Pl Vacatures in Ghent
Maak een vacature-alert aan voor deze zoekopdracht
Pl • Ghent
Data Management Lead
ArgenxGent- Gesponsord
Freelance Dotnet Developer
CegekaFlemish Brabant, Flemish Region, Belgiumoperator 3pl / 5 pl (v / x / m)
Let's WorkPetegemaandeleie.NET Developer
Versele LagaDeinze, BEOperator Chemie (2 ploegen)
JobmatchDrongen, BelgiumWMS Specialist
BleckmannWest-VlaanderenPracownik magazynowy
JOBWAY SPÓŁKA CYWILNAGhent, BelgiaElektricien (3 pl)
Accent JobsEeklo, Oost-Vlaanderen, BEOrder picker / komisjoner
InterKadra Sp. z o.o.Gandawa, Belgia- Gesponsord
Technieker 2 PL of nacht
Unique BelgiumNAZARETH, Oost-Vlaanderen, BE- Gesponsord
Erkend Milieudeskundige (M / V / X)
VinçotteLimburg, Antwerp, BelgiëFull-Stack Developer – European Commission
Edda InternationalBelgium, GhentDie Maintenance Chief
Daikin IndustriesSint-Denijs-Westrem, Oost-Vlaanderen, BEWulkanizator
Job Talent NVGent, BelgiaOperator Inpak - 2 PL
AGO Jobs & HROostakker, BEData Management Lead
ArgenxGent- Fulltime
We are currently looking for a Data Management Lead (DML) to join the Data Management team.
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 DML function may include Line Management responsibilities of a team of Clinical Data Managers (CDM).
Dependent on the program (phase and number of clinical trials) and the Line Management responsibilities, the DML may also act as CDM for 1 or more selected trials.
Roles & Responsibilities
The DML will :
- 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 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 DML will :
For the assigned trial(s) under the compound / indication, the DML will :
The DML will also participate in activities other than study-related :
Skills & Competencies
Experience & Qualifications
LI-Onsite