed (drive and fly) - approximately 25% of the time
- *Reviews drug storage and drug accountability procedures (as applicable), in accordance with applicable SOPs
- *Maintains and archives study documentation and correspondence, as needed
- *Assists with site contracting process, as needed

**Required Skills**:

- *Excellent written and oral skills.
- Obtained Bachelors degree in Life-science / BS is a mandatory.
- Minimum 3 years of experience into Clinical Research domain
- Strong administrative skills.
- Organisation skills to support several team members.

**Benefits of Working in ICON**:
Our success depends on the knowledge, capabilities and quality of our people. That’s 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.

LI-PD1

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