Clinical Trial Lead

ICON Strategic Solutions; France; À distance; EUR 70 000 - 90 000; Plein temps

Résumé du poste

A global clinical research company is seeking a Clinical Trial Lead for a permanent, home-based position. The ideal candidate will have over 7 years of clinical research experience, including at least 4 years in project management. Responsibilities include developing clinical trial strategies, overseeing CROs, and ensuring compliance with R&D financial standards. This role offers a dynamic environment with significant leadership responsibilities.

Qualifications

• Minimum of 7 years in clinical research, including 4 years in clinical trial management.
• Extensive experience in clinical study planning, execution, and budget management.
• Requires substantial project management experience and senior knowledge in relevant disciplines.

Responsabilités

• Lead development of clinical trial strategy and oversee execution.
• Accountable for managing CROs for Phase I – IV clinical trials.
• Prepare and present operational content at key governance discussions.

Connaissances

Clinical trial management

Project management

Vendor management

Cross-functional team leadership

Formation

BS/BA in life sciences or healthcare-related discipline

Advanced degree desirable (MPH, MS, MA, MBA, PharmD)

Description du poste

Overview

Clinical Trial Lead role at ICON Strategic Solutions. This is a permanent, home-based position on a sponsor-dedicated Pharma client. Must come from a clinical research background with at least 7 years of experience working within a Pharma or CRO, including at least 4 years as a Global CTM/Project Manager. Countries we will only consider: France, Germany, Italy, Netherlands, Poland, UK, Bulgaria.

Responsibilities

• Leads the development of the clinical trial strategy and delivers the clinical operational plan within the budget, timelines and quality standards agreed upon by Governance Committees.
• Accountable for oversight of CROs in the execution of Phase I – IV global clinical trial(s).
• Represents Global Clinical Operations (GCO) within the Global Trial Team and serves as the key GCO operational point of contact for the trial.
• Accountable for the successful preparation and presentation of operational content at key governance discussions (TARB, ICSC).
• Key contributor to the development of annual trial/project objectives and communicating to relevant line management and Clinical Operations Team.
• Drives and leads the successful execution, oversight and approval of all clinical trial documents and operational plans of global clinical trials using strong project management, leadership, and organizational skills.
• Ensures strong oversight, review and delivery of trial/project CAPAs in order to meet corporate compliance standards and timelines.
• Accountable for partnering with CRO in audit responses and addressing quality issues.
• Provides leadership and contributes to all operational aspects of the trial budget, including forecasts to ensure delivery within the R&D financial standards.
• Performs review and provides strong operational input in the development of clinical trial protocols, ICFs and CSRs and contributes as a member to the CTM Internal Protocol Review Committee.
• Filters, prioritizes, analyzes and validates complex and dynamic information from a diverse range of external and internal sources to respond to technical operational and organizational challenges.
• Supports the development and implementation of department initiatives including input on SOPs, processes, and workstreams.
• Ensures strong inspection readiness application for all assigned clinical trials.
• Cross functional management experience, leading cross functional teams
• Vendor management, leading and oversight as well as vendor budgets.

Qualifications

• BS/BA in life sciences/healthcare-related discipline or RN. Advanced degree desirable (MPH, MS, MA, MBA, PharmD); PM certification desirable.
• Minimum of 7 years in clinical research in a CRO or Pharmaceutical/Biotechnology Industry environment with at least 4 years of in-depth knowledge and experience in clinical trial management.
• Extensive experience in all aspects of clinical study planning and startup (including budget and resource planning) and in executing the complete range of clinical study activities, from startup through final study report.
• Requires substantial to extensive professional experience in relevant disciplines and substantial project management experience. Requires senior knowledge and experience in own discipline and beyond which may also require good market and competitor knowledge.
• Site and cross-functional collaboration; vendor management and budgets.

Employment type

• Full-time

Job function

• Research, Analyst, and Information Technology
• Industries: Pharmaceutical Manufacturing