Lead, Trial Delivery Manager, Oncology (5 Openings)

• Job titleLead, Trial Delivery Manager, Oncology (5 Openings)
• FunctionR&D Operations
• Sub functionClinical Trial Project Management
• CategorySenior Analyst, Clinical Trial Project Management (P6)
• LocationBeerse / Porto Salvo / Neuss / Issy-Les-Moulineaux / Madrid / Warsaw / Milano / Leiden / Solna / Belgium / Portugal / Germany / France / Spain / Poland / Italy / Netherlands / Sweden
• Date postedJul 02 2025
• Requisition numberR-021697
• Work patternHybrid Work

• Job Function:

  R&D Operations

  Job Sub Function:

  Clinical Trial Project Management

  Job Category:

  Professional

  All Job Posting

Purpose:

The Lead, Trial Delivery Management (TDM) is responsible for the execution of study-level activities, creating and updating trial-specific documents, vendor oversight & delivery, compound training, and other activities. The TDM is responsible for country and regional oversight of local operational delivery,

including the alignment of the feasibility strategy and target setting, risk reviews and local challenges that could impact overall study delivery.

Primary Responsibilities:

• Create and update critical trial-specific documents (e.g., Monitoring Guidelines, Informed Consent Form, Investigational Medicinal Product [IMP] related documentation).
• Manage vendor set up and management of day-to-day study vendor activities, including set-up, SOW creation and budget oversight.
• Responsible for country / regional coordination of trial management activities and oversight (e.g., aligns feasibility strategy with local teams, perform country-level risk reviews, aware of all projects conducted across countries).
• Support development of program-level compound training, collaborating with Clinical / CTL&T / Medical writing.
• Provide input into trial level operational strategies.
• Resolve trial-related issues and mitigate trial-related risks.
• Participate in process improvement activities at a trial, compound & cross-DU level, as needed.
• Provide support during Health Authority inspections and on the identification of risks and mitigation plans at the program level for key issues.
• Mentor & support onboarding of new team members, particularly those in Trial Management.

Principal Relationships:

• Internal: Trial Management Directors, Clinical Trial Leaders, Clinical Trial Assistants, Representatives of Delivery Operations, representatives of other GD Functions and Clinical Teams, representatives of Procurement

Qualifications / Requirements:

• BS degree or equivalent, preferred areas of study include Life Sciences (Life Sciences (e.g., Biology, Chemistry, Biochemistry, Nursing, Pharmacy).
• Minimum of 4 years clinical trial experience in Pharmaceutical, Healthcare or related industries.
• Clinical research operational knowledge and experience across multiple phases of studies (Phase I-IV); must have the ability to manage multiple aspects of execution of a clinical trial.
• 2-3 years’ experience supporting multiple aspects of a global clinical trial.
• Minimum of 2 years of oncology clinical trial experience.
• Must possess excellent leadership skills and proven ability to foster team productivity and cohesiveness.
• Experience leading without authority and in muti-functional matrixed and global environments.
• Excellent decision-making, analytical and strong financial management skills are essential to this position.
• Operate and execute with limited supervision.
• Experience mentoring/coaching others.
• Strong project planning/management, (e.g. organization, problem-solving, and adaptability) communication (e.g. effective communication with and managing expectations of stakeholders) and presentation skills are required.
• Ability to think strategically and work through ambiguous situations.
• Ability and experience to lead the Study Management Meetings.
• Experience and skills utilizing technology (e.g. tools, systems with GenAI enabled capabilities) to obtain reports for efficient metric oversight.
• Travel up to 15-20% of the time, defined by business needs.