Site Management Associate - Ciudad de México - ICON plc

ICON plc

Empresa verificada

Ciudad de México

hace 2 semanas

Publicado por:

Rodrigo Fernández

Reclutador de talento para beBee

Descripción

Summary:

The Site Management Associate is responsible for managing, implementing and monitoring clinical studies, with support, in a team setting according to ICON SOPs, SSPs and all applicable rules and regulations.

The responsibilities of this position include, but are not limited to: identifying, training/initiating and closing out study sites; conducting remote site monitoring visits and/or targeted on-site visits as needed, conducting remote site management activities, managing study sites and the required protocols, amendments and/or deviations, assuring that data is reported accurately and timelines are maintained.

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, multicultural, and multidisciplinary.

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.

Required Skills:

Excellent written and oral skills.
Obtained Bachelors degree in Lifescience / BS is a mandatory.
Minimum 1 to 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.

Salary:
$400, $800,000.00 per year

Ability to commute/relocate:

03900, Ciudad de México,

CDMX:
Reliably commute or planning to relocate before starting work (required)

Work Location:
Hybrid remote in 03900, Ciudad de México, CDMX

Expected Start Date: 01/05/2023