Global Site Management Lead (all genders)

at  AbbVie

Hessen, Hessen, Germany -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate13 Jun, 2024Not Specified14 Mar, 2024N/AGood communication skillsNoNo
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Description:

What makes you stand out, makes you ready to make an impact. At AbbVie
Science is at the heart of what we do. People are at the heart of why we do it.
Welcome to AbbVie! As part of an international company with 50,000 employees worldwide and around 3,000 employees in Germany, you will have the opportunity of addressing some of tomorrows unmet medical needs in close collaboration with your colleagues. Are you passionate about improving global health care? Do you want to contribute to improving patients’ quality of life through your expertise? In a challenging work environment that offers opportunities of developing and increasing your own skills? You’ve come to the right place!
In our Clinical, Site Management and Monitoring department within Research and Development, you will be working in a team of talented people and experienced experts toward developing tomorrow’s products. In cutting-edge laboratories, you will be setting highest standards in the competitive field.

Responsibilities:

  • Develops and Drives operational study-level strategy to be executed by CSM Country teams, including risk identification, evaluation, and mitigation to establish alignment with overall study execution. Identifies risk to CSM deliverables and effectively communicates them within CSM (global, area and regional level) and to the Core Study Team. Manages identified risk through development of effective mitigation and action plans at study-level. Works with ASML, Country Leaders and other functional areas, as appropriate, to drive implementation of mitigation and action plans.
  • Member of the Core Study Team, representing CSM globally from study planning through study closeout. Actively contributes to planning and execution of the clinical programs including content of the protocol and study plans (e.g. IDRP, RAMP, Recruitment Strategy and Plan). Provides input into vendor selection and content of site-facing vendor platforms.
  • Accountable for CSM study execution and oversight of timeline development and adherence through the study lifecycle. Includes working with CSM country leadership to ensure LBEs meet overall study timelines and, if not, establishing a risk mitigation plan for discussion with the study team and ensuring all participating countries are informed and aligned to the overall timelines for the study.
  • Partners with stakeholders (Clinical Study Leadership, Study Performance & Delivery, CTRG, DSS, CDSM and CSM Country leaders, etc.) in developing overall study planning for CSM deliverables and dependencies, using analytics and country intelligence to enhance the Country and Site selection process. Ensures CSM Country leaders receive appropriate and timely study information, documentation and tools to allow for plans to be executed as per targeted milestones.
  • Accountable for driving site management activities from study start-up through study closeout ensuring delivery of site selection/activation, subject recruitment, protocol compliance, data quality and adherence to monitoring plan.
  • Provides the perspective of the CSM organization, investigators, and patients, for the development of study documents, including, as applicable, CRA training delivery plans and materials, site staff and patient facing material.
  • Accountable for site-level risk assessments, risk mitigation execution and remediation of site-level non-compliance.
  • Serves as the CSM SME for inspection readiness, ensuring study and site inspection readiness at all times. Assists with audit responses, as applicable.
  • Accountable for the development of the study monitoring plan (SMP) and delivers SMP related training. Provides CSM input on study-specific CRA training plans and training materials, site staff and patient facing materials.
  • Has input on day to day activities of assigned ASML(s) via matrix reporting
  • Leads change management in the adoption of new technologies and processes in the assigned study(ies) conduct to support consistency and operational excellence in CSM overall execution. Develops global CSM lessons learned for the assigned study(ies)with appropriate stakeholders. Shares and implements best practices within CSM. Contributes to improving CSM efficiency, which may include participating in Continuous Improvement Initiative(s).
  • When applicable, responsibilities include participating in the vendor selection process and managing clinical site management vendors. Accountable for supervising CRO oversight and issue escalation related to CRO monitoring activities.
  • Bachelor’s Degree or equivalent OUS degree, typically in (para)medical or scientific field.
  • A minimum of 5 years + of industry clinical research experience including 1 year of monitoring or project management or equivalent experience on a global study.
  • Preferred exposure in study initiation through study completion in multiple phases of studies (Phase II and III, Phase I in patients). Experience in multiple therapeutic areas or disease state/indications highly desired.
  • Demonstrates a high level of core and technical competencies through management of various components of clinical trials.
  • Possesses good communication skills and demonstrated leadership abilities. Able to influence without authority in a matrix environment.
  • Competent in application of standard business procedures (Standard Operating Procedures, International Conference on Harmonization (ICH), Global Regulations, Ethics and Compliance).
  • Demonstrated good written and verbal communication skills including fluency in English. Excellent planning and organizational skills and the ability to work effectively and efficiently in a dynamic, fast-paced environment.
  • Able to work well within a team and autonomously. Thinks proactively.


REQUIREMENT SUMMARY

Min:N/AMax:5.0 year(s)

Pharmaceuticals

Pharma / Biotech / Healthcare / Medical / R&D

Clinical Pharmacy

Graduate

(para)medical or scientific field

Proficient

1

Hessen, Germany