Data Management Lead

Argenx; Oost-Vlaanderen; Presencial; EUR 90.000 - 120.000; Jornada completa

Descripción de la vacante

argenx is seeking a Clinical Data Management Lead (CDML) to drive data management across assigned compounds and indications. You will partner with CROs and internal teams to establish data management expectations, standards, and timelines aligned with a strong clinical development strategy.

You will oversee the clinical data portfolio, budgets, and regulatory readiness, mentor CDMs, and ensure high-quality data deliverables from trial initiation through close-out.

Formación

• Lead Data Management efforts across compounds/indications coordinating with CROs and internal teams.
• Oversee development and management of the Clinical Data Plan (CDP) and budget for assigned indications.
• Ensure compliance with SOPs and regulatory requirements from trial start-up to close-out.

Responsabilidades

• Lead the Data Management function for the assigned compound/indication, aligning CROs and internal partners.
• Oversee CRO selection, contracting, and oversight for data management activities.
• Contribute to protocol development relevant to Data Management (feasibility, data collection, interim locks).
• Oversee outsourced Data Management deliverables (SOW, data collection tools, DMP, UAT, archival packages).
• Ensure data management documents are prepared timely and of high quality to support trial conduct and data quality.
• Monitor project plans, budgets, metrics and KPIs; adjust plans with the Head of Data Management and stakeholders.
• Line manage CDMs, onboard new staff, and ensure training is documented.
• Share learnings and best practices across indications and departments.

Descripción del empleo

Join us as we transform immunology and deliver medicines that help autoimmune patients get their lives back. argenx is preparing for multi-dimensional expansion to reach more patients through a rich pipeline of differentiated assets, led by VYVGART, our first-in-class neonatal Fc receptor blocker approved for the treatment of gMG, and with the potential to treat patients across dozens of severe autoimmune diseases.

We are building a new kind of biotech company, one that maintains its roots as a science-based start-up and pushes our commitment to innovate across all corners of our business. We strive to inspire and grow our company, our partnerships, our science, and our people, because when we do, we deliver more for patients.

The DML is accountable for all Data Management aspects of the assigned compound and/or indication from initiation till closure of activities ensuring that clinical data completeness, accuracy and consistency meet the standards of quality for analysis and reporting to regulatory bodies, compliant with the local and global regulations. The CDML function includes Line Management responsibilities of a team of Clinical Data Managers (CDM).

Roles and Responsibilities:

• Take a leadership role with the CRO and other internal and external partners to establish, align and conform Data Management expectations for the assigned compound and/or indication
• Take a leadership role for Data Management in the Clinical and indication Team, which is ultimately responsible to define the clinical development strategy supporting the Target Product Profile (TPP) across the lifecycle of a compound, starting with the preparation of the "First-in-Human" (FiH) clinical trial throughout "Registration" and post-approval clinical development activities
• Participate in the creation and maintenance of the Clinical Development Plan (CDP) which is describing the clinical development strategy, comprising effective where possible innovative trial designs
• Oversee risk identification and risk mitigation strategies for the CDP. Identify risks or deviations from plans and communicate to the Head of Data Management; to the responsible Program Leader (PL) and Management as appropriate, proactively provide solutions and oversee implementation
• Set quality expectations and timelines for Data Management deliverables and will regularly follow up on Data Management milestones. Ensure inspection readiness at all times
• Ensure compliance with SOPs, company policies and regulatory requirements from trial start-up to trial close-out
• Set expectations, communicate in a transparent, clear way and motivate team members to work towards achieving the clinical goals in line with the OGSM and the cultural pillars

For the assigned compounds/indication(s) the CDML will:

• Oversee the CRO selection and contract negotiations
• Support the Clinical Data Portfolio Lead in keeping the oversight of the clinical budget for the assigned indication/program, collaborate with the CDMs andStatisticians to make sure the budgets are prepared, reviewed and updated within the forecast timelines as agreed with the PL and finance. Ensure that the trials and assigned clinical activities are executed within the agreed budget. Pro-actively escalateto the PL
• Contribute to development of the protocol for the sections relevant for Data Management (feasibility of data collection, adherence to industry and argenx standards, (interim) locks) and/or review of protocol versions

For the assigned trial(s) under the compound/indication, the CDML will:

• Ensure oversight of all deliverables of activities outsourced to CROs as outlined in the SOW and described in the Data Management Trial Oversight plan, including, but not limited to:
• Creation of data collection tools (EDC, DTAs for 3rd party vendors, EDC integrations)
• Creation of essential documents (DMP, UAT documents)
• Creation of submission ready clinical data package per regulatory agencies requirements
• Creation of archival package of clinical data per argenx requirements
• Ensure oversight of all activities related to Data Management:
• Ensure that Data Management essential documents are written in a timely manner and of such quality to allow the evaluation of the conduct of a trial and the quality of the data produced
• Keep track of project plan, budget, metrics and KPIs. Adjust project plan as needed in consultation with Head of Data Management, CDM, Data Management CRO and Clinical Team as appropriate
• Ensure consistency between trials on compound/indication level
• Leverages learnings and shares best practices within the indication and department

The CDML will also participate in activities other than study-related:

• Lead/participate in initiatives on process improvements
• Participate in regulatory inspections and company audits
• Line Management of CDMs and full on-boarding of new direct reports
• Ensure that assigned staff is adequately trained and that training is documented
• Mentor and enable the growth and development of assigned sta