Associate Director Clinical Data Manager (all genders)

TN Germany; Darmstadt; Vor Ort; EUR 80.000 - 100.000; Vollzeit

Zusammenfassung

A leading company in the pharmaceutical industry seeks an Associate Director Clinical Data Manager in Darmstadt. This role involves overseeing clinical data management activities, ensuring data integrity, and leading a team. Candidates should have extensive experience in clinical data management and strong project management skills.

Qualifikationen

• Minimum of 10 years of experience in clinical data management.
• Proficient in contributing to non-study related initiatives.

Aufgaben

• Accountable for all Clinical Data Management related deliverables in assigned trials.
• Ensure accuracy, integrity, and completeness of clinical trial data.
• Lead process improvement initiatives in Clinical Data Management.

Kenntnisse

Project Management

Analytical Skills

Communication

Collaboration

Problem Solving

Ausbildung

Bachelor's or Master's degree in a scientific or technical discipline

Tools

Data Management Systems

Jobbeschreibung

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Associate Director Clinical Data Manager (all genders), Darmstadt

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Job Reference:

61d94d7bfce6

Job Views:

1

Posted:

13.05.2025

Expiry Date:

27.06.2025

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Job Description:

A great opportunity has opened within the Data Monitoring, Management and Innovation department to further strengthen our Clinical Data Management team.As an Associate Director Clinical Data Manager, you will play a crucial role in managing and overseeing clinical data management activities within the organization. You will be responsible for ensuring the integrity, accuracy, and completeness of clinical trial data, while also coordinating a team of clinical data management professionals in a matrix setting.Your roleAccountable for all Clinical Data Management (CDM) related deliverables in assigned global (Phase I-IIIb) trials or programs of varying complexityProvide CDM leadership for assigned trial(s)/program(s), take global accountability and serve as the CDM representative at the study/program levelDemonstrate project management and operational expertise in the strategic planning and delivery of CDM deliverables at study/program level, e.g. planning timelines and resources, risk identification and management, status tracking, internal and external stakeholder management etcDefine and execute risk-based data collection, cleaning and quality assurance strategies for eCRF and external data (including coding)Ensure the accuracy, integrity, and completeness of clinical trial data through comprehensive data review and validation activitiesEnsure quality of clinical database/deliverables (incl. eCRF and external data) as well as submission readiness of the clinical data management deliverables and data packages (e.g. CDISC)Act as primary point of contact within CDM for any HA submission related activities (e.g. preparation of briefing books, attending HA meetings as requested) Manage and oversee CRO and vendor performance, including participation in selection/assessment and budget management as required, for assigned trial(s)Contribute to the development and maintenance of data management SOPs, work instructions, and best practices.Lead process improvement initiatives and drive innovation in the field of Clinical Data ManagementAdditionally, if assigned to a program:Demonstrate good understanding of the compound profile to identify and assist in successful application of consistent CDM processes and documentation across assigned studies in an assigned program/indication e.g. ensuring consistency across data quality plansUtilise understanding of CDASH and SDTM, or other recognised industry standards, to ensure consistency of implementation across studies in assigned program/indicationMay act as a mentor for CDM colleagues within/beyond assigned programDemonstrate willingness to take on and lead any program level activity in support of study deliveryWho you areBachelor's or Master's degree in a scientific or technical discipline, preferably in life sciences, data management, or a related fieldMinimum of 10 years of experience in clinical data management within the pharmaceutical, biotechnology, or healthcare industryCommitted to continuous personal and professional development, and bringing external insights to the role to drive innovation and process improvementProficient in contributing to non-study related initiatives e.g. process improvements, in addition to study assignments Strong project management, analytical, communication, collaboration, and problem-solving skillsAbility to work proactively and independently on assigned tasks or projects of varyingcomplexity; prioritising and managing multiple activities simultaneouslyDemonstrated ability to lead and oversee end-to-end data management activities within a clinical trial, as well as leading and coordinating global teams in a matrix organizationFamiliar with autonomously providing reports to senior management, including updates on financials, forecasts and timelinesProficiency in data management systems and tools, including strong knowledge of regulatory requirements, industry standards, and best practices related to clinical data managementExperience in Risk Based Data Monitoring/Management, and with clinical trial data standards, such as CDISC, is preferredEnglish fluent